House mouse: Difference between revisions
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{{Short description|Species of mammal}} | {{Short description|Species of mammal}} | ||
{{Use dmy dates|date=June 2025}} | |||
{{Speciesbox | {{Speciesbox | ||
| image = Мышь 2.jpg | | image = Мышь 2.jpg | ||
| status = LC | | status = LC | ||
| status_system = IUCN3.1 | | status_system = IUCN3.1 | ||
| status_ref = <ref name=IUCN>{{cite iucn |author1=Musser, G. |author2=Hutterer, R. |author3=Kryštufek, B. |author4=Yigit, N. |author5=Mitsainas, G. |year=2021 |title=''Mus musculus'' |amends=2016 |page=e.T13972A197519724 |doi=10.2305/IUCN.UK.2021-1.RLTS.T13972A197519724.en |access-date=17 February 2022}}</ref> | | status_ref = <ref name=IUCN>{{cite iucn |author1=Musser, G. |author2=Hutterer, R. |author3=Kryštufek, B. |author4=Yigit, N. |author5=Mitsainas, G. |year=2021 |title=''Mus musculus'' |amends=2016 |page=e.T13972A197519724 |doi=10.2305/IUCN.UK.2021-1.RLTS.T13972A197519724.en |access-date=17 February 2022 }}</ref> | ||
| genus = Mus | | genus = Mus | ||
| parent = Mus (Mus) | | parent = Mus (Mus) | ||
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| authority = [[Carl Linnaeus|Linnaeus]], [[10th edition of Systema Naturae|1758]] | | authority = [[Carl Linnaeus|Linnaeus]], [[10th edition of Systema Naturae|1758]] | ||
| subdivision_ranks = Subspecies | | subdivision_ranks = Subspecies | ||
| subdivision = *''[[Mus musculus bactrianus]]''<ref name=Lawal1>{{cite journal |last1=Lawal |first1=R.A. |display-authors=etal |year=2022|title=Taxonomic assessment of two wild house mouse subspecies using whole-genome sequencing |journal= Scientific Reports |volume=12 |issue= 20866 |page=20866 |doi= 10.1038/s41598-022-25420-x |doi-access=free |pmid= 36460842 |pmc=9718808 |bibcode=2022NatSR..1220866L }}</ref> | | subdivision = * ''[[Mus musculus bactrianus]]''<ref name=Lawal1>{{cite journal |last1=Lawal |first1=R.A. |display-authors=etal |year=2022 |title=Taxonomic assessment of two wild house mouse subspecies using whole-genome sequencing |journal=Scientific Reports |volume=12 |issue=20866 |page=20866 |doi=10.1038/s41598-022-25420-x |doi-access=free |pmid=36460842 |pmc=9718808 |bibcode=2022NatSR..1220866L }}</ref> | ||
*''[[Mus musculus castaneus]]'' | * ''[[Mus musculus castaneus]]'' | ||
*''[[Mus musculus domesticus]]'' | * ''[[Mus musculus domesticus]]'' | ||
*''[[Mus musculus gentilulus]]'' | * ''[[Mus musculus gentilulus]]'' | ||
*''[[Mus musculus molossinus]]'' | * ''[[Mus musculus molossinus]]'' | ||
*†''[[Mus musculus muralis]]'' | * †''[[Mus musculus muralis]]'' | ||
*''[[Mus musculus musculus]]'' | * ''[[Mus musculus musculus]]'' | ||
| range_map = Mapa Mus musculus.png | | range_map = Mapa Mus musculus.png | ||
| range_map_caption = House mouse range (note: distribution is incomplete) | | range_map_caption = House mouse range (note: distribution is incomplete) | ||
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[[File:Mus_musculus_front_teeth.jpg|thumb|left|The house mouse is best identified by the sharp notch in its upper front teeth.]] | [[File:Mus_musculus_front_teeth.jpg|thumb|left|The house mouse is best identified by the sharp notch in its upper front teeth.]] | ||
[[File:Mus musculus MHNT.ZOO.2010.11.236.29.jpg|thumb|left|Skull of ''Mus musculus'' - [[MHNT]]]] | [[File:Mus musculus MHNT.ZOO.2010.11.236.29.jpg|thumb|left|Skull of ''Mus musculus'' - [[MHNT]]]] | ||
House mice have an adult body length (nose to base of tail) of {{convert|7.5|–|10|cm|in|frac=4}} and a tail length of {{convert|5|–|10|cm|in|frac=2|abbr=on}}. The weight is typically {{convert|11|–|30|g|oz|abbr=on|frac=8}}. In the wild they vary in color from grey and light brown to black (individual hairs are actually [[Agouti (coloration)|agouti]] coloured), but domesticated fancy mice and laboratory mice are produced in many colors ranging from white to champagne to pink.<ref name=Berry1970>{{cite journal|author=Berry, R.J.|year=1970|journal=Field Studies|title=The natural history of the house mouse|volume=3|pages=219–62|url=https://www.field-studies-council.org/resources/field-studies-journal/the-natural-history-of-the-house-mouse/|access-date=18 December 2013}}</ref> They have short hair and some, but not all, sub-species have a light belly.<ref name=Berry1970/> The ears and tail have little hair. The hind feet are short compared to ''[[Apodemus]]'' mice, only {{convert|15|–|19|mm|in|frac=16|abbr=on}} long; the normal gait is a run with a stride of about {{convert|4.5|cm|in|frac=4|abbr=on}}, though they can jump vertically up to {{convert|45|cm|in|0|abbr=on}}.<ref>{{cite book|chapter=Rodent-Proof Construction and Exclusion Methods|vauthors=Baker RO, Bodman GR, Timm RM|title=Prevention and Control of Wildlife Damage|year=1994|chapter-url=http://digitalcommons.unl.edu/icwdmhandbook/27/|veditors=Hygnstrom SE, Timm RM, Larson GE|publisher=University of Nebraska-Lincoln}}{{page needed|date=April 2015}}</ref> The voice is a high-pitched squeak.<ref name=lyneborg>{{cite book|author=Lyneborg, L.|year=1971|title=Mammals of Europe|publisher=Blandford Press}}{{page needed|date=April 2015}}</ref><ref name=lawrence>{{cite book|vauthors=Lawrence MJ, Brown RW|year=1974|title=Mammals of Britain Their Tracks, Trails and Signs|publisher=Blandford Press}}{{page needed|date=April 2015}}</ref> House mice thrive under a variety of conditions; they are found in and around homes and commercial structures, as well as in open fields and agricultural lands.<ref>{{Cite web |title=ANRCatalog - House Mouse: Pest Notes for Home and Landscape - ANR Catalog |url=https://anrcatalog.ucanr.edu/Details.aspx?itemNo=7483 |access-date=2025 | House mice have an adult body length (nose to base of tail) of {{convert|7.5|–|10|cm|in|frac=4}} and a tail length of {{convert|5|–|10|cm|in|frac=2|abbr=on}}. The weight is typically {{convert|11|–|30|g|oz|abbr=on|frac=8}}. In the wild they vary in color from grey and light brown to black (individual hairs are actually [[Agouti (coloration)|agouti]] coloured), but domesticated fancy mice and laboratory mice are produced in many colors ranging from white to champagne to pink.<ref name=Berry1970>{{cite journal |author=Berry, R.J. |year=1970 |journal=Field Studies |title=The natural history of the house mouse |volume=3 |pages=219–62 |url=https://www.field-studies-council.org/resources/field-studies-journal/the-natural-history-of-the-house-mouse/ |access-date=18 December 2013 }}</ref> They have short hair and some, but not all, sub-species have a light belly.<ref name=Berry1970/> The ears and tail have little hair. The hind feet are short compared to ''[[Apodemus]]'' mice, only {{convert|15|–|19|mm|in|frac=16|abbr=on}} long; the normal gait is a run with a stride of about {{convert|4.5|cm|in|frac=4|abbr=on}}, though they can jump vertically up to {{convert|45|cm|in|0|abbr=on}}.<ref>{{cite book |chapter=Rodent-Proof Construction and Exclusion Methods |vauthors=Baker RO, Bodman GR, Timm RM |title=Prevention and Control of Wildlife Damage |year=1994 |chapter-url=http://digitalcommons.unl.edu/icwdmhandbook/27/ |veditors=Hygnstrom SE, Timm RM, Larson GE |publisher=University of Nebraska-Lincoln}}{{page needed|date=April 2015 }}</ref> The voice is a high-pitched squeak.<ref name=lyneborg>{{cite book |author=Lyneborg, L. |year=1971 |title=Mammals of Europe |publisher=Blandford Press}}{{page needed|date=April 2015 }}</ref><ref name=lawrence>{{cite book |vauthors=Lawrence MJ, Brown RW |year=1974 |title=Mammals of Britain Their Tracks, Trails and Signs |publisher=Blandford Press}}{{page needed|date=April 2015 }}</ref> House mice thrive under a variety of conditions; they are found in and around homes and commercial structures, as well as in open fields and agricultural lands.<ref>{{Cite web |title=ANRCatalog - House Mouse: Pest Notes for Home and Landscape - ANR Catalog |url=https://anrcatalog.ucanr.edu/Details.aspx?itemNo=7483 |access-date=12 June 2025 |website=anrcatalog.ucanr.edu }}</ref> | ||
Newborn males and females can be distinguished on close examination as the [[anogenital distance]] in males is about double that of the female.<ref>{{cite journal|vauthors=Hotchkiss AK, Vandenbergh JG|title=The anogenital distance index of mice (''Mus musculus domesticus''): an analysis|journal=Contemporary Topics in Laboratory Animal Science|volume=44|issue=4|pages=46–8|date=July 2005|pmid=16050669}}</ref> From the age of about 10 days, females have five pairs of [[mammary gland]]s and [[nipple]]s; males have no nipples.<ref name="Mayer et al">{{cite journal|author-link4=Cheng-Ming Chuong|vauthors=Mayer JA, Foley J, De La Cruz D, Chuong CM, Widelitz R|title=Conversion of the nipple to hair-bearing epithelia by lowering bone morphogenetic protein pathway activity at the dermal-epidermal interface|journal=The American Journal of Pathology|volume=173|issue=5|pages=1339–48|date=November 2008|pmid=18832580|pmc=2570124|doi=10.2353/ajpath.2008.070920}}</ref> When sexually mature, the most striking and obvious difference is the presence of [[testicle]]s on the males. These are large compared to the rest of the body and can be retracted into the body.<ref>{{Citation | | Newborn males and females can be distinguished on close examination as the [[anogenital distance]] in males is about double that of the female.<ref>{{cite journal |vauthors=Hotchkiss AK, Vandenbergh JG |title=The anogenital distance index of mice (''Mus musculus domesticus''): an analysis |journal=Contemporary Topics in Laboratory Animal Science |volume=44 |issue=4 |pages=46–8 |date=July 2005 |pmid=16050669 }}</ref> From the age of about 10 days, females have five pairs of [[mammary gland]]s and [[nipple]]s; males have no nipples.<ref name="Mayer et al">{{cite journal |author-link4=Cheng-Ming Chuong |vauthors=Mayer JA, Foley J, De La Cruz D, Chuong CM, Widelitz R |title=Conversion of the nipple to hair-bearing epithelia by lowering bone morphogenetic protein pathway activity at the dermal-epidermal interface |journal=The American Journal of Pathology |volume=173 |issue=5 |pages=1339–48 |date=November 2008 |pmid=18832580 |pmc=2570124 |doi=10.2353/ajpath.2008.070920 }}</ref> When sexually mature, the most striking and obvious difference is the presence of [[testicle]]s on the males. These are large compared to the rest of the body and can be retracted into the body.<ref>{{Citation |last1=Hickman |first1=D.L. |title=Commonly Used Animal Models |date=2017 |work=Principles of Animal Research |pages=117–175 |publisher=Elsevier |language=en |doi=10.1016/B978-0-12-802151-4.00007-4 |isbn=978-0-12-802151-4 |pmc=7150119 |last2=Johnson |first2=J. |last3=Vemulapalli |first3=T.H. |last4=Crisler |first4=J.R. |last5=Shepherd |first5=R. }}</ref> | ||
The tail, which is used for balance,<ref>{{cite journal|author=Greene, Eunice Chace|year=1935|title=Anatomy of the Rat|journal=Transactions of the American Philosophical Society Held at Philadelphia for Promoting Useful Knowledge|series=Transactions of the American Philosophical Society|volume=27|pages=iii–370|jstor=1005513|oclc=685221899|publisher=American Philosophical Society|doi=10.2307/1005513}}</ref><ref name="Siegel"/><ref>{{cite journal|vauthors=Buck, CW, Tolman N, Tolman, W|date=November 1925|title=The Tail as a Balancing Organ in Mice|journal=Journal of Mammalogy|volume=6|issue=4|pages=267–71|jstor=1373415|doi=10.2307/1373415}}</ref> has only a thin covering of hair as it is the main peripheral organ of heat loss in [[thermoregulation]]<ref name="Siegel">{{cite journal|doi=10.1002/ajpa.1330330113|title=The tail, locomotion and balance in mice|journal=American Journal of Physical Anthropology|volume=33|pages=101–2|year=1970|author=Siegel, Michael I.}}</ref> along with—to a lesser extent—the hairless parts of the paws and ears. Blood flow to the tail can be precisely controlled in response to changes in ambient temperature using a system of [[arteriovenous anastomosis|arteriovenous anastomoses]] to increase the temperature of the skin on the tail by as much as {{convert|10|C-change|K-change F-change}} to lose body heat.<ref name="Nociception">{{cite journal|vauthors=Le Bars D, Gozariu M, Cadden SW|title=Animal models of nociception|journal=Pharmacological Reviews|volume=53|issue=4|pages=597–652|date=December 2001|pmid=11734620}}</ref> Tail length varies according to the environmental temperature of the mouse during postnatal development, so mice living in colder regions tend to have shorter tails.<ref name=Berry1970/> The tail is also used for balance when the mouse is climbing or running, or as a base when the animal stands on its hind legs (a behaviour known as [[Tripod stance|tripoding]]), and to convey information about the dominance status of an individual in encounters with other mice.<ref>{{cite book|author=Drickamer, Lee C.|chapter=Use of the tail for communication in house mice|chapter-url=https://books.google.com/books?id=PQphdAd9KKcC&pg=PA157|pages=157–62|title=Contribuciones mastozoológicas en homenaje a Bernardo Villa|trans-title=Mammal Collection in Honor of Bernardo Villa|language=es|editor1=Víctor, Sánchez-Cordero|editor2=Medellin, Rodrigo A.|publisher=UNAM|isbn=978-970-32-2603-0|year=2005}}</ref> | The tail, which is used for balance,<ref>{{cite journal |author=Greene, Eunice Chace |year=1935 |title=Anatomy of the Rat |journal=Transactions of the American Philosophical Society Held at Philadelphia for Promoting Useful Knowledge |series=Transactions of the American Philosophical Society |volume=27 |pages=iii–370 |jstor=1005513 |oclc=685221899 |publisher=American Philosophical Society |doi=10.2307/1005513 }}</ref><ref name="Siegel"/><ref>{{cite journal |vauthors=Buck, CW, Tolman N, Tolman, W |date=November 1925 |title=The Tail as a Balancing Organ in Mice |journal=Journal of Mammalogy |volume=6 |issue=4 |pages=267–71 |jstor=1373415 |doi=10.2307/1373415 }}</ref> has only a thin covering of hair as it is the main peripheral organ of heat loss in [[thermoregulation]]<ref name="Siegel">{{cite journal |doi=10.1002/ajpa.1330330113 |title=The tail, locomotion and balance in mice |journal=American Journal of Physical Anthropology |volume=33 |pages=101–2 |year=1970 |author=Siegel, Michael I. }}</ref> along with—to a lesser extent—the hairless parts of the paws and ears. Blood flow to the tail can be precisely controlled in response to changes in ambient temperature using a system of [[arteriovenous anastomosis|arteriovenous anastomoses]] to increase the temperature of the skin on the tail by as much as {{convert|10|C-change|K-change F-change}} to lose body heat.<ref name="Nociception">{{cite journal |vauthors=Le Bars D, Gozariu M, Cadden SW |title=Animal models of nociception |journal=Pharmacological Reviews |volume=53 |issue=4 |pages=597–652 |date=December 2001 |doi=10.1016/S0031-6997(24)01514-X |pmid=11734620 }}</ref> Tail length varies according to the environmental temperature of the mouse during postnatal development, so mice living in colder regions tend to have shorter tails.<ref name=Berry1970/> The tail is also used for balance when the mouse is climbing or running, or as a base when the animal stands on its hind legs (a behaviour known as [[Tripod stance|tripoding]]), and to convey information about the dominance status of an individual in encounters with other mice.<ref>{{cite book |author=Drickamer, Lee C. |chapter=Use of the tail for communication in house mice |chapter-url=https://books.google.com/books?id=PQphdAd9KKcC&pg=PA157 |pages=157–62 |title=Contribuciones mastozoológicas en homenaje a Bernardo Villa |trans-title=Mammal Collection in Honor of Bernardo Villa |language=es |editor1=Víctor, Sánchez-Cordero |editor2=Medellin, Rodrigo A. |publisher=UNAM |isbn=978-970-32-2603-0 |year=2005 }}</ref> | ||
In addition to the regular pea-sized [[thymus]] organ in the chest, house mice have a second functional pinhead-sized thymus organ in the neck next to the trachea.<ref name=Terszowski>{{cite journal|vauthors=Terszowski G, Müller SM, Bleul CC, Blum C, Schirmbeck R, Reimann J, Pasquier LD, Amagai T, Boehm T, Rodewald HR|title=Evidence for a functional second thymus in mice|journal=Science|volume=312|issue=5771|pages=284–7|date=April 2006 |pmid=16513945|doi=10.1126/science.1123497|bibcode=2006Sci...312..284T|s2cid=24553384|doi-access=free}}</ref> | In addition to the regular pea-sized [[thymus]] organ in the chest, house mice have a second functional pinhead-sized thymus organ in the neck next to the trachea.<ref name=Terszowski>{{cite journal |vauthors=Terszowski G, Müller SM, Bleul CC, Blum C, Schirmbeck R, Reimann J, Pasquier LD, Amagai T, Boehm T, Rodewald HR |title=Evidence for a functional second thymus in mice |journal=Science |volume=312 |issue=5771 |pages=284–7 |date=April 2006 |pmid=16513945 |doi=10.1126/science.1123497 |bibcode=2006Sci...312..284T |s2cid=24553384 |doi-access=free }}</ref> | ||
==Taxonomy and subspecies== | ==Taxonomy and subspecies== | ||
| Line 42: | Line 43: | ||
| label1=[[Euarchontoglires]] | | label1=[[Euarchontoglires]] | ||
| 1={{Clade | | 1={{Clade | ||
| label1='''Glires''' | |||
| 1={{Clade | |||
| 1=[[Rodent]]ia (rodents) | |||
| 2=[[Lagomorpha]] (rabbits, hares, pikas)}} | |||
| label2=[[Euarchonta]] | |||
| 2={{Clade | |||
| 1=[[Treeshrew|Scandentia]] (treeshrews) | |||
| label2=[[Primatomorpha]] | |||
| 2={{Clade | |||
| 1=[[Colugo|Dermoptera]] (flying lemurs) | |||
| 2={{Clade | |||
| 1=[[Primate]]s (†[[Plesiadapiformes]], [[Strepsirrhini]], [[Haplorrhini]])}}}}}}}} | |||
}} | }} | ||
[[File:Mus musclus molssinus.jpg|thumb|Japanese house mouse | [[File:Mus musclus molssinus.jpg|thumb|Japanese house mouse | ||
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Mice are mammals of the [[Glires]] [[clade]], which means they are amongst the closest relatives of humans other than [[Lagomorpha|lagomorphs]], [[treeshrew]]s, [[flying lemurs]] and other [[primates]]. | Mice are mammals of the [[Glires]] [[clade]], which means they are amongst the closest relatives of humans other than [[Lagomorpha|lagomorphs]], [[treeshrew]]s, [[flying lemurs]] and other [[primates]]. | ||
The three widely accepted [[subspecies]] are increasingly treated as distinct species by some:<ref>{{cite book|author=Mitchell-Jones A.J.|author2=Amori G.|author3=Bogdanowicz W.|author4=Kryštufek B.|author5=Reijnders PJH|author6=Spitzenberger F.|author7=Stubbe M|author8=Thissen JBM|author9=Vohralík V.|author10=Zima J.|year=1999|title=The Atlas of European Mammals|publisher=T. & A. D. Poyser|isbn=978-0-85661-130-8}}{{page needed|date=April 2015}}</ref><ref name=MusserCarleton2005>{{cite book|author=Musser, Guy G.|author2=Carleton, Michael D.|chapter=Superfamily Muroidea|chapter-url=https://books.google.com/books?id=JgAMbNSt8ikC&pg=PA894|editor=Wilson, Don E.|editor2=Reeder, DeeAnn M.|title=Mammal Species of the World: A Taxonomic and Geographic Reference|publisher=Johns Hopkins University Press|location=Baltimore|year=2005|isbn=978-0-8018-8221-0|pages=894–1531|url=http://www.bucknell.edu/msw3|edition=3rd}}</ref> | The three widely accepted [[subspecies]] are increasingly treated as distinct species by some:<ref>{{cite book |author=Mitchell-Jones A.J. |author2=Amori G. |author3=Bogdanowicz W. |author4=Kryštufek B. |author5=Reijnders PJH |author6=Spitzenberger F. |author7=Stubbe M |author8=Thissen JBM |author9=Vohralík V.|author10=Zima J. |year=1999 |title=The Atlas of European Mammals |publisher=T. & A. D. Poyser |isbn=978-0-85661-130-8}}{{page needed|date=April 2015 }}</ref><ref name=MusserCarleton2005>{{cite book |author=Musser, Guy G. |author2=Carleton, Michael D. |chapter=Superfamily Muroidea |chapter-url=https://books.google.com/books?id=JgAMbNSt8ikC&pg=PA894 |editor=Wilson, Don E. |editor2=Reeder, DeeAnn M. |title=Mammal Species of the World: A Taxonomic and Geographic Reference |publisher=Johns Hopkins University Press |location=Baltimore |year=2005 |isbn=978-0-8018-8221-0 |pages=894–1531 |url=http://www.bucknell.edu/msw3 |edition=3rd }}</ref> | ||
*Southeastern Asian house mouse (''Mus musculus castaneus'') (southern and southeastern Asia) | * Southeastern Asian house mouse (''Mus musculus castaneus'') (southern and southeastern Asia) | ||
*Western European house mouse (''[[Mus musculus domesticus]]''); includes the [[fancy mouse]] and the [[laboratory mouse]] (Western Europe, North America, South America, Africa and Oceania) | * Western European house mouse (''[[Mus musculus domesticus]]''); includes the [[fancy mouse]] and the [[laboratory mouse]] (Western Europe, North America, South America, Africa and Oceania) | ||
*Eastern European house mouse (''Mus musculus musculus'') (Eastern Europe and northern Asia) | * Eastern European house mouse (''Mus musculus musculus'') (Eastern Europe and northern Asia) | ||
Two additional subspecies have been recognized more recently:<ref name=MusserCarleton2005/> | Two additional subspecies have been recognized more recently:<ref name=MusserCarleton2005/> | ||
*Southwestern Asian house mouse (''Mus musculus bactrianus'') (southwestern and Central Asia). However, due to significant genetic similarity observed between (''Mus musculus bactrianus'') | * Southwestern Asian house mouse (''Mus musculus bactrianus'') (southwestern and Central Asia). However, due to significant genetic similarity observed between (''Mus musculus bactrianus'') and ''Mus musculus castaneus'', the subspecies designation for ''Mus musculus bactrianus'' has now been questioned.<ref name=Lawal1/> | ||
*pygmy house mouse (''Mus musculus gentilulus'') (the Arabian Peninsula and Madagascar)<ref>{{cite journal|vauthors=Prager EM, Orrego C, Sage RD|title=Genetic variation and phylogeography of central Asian and other house mice, including a major new mitochondrial lineage in Yemen|journal=Genetics|volume=150|issue=2|pages=835–61|date=October 1998|doi=10.1093/genetics/150.2.835|pmid=9755213|pmc=1460354}}</ref> | * pygmy house mouse (''Mus musculus gentilulus'') (the Arabian Peninsula and Madagascar)<ref>{{cite journal |vauthors=Prager EM, Orrego C, Sage RD |title=Genetic variation and phylogeography of central Asian and other house mice, including a major new mitochondrial lineage in Yemen |journal=Genetics |volume=150 |issue=2 |pages=835–61 |date=October 1998 |doi=10.1093/genetics/150.2.835 |pmid=9755213 |pmc=1460354 }}</ref> | ||
Many more subspecies' names have been given to house mice, but these are now regarded as [[Synonym (taxonomy)|synonym]]s of the five subspecies. Some populations are hybrids of different subspecies, including the [[Japanese house mouse]] (''M. m. molossinus'').<ref name=MusserCarleton2005/> A notable region of hybridization is a region in general Europe where ''M. m. domesticus'' and ''M. m. musculus'' are often found to hybridize.<ref>{{cite journal |last1=Turner |first1=Leslie M |last2=Harr |first2=Bettina |title=Genome-wide mapping in a house mouse hybrid zone reveals hybrid sterility loci and Dobzhansky-Muller interactions |journal=eLife |date=9 December 2014 |volume=3 |pages=e02504 |doi=10.7554/eLife.02504.001 |pmid=25487987 |doi-access=free |pmc=4359376 |hdl=11858/00-001M-0000-0024-5B29-0 |hdl-access=free }}</ref> However, male hybrid mice typically experience hybrid sterility, which maintains reproductive separation between the two subspecies.<ref>{{cite journal |last1=Forejt |first1=Jiří |title=Hybrid sterility in the mouse |journal=Trends in Genetics |date=October 1996 |volume=12 |issue=10 |pages=412–417 |doi=10.1016/0168-9525(96)10040-8|pmid=8909138 }}</ref> | Many more subspecies' names have been given to house mice, but these are now regarded as [[Synonym (taxonomy)|synonym]]s of the five subspecies. Some populations are hybrids of different subspecies, including the [[Japanese house mouse]] (''M. m. molossinus'').<ref name=MusserCarleton2005/> A notable region of hybridization is a region in general Europe where ''M. m. domesticus'' and ''M. m. musculus'' are often found to hybridize.<ref>{{cite journal |last1=Turner |first1=Leslie M |last2=Harr |first2=Bettina |title=Genome-wide mapping in a house mouse hybrid zone reveals hybrid sterility loci and Dobzhansky-Muller interactions |journal=eLife |date=9 December 2014 |volume=3 |pages=e02504 |doi=10.7554/eLife.02504.001 |pmid=25487987 |doi-access=free |pmc=4359376 |hdl=11858/00-001M-0000-0024-5B29-0 |hdl-access=free }}</ref> However, male hybrid mice typically experience hybrid sterility, which maintains reproductive separation between the two subspecies.<ref>{{cite journal |last1=Forejt |first1=Jiří |title=Hybrid sterility in the mouse |journal=Trends in Genetics |date=October 1996 |volume=12 |issue=10 |pages=412–417 |doi=10.1016/0168-9525(96)10040-8 |pmid=8909138 }}</ref> | ||
===Chromosomal races=== | ===Chromosomal races=== | ||
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== Evolution == | == Evolution == | ||
Suzuki ''et al.'', 2013 confirms the theory that ''M. musculus'' originates in | Suzuki ''et al.'', 2013 confirms the theory that ''M. musculus'' originates in Southwestern Asia and identifies 5 subspecies and their origins: ''musculus'' in [[northern Eurasia]], ''castaneus'' in India and Southeast Asia, a previously unknown subspecies from [[Nepal]], ''domesticus'' in western Europe, and ''gentilulus'' in [[Yemen]].<ref name="Dispersal"> | ||
{{cite journal|publisher=[[Elsevier BV]]|last1=Chaichan|first1=P.|last2=Mercier|first2=A.|last3=Galal|first3=L.|last4=Mahittikorn|first4=A.|last5=Ariey|first5=F.|last6=Morand|first6=S.|last7=Boumédiène|first7=F.|last8=Udonsom|first8=R.|last9=Hamidovic|first9=A.|last10=Murat|first10=J.B.|last11=Sukthana|first11=Y.|last12=Dardé|first12=M.L.|title=Geographical distribution of ''Toxoplasma gondii'' genotypes in Asia: A link with neighboring continents|journal=[[Infection, Genetics and Evolution]]|volume=53|year=2017|issn=1567-1348|s2cid=4698999|pmid=28583867|doi=10.1016/j.meegid.2017.06.002|pages=227–238|bibcode=2017InfGE..53..227C }} | {{cite journal |publisher=[[Elsevier BV]] |last1=Chaichan |first1=P. |last2=Mercier |first2=A. |last3=Galal |first3=L. |last4=Mahittikorn |first4=A. |last5=Ariey |first5=F. |last6=Morand |first6=S. |last7=Boumédiène |first7=F. |last8=Udonsom |first8=R. |last9=Hamidovic |first9=A.|last10=Murat|first10=J.B. |last11=Sukthana |first11=Y. |last12=Dardé |first12=M.L. |title=Geographical distribution of ''Toxoplasma gondii'' genotypes in Asia: A link with neighboring continents |journal=[[Infection, Genetics and Evolution]] |volume=53 |year=2017 |issn=1567-1348 |s2cid=4698999 |pmid=28583867 |doi=10.1016/j.meegid.2017.06.002 |pages=227–238 |bibcode=2017InfGE..53..227C}} | ||
:This review cites this research. | :This review cites this research. | ||
: | : | ||
:{{cite journal|year=2013|publisher=[[Nature Portfolio]]|last1=Suzuki|first1=H.|last2=Nunome|first2=M.|last3=Kinoshita|first3=G.|last4=Aplin|first4=K. P.|last5=Vogel|first5=P.|last6=Kryukov|first6=A. P.|last7=Jin|first7=M-L|last8=Han|first8=S-H|last9=Maryanto|first9=I.|last10=Tsuchiya|first10=K.|last11=Ikeda|first11=H.|last12=Shiroishi|first12=T.|last13=Yonekawa|first13=H.|last14=Moriwaki|first14=K.|s2cid=25657111|doi=10.1038/hdy.2013.60|title=Evolutionary and dispersal history of Eurasian house mice ''Mus musculus'' clarified by more extensive geographic sampling of mitochondrial DNA|journal=[[Heredity (journal)|Heredity]]|volume=111|issue=5|issn=0018-067X|pages=375–390|pmid=23820581 |id=The [[Genetics Society]]|pmc=3806020}} | :{{cite journal |year=2013 |publisher=[[Nature Portfolio]] |last1=Suzuki |first1=H. |last2=Nunome |first2=M. |last3=Kinoshita |first3=G. |last4=Aplin |first4=K. P. |last5=Vogel |first5=P. |last6=Kryukov |first6=A. P. |last7=Jin |first7=M-L |last8=Han |first8=S-H |last9=Maryanto |first9=I.|last10=Tsuchiya|first10=K. |last11=Ikeda |first11=H. |last12=Shiroishi |first12=T. |last13=Yonekawa |first13=H. |last14=Moriwaki |first14=K. |s2cid=25657111 |doi=10.1038/hdy.2013.60 |title=Evolutionary and dispersal history of Eurasian house mice ''Mus musculus'' clarified by more extensive geographic sampling of mitochondrial DNA |journal=[[Heredity (journal)|Heredity]] |volume=111 |issue=5 |issn=0018-067X |pages=375–390 |pmid=23820581 |id=The [[Genetics Society]] |pmc=3806020 |bibcode=2013Hered.111..375S}} | ||
</ref> | </ref> | ||
A recent study using 89 whole-genome sequences revealed that the modern day ''Mus musculus castaneus'' emerged from an ancestral ''[[Mus musculus]]'' population in Indian subcontinent some time around 700 kya. From there, this ancestral population migrated to Iran around 360 kya to form ''[[Mus musculus domesticus]]'' and then to Afghanistan around 260 kya to form ''Mus musculus musculus''.<ref name=Lawal2>{{cite journal |last1=Lawal |first1=R.A. |last2=Dumont|first2=B.L. |year=2023|title= Ancestral variation and its impact on wild house mouse genomes |journal= bioRxiv |doi= 10.1101/2023.11.09.566486 |doi-access=free }}</ref> | A recent study using 89 whole-genome sequences revealed that the modern day ''Mus musculus castaneus'' emerged from an ancestral ''[[Mus musculus]]'' population in Indian subcontinent some time around 700 kya. From there, this ancestral population migrated to Iran around 360 kya to form ''[[Mus musculus domesticus]]'' and then to Afghanistan around 260 kya to form ''Mus musculus musculus''.<ref name=Lawal2>{{cite journal |last1=Lawal |first1=R.A. |last2=Dumont |first2=B.L. |year=2023 |title=Ancestral variation and its impact on wild house mouse genomes |journal=bioRxiv |doi=10.1101/2023.11.09.566486 |doi-access=free }}</ref> | ||
==Behavior== | ==Behavior== | ||
| Line 89: | Line 90: | ||
Mice are mostly [[Crepuscular animal|crepuscular]] or [[Nocturnality|nocturnal]]; they are averse to bright lights. The average sleep time of a captive house mouse is reported to be 12.5 hours per day.{{citation needed|date=April 2015}} They live in a wide variety of hidden places near food sources, and construct nests from various soft materials. Mice are territorial, and one dominant male usually lives together with several females and young mice. Dominant males respect each other's [[territory (animal)|territories]] and normally enter another's territory only if it is vacant. If two or more males are housed together in a cage, they often become aggressive unless they have been raised together from birth.{{citation needed|date=April 2015}} | Mice are mostly [[Crepuscular animal|crepuscular]] or [[Nocturnality|nocturnal]]; they are averse to bright lights. The average sleep time of a captive house mouse is reported to be 12.5 hours per day.{{citation needed|date=April 2015}} They live in a wide variety of hidden places near food sources, and construct nests from various soft materials. Mice are territorial, and one dominant male usually lives together with several females and young mice. Dominant males respect each other's [[territory (animal)|territories]] and normally enter another's territory only if it is vacant. If two or more males are housed together in a cage, they often become aggressive unless they have been raised together from birth.{{citation needed|date=April 2015}} | ||
House mice primarily feed on plant matter, but are [[Omnivore|omnivorous]].<ref>{{Cite web |last=Kolb |first=Peter |title=Things That Squeak - MSU Extension | House mice primarily feed on plant matter, but are [[Omnivore|omnivorous]].<ref>{{Cite web |last=Kolb |first=Peter |title=Things That Squeak - MSU Extension |publisher=Montana State University |url=https://www.montana.edu/extension/Full_HTML_Pubs/mffn_forestresilienceresistancerestorationandcollaboration/ThingsThatSqueak.html |access-date=12 June 2025 |website=www.montana.edu }}</ref> They [[Coprophagia|eat their own faeces]] to acquire nutrients produced by bacteria in their intestines.<ref>{{cite web |author=Hilscher-Conklin, Caryl |year=1998 |title=Rattus Biologicus: Coprophagy: Healthy Behavior For Your Rats |url=http://www.rmca.org/Articles/coprophagy.htm |work=Rat & Mouse Gazette }}</ref> House mice, like most other rodents, do not vomit.<ref>{{cite journal |vauthors=Horn CC, Kimball BA, Wang H, Kaus J, Dienel S, Nagy A, Gathright GR, Yates BJ, Andrews PL |title=Why can't rodents vomit? A comparative behavioral, anatomical, and physiological study |journal=PLOS ONE |volume=8 |issue=4 |pages=e60537 |year=2013 |pmid=23593236 |pmc=3622671 |doi=10.1371/journal.pone.0060537 |bibcode=2013PLoSO...860537H |doi-access=free}} | ||
*{{cite news |author=Charles Q. Choi |date=April | * {{cite news |author=Charles Q. Choi |date=16 April 2013 |title=Why Woodchucks Don't Upchuck |work=Live Science |url=http://www.livescience.com/28764-rodents-inability-to-vomit.html }}</ref> | ||
Mice are generally afraid of | Mice are generally afraid of rats which often kill and eat them, a behavior known as muricide. Despite this, free-living populations of rats and mice do exist together in forest areas in New Zealand, North America, and elsewhere. House mice are generally poor competitors and in most areas cannot survive away from human settlements in areas where other small mammals, such as [[wood mouse|wood mice]], are present.<ref>{{cite journal |author=Tattersall, Françoise H. |author2=Smith, R. H. |author3=Nowell, F. |year=1997 |title=Experimental colonisation of contrasting habitats by house mice |journal=Zeitschrift für Säugetierkunde |volume=62 |issue=6 |pages=350–8 |url=https://archive.org/stream/zeitschriftfrsu621997deut#page/350/mode/2up }}</ref> However, in some areas (such as Australia), mice are able to coexist with other small rodent species.<ref>{{cite journal |doi=10.1071/WR99016 |title=Movements and refugia of Lakeland Downs short-tailed mice, ''Leggadina lakedownensis'', and house mice, ''Mus domesticus'', on Thevenard Island, Western Australia |journal=Wildlife Research |volume=27 |issue=1 |pages=11–20 |year=2000 |author1=Moro, Dorian |author2=Morris, Keith |bibcode=2000WildR..27...11M }}</ref> | ||
==Social behavior== | ==Social behavior== | ||
The social behavior of the house mouse is not rigidly fixed into species-specific patterns but is instead adaptable to the environmental conditions, such as the availability of food and space.<ref name="Frynta">{{cite journal|doi=10.1002/ab.15555|title=Aggression and commensalism in house mouse: A comparative study across Europe and the near east|journal=Aggressive Behavior|volume=31|issue=3|pages=283–93|year=2005|author1=Frynta, Daniel|author2=Slábová, Markéta|author3=Váchová, Hana|author4=Volfová, Radka|author5=Munclinger, Pavel}}</ref><ref name="Gray">{{cite journal|doi=10.1006/anbe.1996.0301|title=Behavioural mechanisms underlying the spatial dispersion of commensal ''Mus domesticus'' and grassland ''Mus spretus''|journal=Animal Behaviour|volume=53|issue=3|pages=511–24|year=1997|author1=Gray, Samantha J|author2=Hurst, Jane L|s2cid=54989751}}</ref> This adaptability allows house mice to inhabit diverse areas ranging from sandy dunes to apartment buildings.<ref name="Frynta"/> | The social behavior of the house mouse is not rigidly fixed into species-specific patterns but is instead adaptable to the environmental conditions, such as the availability of food and space.<ref name="Frynta">{{cite journal |doi=10.1002/ab.15555 |title=Aggression and commensalism in house mouse: A comparative study across Europe and the near east |journal=Aggressive Behavior |volume=31 |issue=3 |pages=283–93 |year=2005 |author1=Frynta, Daniel |author2=Slábová, Markéta |author3=Váchová, Hana |author4=Volfová, Radka |author5=Munclinger, Pavel }}</ref><ref name="Gray">{{cite journal |doi=10.1006/anbe.1996.0301 |title=Behavioural mechanisms underlying the spatial dispersion of commensal ''Mus domesticus'' and grassland ''Mus spretus'' |journal=Animal Behaviour |volume=53 |issue=3 |pages=511–24 |year=1997 |author1=Gray, Samantha J |author2=Hurst, Jane L |s2cid=54989751 }}</ref> This adaptability allows house mice to inhabit diverse areas ranging from sandy dunes to apartment buildings.<ref name="Frynta"/> | ||
House mice have two forms of social behaviour, the expression of which depends on the environmental context. House mice in buildings and other urbanized areas with close proximity to humans are known as [[commensalism|commensal]].<ref name="Frynta"/> Commensal mice populations often have an excessive food source resulting in high population densities and small home ranges. This causes a switch from territorial behaviour to a hierarchy of individuals.<ref name="Frynta"/><ref>{{cite journal|doi=10.1111/j.1469-7998.1985.tb04914.x|title=Mating behaviour and female choice: Their relation to social structure in wild caught House mice (''Mus musculus'') housed in a semi-natural environment|journal=Journal of Zoology|volume=207|pages=43–51|year=1985|author1=Wolff, Robert J.}}</ref> When populations have an excess of food, there is less female-female aggression, which usually occurs to gain access to food or to prevent infanticide.<ref name="Frynta"/> Male-male aggression occurs in commensal populations, mainly to defend female mates and protect a small territory.<ref name="Frynta"/><ref name="Gray"/> The high level of male-male aggression, with a low female-female aggression level is common in [[Animal sexual behaviour#Polygamy|polygamous]] populations.<ref name="Szenczi">{{cite journal|vauthors=Szenczi P, Bánszegi O, Groó Z, Altbäcker V|title=Development of the social behavior of two mice species with contrasting social systems|journal=Aggressive Behavior|volume=38|issue=4|pages=288–97|year=2012|pmid=25363698|doi=10.1002/ab.21431}}</ref> The social unit of commensal house mouse populations generally consists of one male and two or more females, usually related.<ref name="Szenczi"/><ref name="Dobson">{{cite journal|doi=10.1139/z02-055|title=Experimental tests of spatial association and kinship in monogamous mice (''Mus spicilegus'') and polygynous mice (''Mus musculus domesticus'')|journal=Canadian Journal of Zoology|volume=80|issue=6|pages=980–6|year=2002|author=Dobson, F Stephen|author2=Baudoin, Claude}}</ref> These groups breed cooperatively, with the females communally nursing. This cooperative breeding and rearing by related females helps increase reproductive success. When no related females are present, breeding groups can form from non-related females.<ref name="Dobson"/> | House mice have two forms of social behaviour, the expression of which depends on the environmental context. House mice in buildings and other urbanized areas with close proximity to humans are known as [[commensalism|commensal]].<ref name="Frynta"/> Commensal mice populations often have an excessive food source resulting in high population densities and small home ranges. This causes a switch from territorial behaviour to a hierarchy of individuals.<ref name="Frynta"/><ref>{{cite journal |doi=10.1111/j.1469-7998.1985.tb04914.x |title=Mating behaviour and female choice: Their relation to social structure in wild caught House mice (''Mus musculus'') housed in a semi-natural environment |journal=Journal of Zoology |volume=207 |pages=43–51 |year=1985 |author1=Wolff, Robert J. }}</ref> When populations have an excess of food, there is less female-female aggression, which usually occurs to gain access to food or to prevent infanticide.<ref name="Frynta"/> Male-male aggression occurs in commensal populations, mainly to defend female mates and protect a small territory.<ref name="Frynta"/><ref name="Gray"/> The high level of male-male aggression, with a low female-female aggression level is common in [[Animal sexual behaviour#Polygamy|polygamous]] populations.<ref name="Szenczi">{{cite journal |vauthors=Szenczi P, Bánszegi O, Groó Z, Altbäcker V |title=Development of the social behavior of two mice species with contrasting social systems |journal=Aggressive Behavior |volume=38 |issue=4 |pages=288–97 |year=2012 |pmid=25363698 |doi=10.1002/ab.21431 }}</ref> The social unit of commensal house mouse populations generally consists of one male and two or more females, usually related.<ref name="Szenczi"/><ref name="Dobson">{{cite journal |doi=10.1139/z02-055 |title=Experimental tests of spatial association and kinship in monogamous mice (''Mus spicilegus'') and polygynous mice (''Mus musculus domesticus'') |journal=Canadian Journal of Zoology |volume=80 |issue=6 |pages=980–6 |year=2002 |author=Dobson, F Stephen |author2=Baudoin, Claude |bibcode=2002CaJZ...80..980D }}</ref> These groups breed cooperatively, with the females communally nursing. This cooperative breeding and rearing by related females helps increase reproductive success. When no related females are present, breeding groups can form from non-related females.<ref name="Dobson"/> | ||
In open areas such as shrubs and fields, the house mouse population is known as noncommensal. These populations are often limited by water or food supply and have large territories.<ref name="Gray"/> Female-female aggression in the noncommensal house mouse populations is much higher, reaching a level generally attributed to free-ranging species. Male aggression is also higher in noncommensal populations. In commensal populations, males come into contact with other males quite frequently due to high population densities and aggression must be mediated or the risk of injury becomes too great.<ref name="Frynta"/> | In open areas such as shrubs and fields, the house mouse population is known as noncommensal. These populations are often limited by water or food supply and have large territories.<ref name="Gray"/> Female-female aggression in the noncommensal house mouse populations is much higher, reaching a level generally attributed to free-ranging species. Male aggression is also higher in noncommensal populations. In commensal populations, males come into contact with other males quite frequently due to high population densities and aggression must be mediated or the risk of injury becomes too great.<ref name="Frynta"/> | ||
Both commensal and noncommensal house mouse males aggressively defend their territory and act to exclude all intruders. Males mark their territory by scent marking with urine. In marked territories, intruders showed significantly lower aggression than the territory residents.<ref name="Gray"/> House mice show a male-biased dispersal; males generally leave their birth sites and migrate to form new territories whereas females generally stay and are [[opportunistic breeder]]s rather than seasonal.<ref>{{cite journal|doi=10.1007/s002650050277|jstor=4601248|title=Emigration mechanisms in feral house mice - a laboratory investigation of the influence of social structure, population density, and aggression|journal=Behavioral Ecology and Sociobiology|volume=39|issue=3|pages=159–70|year=1996|author=Gerlach, Gabriele|s2cid=24161932|oclc=299796761}}</ref> | Both commensal and noncommensal house mouse males aggressively defend their territory and act to exclude all intruders. Males mark their territory by scent marking with urine. In marked territories, intruders showed significantly lower aggression than the territory residents.<ref name="Gray"/> House mice show a male-biased dispersal; males generally leave their birth sites and migrate to form new territories whereas females generally stay and are [[opportunistic breeder]]s rather than seasonal.<ref>{{cite journal |doi=10.1007/s002650050277 |jstor=4601248 |title=Emigration mechanisms in feral house mice - a laboratory investigation of the influence of social structure, population density, and aggression |journal=Behavioral Ecology and Sociobiology |volume=39 |issue=3 |pages=159–70 |year=1996 |author=Gerlach, Gabriele |bibcode=1996BEcoS..39..159G |s2cid=24161932 |oclc=299796761 }}</ref> | ||
==Senses and communication== | ==Senses and communication== | ||
| Line 107: | Line 108: | ||
===Vision=== | ===Vision=== | ||
[[File:HouseMouse.jpg|thumb|Adult house mouse]] | [[File:HouseMouse.jpg|thumb|Adult house mouse]] | ||
The visual apparatus of mice is basically similar to that of humans but differs in that they are [[Dichromacy|dichromats]] and have only two types of [[cone cells]] whereas humans are [[Trichromacy|trichromats]] and have three. This means that mice do not perceive some of the colors in the human visual spectrum.<ref name=Smee2007>{{cite journal|doi=10.1038/news070319-12|title=Mice made to see a rainbow of colours|journal=News@nature |year=2007|author=Odling Smee, Lucy|s2cid=211729271|oclc=605144848|doi-access=free}}</ref> However, the [[ventral]] area of the mouse [[retina]] has a much greater density of [[ultraviolet]]-sensitive cones than other areas of the retina, although the biological significance of this structure is unknown.<ref name="Calderone and Jacobs, (1995)">{{cite journal|vauthors=Calderone JB, Jacobs GH|title=Regional variations in the relative sensitivity to UV light in the mouse retina|journal=Visual Neuroscience|volume=12|issue=3|pages=463–8|year=2009|pmid=7654604|doi=10.1017/s0952523800008361|s2cid=45068446 }}</ref><ref name="Yokohyama and Shi, (2000)">{{cite journal|vauthors=Yokoyama S, Shi Y|title=Genetics and evolution of ultraviolet vision in vertebrates|journal=FEBS Letters|volume=486|issue=2|pages=167–72|date=December 2000|pmid=11113460|doi=10.1016/s0014-5793(00)02269-9|s2cid=28891403 |doi-access=|bibcode=2000FEBSL.486..167Y }}</ref><ref name="Neitz and Neitz, (2001)">{{cite journal|vauthors=Neitz M, Neitz J|title=The uncommon retina of the common house mouse|journal=Trends in Neurosciences|volume=24|issue=5|pages=248–50|date=May 2001|pmid=11311361|doi=10.1016/s0166-2236(00)01773-2|s2cid=3756078}}</ref> In 2007, mice genetically engineered to produce the third type of cone were shown to be able to distinguish a range of colors similar to that perceived by [[Tetrachromacy|tetrachromats]].<ref name=Smee2007/> | The visual apparatus of mice is basically similar to that of humans but differs in that they are [[Dichromacy|dichromats]] and have only two types of [[cone cells]] whereas humans are [[Trichromacy|trichromats]] and have three. This means that mice do not perceive some of the colors in the human visual spectrum.<ref name=Smee2007>{{cite journal |doi=10.1038/news070319-12 |title=Mice made to see a rainbow of colours |journal=News@nature |year=2007 |author=Odling Smee, Lucy |s2cid=211729271 |oclc=605144848 |doi-access=free }}</ref> However, the [[ventral]] area of the mouse [[retina]] has a much greater density of [[ultraviolet]]-sensitive cones than other areas of the retina, although the biological significance of this structure is unknown.<ref name="Calderone and Jacobs, (1995)">{{cite journal |vauthors=Calderone JB, Jacobs GH |title=Regional variations in the relative sensitivity to UV light in the mouse retina |journal=Visual Neuroscience |volume=12 |issue=3 |pages=463–8 |year=2009 |pmid=7654604 |doi=10.1017/s0952523800008361 |s2cid=45068446 }}</ref><ref name="Yokohyama and Shi, (2000)">{{cite journal |vauthors=Yokoyama S, Shi Y |title=Genetics and evolution of ultraviolet vision in vertebrates |journal=FEBS Letters |volume=486 |issue=2 |pages=167–72 |date=December 2000 |pmid=11113460 |doi=10.1016/s0014-5793(00)02269-9 |s2cid=28891403 |doi-access= |bibcode=2000FEBSL.486..167Y }}</ref><ref name="Neitz and Neitz, (2001)">{{cite journal |vauthors=Neitz M, Neitz J |title=The uncommon retina of the common house mouse |journal=Trends in Neurosciences |volume=24 |issue=5 |pages=248–50 |date=May 2001 |pmid=11311361 |doi=10.1016/s0166-2236(00)01773-2 |s2cid=3756078 }}</ref> In 2007, mice genetically engineered to produce the third type of cone were shown to be able to distinguish a range of colors similar to that perceived by [[Tetrachromacy|tetrachromats]].<ref name=Smee2007/> | ||
===Olfaction=== | ===Olfaction=== | ||
House mice also rely on [[pheromone]]s for social communication, some of which are produced by the [[preputial gland]]s of both sexes. The tear fluid and urine of male mice also contains pheromones, such as [[major urinary proteins]].<ref>{{cite journal|vauthors=Kimoto H, Haga S, Sato K, Touhara K|title=Sex-specific peptides from exocrine glands stimulate mouse vomeronasal sensory neurons|journal=Nature|volume=437|issue=7060|pages=898–901|date=October 2005|pmid=16208374|doi=10.1038/nature04033|bibcode=2005Natur.437..898K|s2cid=4388164}}</ref><ref>{{cite journal|vauthors=Chamero P, Marton TF, Logan DW, Flanagan K, Cruz JR, Saghatelian A, Cravatt BF, Stowers L|title=Identification of protein pheromones that promote aggressive behaviour|journal=Nature|volume=450|issue=7171|pages=899–902|date=December 2007|pmid=18064011|doi=10.1038/nature05997|bibcode=2007Natur.450..899C|s2cid=4398766}}</ref> Mice detect pheromones mainly with the [[vomeronasal organ]] (Jacobson's organ), located at the bottom of the nose. | House mice also rely on [[pheromone]]s for social communication, some of which are produced by the [[preputial gland]]s of both sexes. The tear fluid and urine of male mice also contains pheromones, such as [[major urinary proteins]].<ref>{{cite journal |vauthors=Kimoto H, Haga S, Sato K, Touhara K |title=Sex-specific peptides from exocrine glands stimulate mouse vomeronasal sensory neurons |journal=Nature |volume=437 |issue=7060 |pages=898–901 |date=October 2005 |pmid=16208374 |doi=10.1038/nature04033 |bibcode=2005Natur.437..898K |s2cid=4388164 }}</ref><ref>{{cite journal |vauthors=Chamero P, Marton TF, Logan DW, Flanagan K, Cruz JR, Saghatelian A, Cravatt BF, Stowers L |title=Identification of protein pheromones that promote aggressive behaviour |journal=Nature |volume=450 |issue=7171 |pages=899–902 |date=December 2007 |pmid=18064011 |doi=10.1038/nature05997 |bibcode=2007Natur.450..899C |s2cid=4398766 }}</ref> Mice detect pheromones mainly with the [[vomeronasal organ]] (Jacobson's organ), located at the bottom of the nose. | ||
The urine of house mice, especially that of males, has a characteristic strong odor. At least 10 different compounds, such as [[alkanes]], [[alcohols]], etc., are detectable in the urine. Among them, five compounds are specific to males, namely 3-cyclohexene-1-methanol, [[aminotriazole]] (3-amino-s-triazole), 4-ethyl phenol, 3-ethyl-2,7-dimethyl octane and 1-iodoundecane.<ref>{{cite journal|vauthors=Achiraman S, Archunan G|title=Characterization of urinary volatiles in Swiss male mice (''Mus musculus''): bioassay of identified compounds|journal=Journal of Biosciences|volume=27|issue=7|pages=679–86|date=December 2002|pmid=12571373|doi=10.1007/BF02708376|s2cid=8533630}}</ref> | The urine of house mice, especially that of males, has a characteristic strong odor. At least 10 different compounds, such as [[alkanes]], [[alcohols]], etc., are detectable in the urine. Among them, five compounds are specific to males, namely 3-cyclohexene-1-methanol, [[aminotriazole]] (3-amino-s-triazole), 4-ethyl phenol, 3-ethyl-2,7-dimethyl octane and 1-iodoundecane.<ref>{{cite journal |vauthors=Achiraman S, Archunan G |title=Characterization of urinary volatiles in Swiss male mice (''Mus musculus''): bioassay of identified compounds |journal=Journal of Biosciences |volume=27 |issue=7 |pages=679–86 |date=December 2002 |pmid=12571373 |doi=10.1007/BF02708376 |s2cid=8533630 }}</ref> | ||
Odours from adult males or from pregnant or lactating females can speed up or retard sexual maturation in juvenile females and synchronise reproductive cycles in mature females (i.e. the [[Whitten effect]]). Odours of unfamiliar male mice may terminate pregnancies, i.e. the [[Bruce effect]]. | Odours from adult males or from pregnant or lactating females can speed up or retard sexual maturation in juvenile females and synchronise reproductive cycles in mature females (i.e. the [[Whitten effect]]). Odours of unfamiliar male mice may terminate pregnancies, i.e. the [[Bruce effect]]. | ||
===Tactile=== | ===Tactile=== | ||
Mice can sense surfaces and air movements with their [[Vibrissae|whiskers]] which are also used during [[thigmotaxis]]. If mice are blind from birth, super-normal growth of the vibrissae occurs presumably as a compensatory response.<ref name="Rauschecker et al., (1992)">{{cite journal|vauthors=Rauschecker JP, Tian B, Korte M, Egert U|title=Crossmodal changes in the somatosensory vibrissa/barrel system of visually deprived animals|journal=Proceedings of the National Academy of Sciences of the United States of America|volume=89|issue=11|pages=5063–7|date=June 1992|pmid= 1594614|pmc=49229|doi=10.1073/pnas.89.11.5063|bibcode=1992PNAS...89.5063R|jstor=2359588|doi-access=free}}</ref> Conversely, if the vibrissae are absent, the use of vision is intensified.<ref name="Sokolov et al., (1986)">{{cite journal|vauthors=Sokolov VE, Tikhonova GN, Tikhonov IA|title=[The role of sensory systems in the behavior of Ryukyu mice (''Mus caroli'' Banhote, 1902)]|language=ru|journal=Izvestiia Akademii Nauk. Seriia Biologicheskaia|issue=2|pages=169–75|year=1996|pmid=8723619}}</ref> | Mice can sense surfaces and air movements with their [[Vibrissae|whiskers]] which are also used during [[thigmotaxis]]. If mice are blind from birth, super-normal growth of the vibrissae occurs presumably as a compensatory response.<ref name="Rauschecker et al., (1992)">{{cite journal |vauthors=Rauschecker JP, Tian B, Korte M, Egert U |title=Crossmodal changes in the somatosensory vibrissa/barrel system of visually deprived animals |journal=Proceedings of the National Academy of Sciences of the United States of America |volume=89 |issue=11 |pages=5063–7 |date=June 1992 |pmid=1594614 |pmc=49229 |doi=10.1073/pnas.89.11.5063 |bibcode=1992PNAS...89.5063R |jstor=2359588 |doi-access=free }}</ref> Conversely, if the vibrissae are absent, the use of vision is intensified.<ref name="Sokolov et al., (1986)">{{cite journal |vauthors=Sokolov VE, Tikhonova GN, Tikhonov IA |title=[The role of sensory systems in the behavior of Ryukyu mice (''Mus caroli'' Banhote, 1902)] |language=ru |journal=Izvestiia Akademii Nauk. Seriia Biologicheskaia |issue=2 |pages=169–75 |year=1996 |pmid=8723619 }}</ref> | ||
==Life cycle and reproduction== | ==Life cycle and reproduction== | ||
| Line 124: | Line 125: | ||
Female house mice have an [[estrus|estrous cycle]] about four to six days long, with estrus itself lasting less than a day. If several females are held together under crowded conditions, they will often not have an estrus at all. If they are then exposed to male urine, they will come into estrus after 72 hours.{{Citation needed|date=June 2024}} | Female house mice have an [[estrus|estrous cycle]] about four to six days long, with estrus itself lasting less than a day. If several females are held together under crowded conditions, they will often not have an estrus at all. If they are then exposed to male urine, they will come into estrus after 72 hours.{{Citation needed|date=June 2024}} | ||
Male house mice court females by emitting characteristic [[ultrasound|ultrasonic]] calls in the 30 kHz–110 kHz {{Citation needed|date=May 2015}} range. The calls are most frequent during courtship when the male is sniffing and following the female; however, the calls continue after mating has begun, at which time the calls are coincident with mounting behaviour. Males can be induced to emit these calls by female pheromones. The vocalizations appear to differ between individuals and have been compared to [[Bird vocalization|bird song]]s because of their complexity.<ref>{{cite journal|vauthors=Holy TE, Guo Z|title=Ultrasonic songs of male mice|journal=PLOS Biology|volume=3|issue=12|pages=e386|date=December 2005|pmid=16248680|pmc=1275525|doi=10.1371/journal.pbio.0030386 |doi-access=free }} | Male house mice court females by emitting characteristic [[ultrasound|ultrasonic]] calls in the 30 kHz–110 kHz {{Citation needed|date=May 2015}} range. The calls are most frequent during courtship when the male is sniffing and following the female; however, the calls continue after mating has begun, at which time the calls are coincident with mounting behaviour. Males can be induced to emit these calls by female pheromones. The vocalizations appear to differ between individuals and have been compared to [[Bird vocalization|bird song]]s because of their complexity.<ref>{{cite journal |vauthors=Holy TE, Guo Z |title=Ultrasonic songs of male mice |journal=PLOS Biology |volume=3 |issue=12 |pages=e386 |date=December 2005 |pmid=16248680 |pmc=1275525 |doi=10.1371/journal.pbio.0030386 |doi-access=free}} | ||
*{{cite web |author=Michael Purdy |date=October | * {{cite web |author=Michael Purdy |date=31 October 2005 |title=Researchers add mice to list of creatures that sing in the presence of mates |website=Washington University in St. Louis |url=http://news.wustl.edu/news/Pages/6040.aspx }}</ref> While females have the capability to produce ultrasonic calls, they typically do not do so during mating behaviour.{{Citation needed|date=June 2024}} | ||
Following copulation, female mice will normally develop a [[mating plug]] which prevents further copulation. The plug is not necessary for pregnancy initiation, as this will also occur without the plug. The presence or absence of the plug will not affect litter size either.<ref name=":1"/> This plug stays in place for some 24 hours. The [[gestation]] period is about 19–21 days, and they give birth to a litter of 3–14 young (average six to eight). One female can have 5 to 10 litters per year, so the mouse population can increase very quickly. Breeding occurs throughout the year. (However, animals living in the wild do not reproduce in the colder months, even though they do not [[Hibernation|hibernate]].){{Citation needed|date=June 2024}} | Following copulation, female mice will normally develop a [[mating plug]] which prevents further copulation. The plug is not necessary for pregnancy initiation, as this will also occur without the plug. The presence or absence of the plug will not affect litter size either.<ref name=":1"/> This plug stays in place for some 24 hours. The [[gestation]] period is about 19–21 days, and they give birth to a litter of 3–14 young (average six to eight). One female can have 5 to 10 litters per year, so the mouse population can increase very quickly. Breeding occurs throughout the year. (However, animals living in the wild do not reproduce in the colder months, even though they do not [[Hibernation|hibernate]].){{Citation needed|date=June 2024}} | ||
The pups are born blind and without fur or ears. The ears are fully developed by the fourth day, fur begins to appear at about six days and the eyes open around 13 days after birth; the pups are weaned at around 21 days. Females reach sexual maturity at about six weeks of age and males at about eight weeks, but both can copulate as early as five weeks.<ref>{{cite web|url=http://www.research.uci.edu/tmf/husbandry.htm#guidelines |archive-url=https://web.archive.org/web/20070704035747/http://www.research.uci.edu/tmf/husbandry.htm#guidelines|archive-date=July | The pups are born blind and without fur or ears. The ears are fully developed by the fourth day, fur begins to appear at about six days and the eyes open around 13 days after birth; the pups are weaned at around 21 days. Females reach sexual maturity at about six weeks of age and males at about eight weeks, but both can copulate as early as five weeks.<ref>{{cite web |url=http://www.research.uci.edu/tmf/husbandry.htm#guidelines |archive-url=https://web.archive.org/web/20070704035747/http://www.research.uci.edu/tmf/husbandry.htm#guidelines |archive-date=4 July 2007 |title=Mouse Husbandry, Breeding and Development |work=University of Carolina, Irvine, Transgenic Mouse Facility Guidelines |publisher=University of Carolina }}</ref> | ||
===Polygamy=== | ===Polygamy=== | ||
Although house mice can be either monogamous or polygamous, they are most commonly [[Animal sexual behaviour#Polygamy|polygamous]]. They generally show characteristics of mate-defense [[Polygyny in animals|polygyny]] in that males are highly territorial and protective of their mates, while females are less [[Agonistic behavior|agonistic]].<ref>{{cite journal|author=Dobson, F Stephen|author2=Jacquot Catherine|title=Experimental tests of spatial association and kinship in monogamous mice and polygynous mice|journal=Canadian Journal of Zoology|date=June 2002|volume=80|issue=6|pages=980–986|doi=10.1139/Z02-055}}</ref> The communal nursing groups that result from these behaviors lead to lower numbers of [[Infanticide in rodents|infanticide]] since more females are able to protect greater numbers of offspring.<ref>{{cite journal|author=Dobson, F Stephen|author2=Jacquot Catherine|author3=Baudoin, Claude|title=An experimental test of kin association in the house mouse|journal=Canadian Journal of Zoology|date=October 2000|volume=78|issue=10|pages=1807–1812|doi=10.1139/z00-100}}</ref> | Although house mice can be either monogamous or polygamous, they are most commonly [[Animal sexual behaviour#Polygamy|polygamous]]. They generally show characteristics of mate-defense [[Polygyny in animals|polygyny]] in that males are highly territorial and protective of their mates, while females are less [[Agonistic behavior|agonistic]].<ref>{{cite journal |author=Dobson, F Stephen |author2=Jacquot Catherine |title=Experimental tests of spatial association and kinship in monogamous mice and polygynous mice |journal=Canadian Journal of Zoology |date=June 2002 |volume=80 |issue=6 |pages=980–986 |doi=10.1139/Z02-055 }}</ref> The communal nursing groups that result from these behaviors lead to lower numbers of [[Infanticide in rodents|infanticide]] since more females are able to protect greater numbers of offspring.<ref>{{cite journal |author=Dobson, F Stephen |author2=Jacquot Catherine |author3=Baudoin, Claude |title=An experimental test of kin association in the house mouse |journal=Canadian Journal of Zoology |date=October 2000 |volume=78 |issue=10 |pages=1807–1812 |doi=10.1139/z00-100 |bibcode=2000CaJZ...78.1806D }}</ref> | ||
====Evolutionary and behavioural consequences==== | ====Evolutionary and behavioural consequences==== | ||
Both evolutionary and behavioral consequences result from the polygamous nature of the house mouse. One consequence is the [[paternal care|paternal investment]], which is lower in polygamous mice than in mice that are monogamous.<ref name=":0"/> This occurs due to the fact that males spend more time involved in [[sexual selection|sexual competition]] than do females, leaving less time for paternal care.<ref name=":0"/> Polygamous male house mice spend less time alone with pups.<ref name=":0"/> They are also less likely and slower to retrieve lost pups than males of monogamous mice.<ref name=":0"/> In contrast, the maternal investment is similar between female mice that have mated once versus multiply.<ref name=":0">{{cite journal|vauthors=Patris B, Baudoin C|title=A comparative study of parental care between two rodent species: implications for the mating system of the mound-building mouse ''Mus spicilegus''|journal=Behavioural Processes|date=October 2000|volume=51|issue=1–3|pages=35–43|doi=10.1016/S0376-6357(00)00117-0|pmid=11074310|s2cid=12674813}}</ref> | Both evolutionary and behavioral consequences result from the polygamous nature of the house mouse. One consequence is the [[paternal care|paternal investment]], which is lower in polygamous mice than in mice that are monogamous.<ref name=":0"/> This occurs due to the fact that males spend more time involved in [[sexual selection|sexual competition]] than do females, leaving less time for paternal care.<ref name=":0"/> Polygamous male house mice spend less time alone with pups.<ref name=":0"/> They are also less likely and slower to retrieve lost pups than males of monogamous mice.<ref name=":0"/> In contrast, the maternal investment is similar between female mice that have mated once versus multiply.<ref name=":0">{{cite journal |vauthors=Patris B, Baudoin C |title=A comparative study of parental care between two rodent species: implications for the mating system of the mound-building mouse ''Mus spicilegus'' |journal=Behavioural Processes |date=October 2000 |volume=51 |issue=1–3 |pages=35–43 |doi=10.1016/S0376-6357(00)00117-0 |pmid=11074310 |s2cid=12674813 }}</ref> | ||
The polygamous behavior of female house mice promotes [[sperm competition]], which affects both male and female [[fitness (biology)|evolutionary fitness]].<ref name=":1"/> Females who mate with multiple males tend to produce both pups in greater numbers,<ref name=":1"/> and with higher survival rates,<ref>{{cite journal|vauthors=Firman RC, Simmons LW|title=Polyandry, sperm competition, and reproductive success in mice|journal=Behavioral Ecology|date=7 March 2008|volume=19|issue=4|pages=695–702|doi=10.1093/beheco/arm158|doi-access=free}}</ref> increasing female fitness. Sperm competition that arises from polygamy favors males with faster, more motile sperm in higher numbers, increasing male fitness.<ref name=":1">{{cite journal|vauthors=Firman RC, Simmons LW|title=Experimental evolution of sperm quality via postcopulatory sexual selection in house mice|journal=Evolution; International Journal of Organic Evolution|volume=64|issue=5|pages=1245–56|date=May 2010|pmid=19922447|doi=10.1111/j.1558-5646.2009.00894.x|doi-access=free}}</ref> The competitive aspect of insemination increases the frequency of polyandrous events and fertilizations. Polyandry has evolved to increase reproductive success.<ref name="Dean, M.D. 2006"/> Male mating behavior is also affected in response to the practice of polygamous behavior. Compared to monogamous house mice, polygamous house mice mate for longer periods of time.<ref name=":2"/> This behaviour allows for an increase in both the transfer of sperm and paternity success, which in turn increases male fitness.<ref name=":2">{{cite journal|author1=Klemme, Ines|author2=Firman, Renée Claire|title=Male house mice that have evolved with sperm competition have increased mating duration and paternity success|journal=Animal Behaviour|date=April 2013|volume=85|issue=4|pages=751–758|doi=10.1016/j.anbehav.2013.01.016|s2cid=17428265}}</ref> | The polygamous behavior of female house mice promotes [[sperm competition]], which affects both male and female [[fitness (biology)|evolutionary fitness]].<ref name=":1"/> Females who mate with multiple males tend to produce both pups in greater numbers,<ref name=":1"/> and with higher survival rates,<ref>{{cite journal |vauthors=Firman RC, Simmons LW |title=Polyandry, sperm competition, and reproductive success in mice |journal=Behavioral Ecology |date=7 March 2008 |volume=19 |issue=4 |pages=695–702 |doi=10.1093/beheco/arm158 |doi-access=free }}</ref> increasing female fitness. Sperm competition that arises from polygamy favors males with faster, more motile sperm in higher numbers, increasing male fitness.<ref name=":1">{{cite journal |vauthors=Firman RC, Simmons LW |title=Experimental evolution of sperm quality via postcopulatory sexual selection in house mice |journal=Evolution; International Journal of Organic Evolution |volume=64 |issue=5 |pages=1245–56 |date=May 2010 |pmid=19922447 |doi=10.1111/j.1558-5646.2009.00894.x |doi-access=free }}</ref> The competitive aspect of insemination increases the frequency of polyandrous events and fertilizations. Polyandry has evolved to increase reproductive success.<ref name="Dean, M.D. 2006"/> Male mating behavior is also affected in response to the practice of polygamous behavior. Compared to monogamous house mice, polygamous house mice mate for longer periods of time.<ref name=":2"/> This behaviour allows for an increase in both the transfer of sperm and paternity success, which in turn increases male fitness.<ref name=":2">{{cite journal |author1=Klemme, Ines |author2=Firman, Renée Claire |title=Male house mice that have evolved with sperm competition have increased mating duration and paternity success |journal=Animal Behaviour |date=April 2013 |volume=85 |issue=4 |pages=751–758 |doi=10.1016/j.anbehav.2013.01.016 |s2cid=17428265 }}</ref> | ||
===Polyandry=== | ===Polyandry=== | ||
As opposed to polygyny, polyandrous behavior in females is the act of breeding with several males in the same season.<ref name=":3">{{cite journal|vauthors=Thonhauser KE, Thoß M, Musolf K, Klaus T, Penn DJ|title=Multiple paternity in wild house mice (''Mus musculus musculus''): effects on offspring genetic diversity and body mass|journal=Ecology and Evolution|volume=4|issue=2|pages=200–9|date=January 2014|pmid=24558575|doi=10.1002/ece3.920|pmc=3925383|bibcode=2014EcoEv...4..200T }}</ref> Variation in number of males that females mate with occurs among a population. Polyandrous behavior is a common mating pattern in the subspecies ''Mus musculus musculus'' as well as its relative ''Mus musculus domesticus''.<ref name=":3"/> | As opposed to polygyny, polyandrous behavior in females is the act of breeding with several males in the same season.<ref name=":3">{{cite journal |vauthors=Thonhauser KE, Thoß M, Musolf K, Klaus T, Penn DJ |title=Multiple paternity in wild house mice (''Mus musculus musculus''): effects on offspring genetic diversity and body mass |journal=Ecology and Evolution |volume=4 |issue=2 |pages=200–9 |date=January 2014 |pmid=24558575 |doi=10.1002/ece3.920 |pmc=3925383 |bibcode=2014EcoEv...4..200T }}</ref> Variation in number of males that females mate with occurs among a population. Polyandrous behavior is a common mating pattern in the subspecies ''Mus musculus musculus'' as well as its relative ''Mus musculus domesticus''.<ref name=":3"/> | ||
[[Polyandry in nature|Polyandry]] occurs in 30% of all wild populations of house mice.<ref name=":4"/> Litters from multiple sires tend to be more genetically diverse than litters of single sires.<ref name=":3"/> Multiple paternity is also more common in larger populations than smaller populations, because there is a larger number of mates and more diverse mates to choose from.<ref name=":4">{{cite journal|vauthors=Firman RC, Simmons LW|title=Polyandry facilitates postcopulatory inbreeding avoidance in house mice|journal=Evolution; International Journal of Organic Evolution|volume=62|issue=3|pages=603–11|date=March 2008|editor=Snook, R.|pmid=18081715|doi=10.1111/j.1558-5646.2007.00307.x|s2cid=23933418|doi-access=free}}</ref> Within a population, males and females show different levels of multiple mating. Females show bias toward unrelated males rather than related males during sexual selection, resulting in more genetically diverse offspring and a reduction of inbreeding depression.<ref name="Dean, M.D. 2006">{{cite journal|author1=Dean, M.D.|author2=Ardlie, K.G.|author3=Nachman, M.W.|year=2006|title=The frequency of multiple paternity suggests that sperm competition is common in house mice (''Mus domesticus'')|journal=Molecular Ecology|volume=15|issue=13|pages=4141–4151|doi=10.1111/j.1365-294x.2006.03068.x|pmid=17054508|pmc=2904556|bibcode=2006MolEc..15.4141D }}</ref> [[Inbreeding depression]] increases genetic incompatibilities, levels of homozygosity, and the chance of expression of deleterious recessive alleles.<ref name="Dean, M.D. 2006"/> Polyandry has been shown to increase offspring survival compared to monandry. | [[Polyandry in nature|Polyandry]] occurs in 30% of all wild populations of house mice.<ref name=":4"/> Litters from multiple sires tend to be more genetically diverse than litters of single sires.<ref name=":3"/> Multiple paternity is also more common in larger populations than smaller populations, because there is a larger number of mates and more diverse mates to choose from.<ref name=":4">{{cite journal |vauthors=Firman RC, Simmons LW |title=Polyandry facilitates postcopulatory inbreeding avoidance in house mice |journal=Evolution; International Journal of Organic Evolution |volume=62 |issue=3 |pages=603–11 |date=March 2008 |editor=Snook, R. |pmid=18081715 |doi=10.1111/j.1558-5646.2007.00307.x |s2cid=23933418 |doi-access=free }}</ref> Within a population, males and females show different levels of multiple mating. Females show bias toward unrelated males rather than related males during sexual selection, resulting in more genetically diverse offspring and a reduction of inbreeding depression.<ref name="Dean, M.D. 2006">{{cite journal |author1=Dean, M.D. |author2=Ardlie, K.G. |author3=Nachman, M.W. |year=2006 |title=The frequency of multiple paternity suggests that sperm competition is common in house mice (''Mus domesticus'') |journal=Molecular Ecology |volume=15 |issue=13 |pages=4141–4151 |doi=10.1111/j.1365-294x.2006.03068.x |pmid=17054508 |pmc=2904556 |bibcode=2006MolEc..15.4141D }}</ref> [[Inbreeding depression]] increases genetic incompatibilities, levels of homozygosity, and the chance of expression of deleterious recessive alleles.<ref name="Dean, M.D. 2006"/> Polyandry has been shown to increase offspring survival compared to monandry. | ||
====Evolutionary consequences==== | ====Evolutionary consequences==== | ||
The fitness of females increases in polyandrous lines due to more genetic diversity and greater litter size.<ref name=":1"/> | The fitness of females increases in polyandrous lines due to more genetic diversity and greater litter size.<ref name=":1"/> | ||
Due to polyandry, males can be confused by the identity of new offspring.<ref name=":5"/> Multiple mating by females and paternity confusion can decrease rates of infanticide.<ref name=":5"/> If the males are uncertain if the offspring are theirs, they are less likely to kill the offspring.<ref name=":5">{{cite journal|vauthors=Auclair Y, König B, Lindholm AK|title=Socially mediated polyandry: a new benefit of communal nesting in mammals|journal=Behavioral Ecology|volume=25|issue=6|pages=1467–1473|date=November 2014|pmid=25419087|doi=10.1093/beheco/aru143|pmc=4235584}}</ref> | Due to polyandry, males can be confused by the identity of new offspring.<ref name=":5"/> Multiple mating by females and paternity confusion can decrease rates of infanticide.<ref name=":5"/> If the males are uncertain if the offspring are theirs, they are less likely to kill the offspring.<ref name=":5">{{cite journal |vauthors=Auclair Y, König B, Lindholm AK |title=Socially mediated polyandry: a new benefit of communal nesting in mammals |journal=Behavioral Ecology |volume=25 |issue=6 |pages=1467–1473 |date=November 2014 |pmid=25419087 |doi=10.1093/beheco/aru143 |pmc=4235584 }}</ref> | ||
Intrauterine insemination causes an evolutionary consequence resulting from polyandrous behavior.<ref name=":6"/> When multiple males mate with one female, there are multiple sets of sperm [[gamete]]s in a female mouse. Offspring fertilized by multiple males can compete more strongly for mother's resources and can lead to a decrease in body size and variation in body size.<ref name=":6">{{cite journal|author1=Firman, R.|author2=Simmons, L.|year=2007|title=Polyandry, sperm competition, and reproductive success in mice|journal=Behavioral Ecology|volume=19|issue=4|pages=695–702|doi=10.1093/beheco/arm158|doi-access=free}}</ref> | Intrauterine insemination causes an evolutionary consequence resulting from polyandrous behavior.<ref name=":6"/> When multiple males mate with one female, there are multiple sets of sperm [[gamete]]s in a female mouse. Offspring fertilized by multiple males can compete more strongly for mother's resources and can lead to a decrease in body size and variation in body size.<ref name=":6">{{cite journal |author1=Firman, R. |author2=Simmons, L. |year=2007 |title=Polyandry, sperm competition, and reproductive success in mice |journal=Behavioral Ecology |volume=19 |issue=4 |pages=695–702 |doi=10.1093/beheco/arm158 |doi-access=free }}</ref> | ||
===Inbreeding avoidance=== | ===Inbreeding avoidance=== | ||
Since [[Inbreeding depression|inbreeding]] is detrimental, it tends to be avoided. In the house mouse, the major urinary protein ([[Major urinary proteins|MUP]]) gene cluster provides a highly polymorphic scent signal of genetic identity that appears to underlie [[kin recognition]] and inbreeding avoidance. Thus there are fewer matings between mice sharing MUP haplotypes than would be expected if there were random mating.<ref name="pmid17997307">{{cite journal|vauthors=Sherborne AL, Thom MD, Paterson S, Jury F, Ollier WE, Stockley P, Beynon RJ, Hurst JL|title=The genetic basis of inbreeding avoidance in house mice|journal=Current Biology|volume=17|issue=23|pages=2061–6|date=December 2007|pmid=17997307|pmc=2148465|doi=10.1016/j.cub.2007.10.041|bibcode=2007CBio...17.2061S }}</ref> Another mechanism for avoiding inbreeding is evident when a female house mouse mates with multiple males. In such a case, there appears to be egg-driven sperm selection against sperm from related males.<ref name="pmid26154782">{{cite journal|vauthors=Firman RC, Simmons LW|title=Gametic interactions promote inbreeding avoidance in house mice|journal=Ecology Letters|volume=18|issue=9|pages=937–43|date=September 2015|pmid=26154782|doi=10.1111/ele.12471|bibcode=2015EcolL..18..937F }}</ref> | Since [[Inbreeding depression|inbreeding]] is detrimental, it tends to be avoided. In the house mouse, the major urinary protein ([[Major urinary proteins|MUP]]) gene cluster provides a highly polymorphic scent signal of genetic identity that appears to underlie [[kin recognition]] and inbreeding avoidance. Thus there are fewer matings between mice sharing MUP haplotypes than would be expected if there were random mating.<ref name="pmid17997307">{{cite journal |vauthors=Sherborne AL, Thom MD, Paterson S, Jury F, Ollier WE, Stockley P, Beynon RJ, Hurst JL |title=The genetic basis of inbreeding avoidance in house mice |journal=Current Biology |volume=17 |issue=23 |pages=2061–6 |date=December 2007 |pmid=17997307 |pmc=2148465 |doi=10.1016/j.cub.2007.10.041 |bibcode=2007CBio...17.2061S }}</ref> Another mechanism for avoiding inbreeding is evident when a female house mouse mates with multiple males. In such a case, there appears to be egg-driven sperm selection against sperm from related males.<ref name="pmid26154782">{{cite journal |vauthors=Firman RC, Simmons LW |title=Gametic interactions promote inbreeding avoidance in house mice |journal=Ecology Letters |volume=18 |issue=9 |pages=937–43 |date=September 2015 |pmid=26154782 |doi=10.1111/ele.12471 |bibcode=2015EcolL..18..937F }}</ref> | ||
==Genetics== | ==Genetics== | ||
As a model organism, a great deal is known about mouse genetics, with a major tool being the [[knockout mouse]] technique. | |||
==Life expectancy== | ==Life expectancy== | ||
[[File:Large Ragdoll cat tosses a mouse.jpg|thumb|right|In both agricultural and urban environments house mice are often preyed upon by the [[Cat|domestic cat]], as with this [[Ragdoll cat|ragdoll]], seen here playing with a mouse it has caught.]] | [[File:Large Ragdoll cat tosses a mouse.jpg|thumb|right|In both agricultural and urban environments house mice are often preyed upon by the [[Cat|domestic cat]], as with this [[Ragdoll cat|ragdoll]], seen here playing with a mouse it has caught.]] | ||
House mice usually live less than one year in the wild, due to a high level of [[predation]] and exposure to harsh environments.<ref>{{Cite journal | | House mice usually live less than one year in the wild, due to a high level of [[predation]] and exposure to harsh environments.<ref>{{Cite journal |last1=Phipatanakul |first1=Wanda |last2=Matsui |first2=Elizabeth |last3=Portnoy |first3=Jay |last4=Williams |first4=P. Brock |last5=Barnes |first5=Charles |last6=Kennedy |first6=Kevin |last7=Bernstein |first7=David |last8=Blessing-Moore |first8=Joann |last9=Cox |first9=Linda |last10=Khan |first10=David |last11=Lang |first11=David |last12=Nicklas |first12=Richard |last13=Oppenheimer |first13=John |last14=Randolph |first14=Christopher |last15=Schuller |first15=Diane |date=December 2012 |title=Environmental assessment and exposure reduction of rodents: a practice parameter |journal=Annals of Allergy, Asthma & Immunology |volume=109 |issue=6 |pages=375–387 |doi=10.1016/j.anai.2012.09.019 |issn=1534-4436 |pmc=3519934 |pmid=23176873 }}</ref> In protected environments, however, they often live two to three years. The [[Methuselah Mouse Prize]] is a competition to breed or engineer extremely long-lived laboratory mice. {{As of|2005}}, the record holder was a genetically engineered mouse that lived for 1,819 days (7 days short of 5 years).<ref>{{cite web |title=Latest Mprize Winners |author=Gobel, D. |work=Andrzej Bartke Mprize for Longevity |orig-date=2003 |year=2013 |url=https://www.sens.org/outreach/conferences/methuselah-mouse-prize |publisher=Methuselah Foundation |access-date=6 February 2019 }}</ref> Another record holder that was kept in an enriched environment but did not receive any genetic, pharmacological, or dietary treatment lived for 1,551 days ({{years and days|1551}}).<ref name=Connor2004>{{cite news |author=Connor, Steve |title=Oldest mouse in captivity wins top science award |url=https://www.questia.com/read/1P2-1885826/oldest-mouse-in-captivity-wins-top-science-award |access-date=30 July 2013 |newspaper=[[The Independent]] (UK) |date=31 October 2004 }}</ref><ref>{{cite web |title=Reversal Prize |publisher=Methuselah Foundation |url=http://www.mfoundation.org/index.php?pagename=reversal |access-date=14 March 2009 |archive-date=30 August 2008 |archive-url=https://web.archive.org/web/20080830080423/http://www.mfoundation.org/index.php?pagename=reversal |url-status=dead }}</ref> | ||
==Aging== | ==Aging== | ||
In several different mouse strains, a significant increase was observed with age in [[8-Oxo-2'-deoxyguanosine]] (8-oxo-dG) levels in nuclear DNA from [[liver]], [[heart]], [[mouse brain|brain]], [[kidney]], [[skeletal muscle]] and [[spleen]].<ref name="Hamilton2001">{{cite journal |vauthors=Hamilton ML, Van Remmen H, Drake JA, Yang H, Guo ZM, Kewitt K, Walter CA, Richardson A |title=Does oxidative damage to DNA increase with age? |journal=Proc Natl Acad Sci U S A |volume=98 |issue=18 |pages=10469–74 |date=August 2001 |pmid=11517304 |pmc=56984 |doi=10.1073/pnas.171202698 }}</ref> | In several different mouse strains, a significant increase was observed with age in [[8-Oxo-2'-deoxyguanosine]] (8-oxo-dG) levels in nuclear DNA from [[liver]], [[heart]], [[mouse brain|brain]], [[kidney]], [[skeletal muscle]] and [[spleen]].<ref name="Hamilton2001">{{cite journal |vauthors=Hamilton ML, Van Remmen H, Drake JA, Yang H, Guo ZM, Kewitt K, Walter CA, Richardson A |title=Does oxidative damage to DNA increase with age? |journal=Proc Natl Acad Sci U S A |volume=98 |issue=18 |pages=10469–74 |date=August 2001 |pmid=11517304 |pmc=56984 |doi=10.1073/pnas.171202698 |doi-access=free |bibcode=2001PNAS...9810469H }}</ref> This increase in [[DNA damage (naturally occurring)|DNA damage]] was attributed to an age related increase in the sensitivity of these tissues to [[oxidative stress]].<ref name = Hamilton2001/> [[Calorie restriction|Dietary restriction]] is known to increase the lifespan of rodents and to retard [[ageing|aging]]. Dietary restriction was found to significantly reduce the age-related accumulation of 8-oxo-dG levels in [[nuclear DNA]] of all tissues studied in mice.<ref name = Hamilton2001/> Thus it was suggested that oxidative DNA damages that arise from normal cellular metabolism could be highly relevant to aging and the diseases of aging.<ref name = Hamilton2001/> In another study, two types of DNA damage (8-hydroxy-2’-deoxyguanosine and DNA-protein crosslinks) were found to increase with age in mouse brain and liver.<ref>{{cite journal |vauthors=Izzotti A, Cartiglia C, Taningher M, De Flora S, Balansky R |title=Age-related increases of 8-hydroxy-2'-deoxyguanosine and DNA-protein crosslinks in mouse organs |journal=Mutat Res |volume=446 |issue=2 |pages=215–23 |date=December 1999 |pmid=10635344 |doi=10.1016/s1383-5718(99)00189-8 |bibcode=1999MRGTE.446..215I }}</ref> | ||
==Mice and humans== | ==Mice and humans== | ||
===History=== | ===History=== | ||
House mice usually live in proximity to humans, in or around houses and/or fields. They are native to [[Animal welfare and rights in India|India]],<ref>{{cite book|title=Museum Notes, Volume 36, Issue 1 – Volume 46, Issue 33|quote=The house mouse originally came from India|publisher=University of Nebraska}}</ref><ref>{{cite journal|doi=10.1046/j.1420-9101.1996.9040391.x|title=Origin and radiation of the house mouse: Mitochondrial DNA phylogeny|journal=Journal of Evolutionary Biology|volume=9|issue=4|pages=391–415|year=1996|vauthors=Boursot P, Din W, Anand R, Darviche D, Dod B, von Deimling F, Talwar GP, Bonhomme F|s2cid=84895257 |doi-access=}}</ref> and later they spread to the eastern Mediterranean about 13,000 BC, only spreading into the rest of Europe around 1000 BC.<ref name=Cucci_etal_2005>{{cite journal|doi=10.1111/j.1095-8312.2005.00445.x|doi-access=free|title=First occurrence of the house mouse (''Mus musculus domesticus'' Schwarz & Schwarz, 1943) in the Western Mediterranean: A zooarchaeological revision of subfossil occurrences|journal=Biological Journal of the Linnean Society|volume=84|issue=3|pages=429–45|year=2005|vauthors=Cucchi T, Vigne JD, Auffray JC|url=https://hal.science/hal-03992863/file/Cucchi_BJLS_2005.pdf}}</ref> This time lag is thought to be because the mice require agrarian human settlements above a certain size.<ref name=Cucci_etal_2005/> The house mouse first arrived in the Americas in the early sixteenth century. It was carried aboard on the ships of Spanish explorers and [[Conquistadors]]. About one hundred years later, it arrived in North America with French fur traders and English colonists. They have since been spread to all parts of the globe by humans.<ref>{{Cite journal |last=Skotnes-Brown |first=Jules |date=March 2023 |title=Scurrying seafarers: shipboard rats, plague, and the land/sea border |url=https://www.cambridge.org/core/journals/journal-of-global-history/article/scurrying-seafarers-shipboard-rats-plague-and-the-landsea-border/36B78B017CD2D36C28F88964DBE30021 |journal=Journal of Global History |language=en |volume=18 |issue=1 |pages=108–130 |doi=10.1017/S1740022822000158 |issn=1740-0228}}</ref> | House mice usually live in proximity to humans, in or around houses and/or fields. They are native to [[Animal welfare and rights in India|India]],<ref>{{cite book |title=Museum Notes, Volume 36, Issue 1 – Volume 46, Issue 33 |quote=The house mouse originally came from India |publisher=University of Nebraska }}</ref><ref>{{cite journal |doi=10.1046/j.1420-9101.1996.9040391.x |title=Origin and radiation of the house mouse: Mitochondrial DNA phylogeny |journal=Journal of Evolutionary Biology |volume=9 |issue=4 |pages=391–415 |year=1996 |vauthors=Boursot P, Din W, Anand R, Darviche D, Dod B, von Deimling F, Talwar GP, Bonhomme F |s2cid=84895257 |doi-access= }}</ref> and later they spread to the eastern Mediterranean about 13,000 BC, only spreading into the rest of Europe around 1000 BC.<ref name=Cucci_etal_2005>{{cite journal |doi=10.1111/j.1095-8312.2005.00445.x |doi-access=free |title=First occurrence of the house mouse (''Mus musculus domesticus'' Schwarz & Schwarz, 1943) in the Western Mediterranean: A zooarchaeological revision of subfossil occurrences |journal=Biological Journal of the Linnean Society |volume=84 |issue=3 |pages=429–45 |year=2005 |vauthors=Cucchi T, Vigne JD, Auffray JC |url=https://hal.science/hal-03992863/file/Cucchi_BJLS_2005.pdf }}</ref> This time lag is thought to be because the mice require agrarian human settlements above a certain size.<ref name=Cucci_etal_2005/> The house mouse first arrived in the Americas in the early sixteenth century. It was carried aboard on the ships of Spanish explorers and [[Conquistadors]]. About one hundred years later, it arrived in North America with French fur traders and English colonists. They have since been spread to all parts of the globe by humans.<ref>{{Cite journal |last=Skotnes-Brown |first=Jules |date=March 2023 |title=Scurrying seafarers: shipboard rats, plague, and the land/sea border |url=https://www.cambridge.org/core/journals/journal-of-global-history/article/scurrying-seafarers-shipboard-rats-plague-and-the-landsea-border/36B78B017CD2D36C28F88964DBE30021 |journal=Journal of Global History |language=en |volume=18 |issue=1 |pages=108–130 |doi=10.1017/S1740022822000158 |issn=1740-0228 |hdl=10023/25280 |hdl-access=free }}</ref> | ||
Many studies have been done on mouse phylogenies to reconstruct early human movements. For example, one study suggests the possibility of a previously unsuspected early link between Northern Europe and Madeira on the basis of the origin of Madeiran mice.<ref>{{cite journal|vauthors=Gündüz I, Auffray JC, Britton-Davidian J, Catalan J, Ganem G, Ramalhinho MG, Mathias ML, Searle JB|title=Molecular studies on the colonization of the Madeiran archipelago by house mice|journal=Molecular Ecology|volume=10|issue=8|pages=2023–9|date=August 2001|pmid=11555245|doi=10.1046/j.0962-1083.2001.01346.x|bibcode=2001MolEc..10.2023G |s2cid=19068030}}</ref> House mice were thought to be the primary reason for the [[Evolution of the domesticated cat|domestication of cats]].<ref>{{Cite web |last=O'Brien |first=Carlos A. Driscoll, Juliet Clutton-Brock, Andrew C. Kitchener, Stephen J. |date=2009 | Many studies have been done on mouse phylogenies to reconstruct early human movements. For example, one study suggests the possibility of a previously unsuspected early link between Northern Europe and Madeira on the basis of the origin of Madeiran mice.<ref>{{cite journal |vauthors=Gündüz I, Auffray JC, Britton-Davidian J, Catalan J, Ganem G, Ramalhinho MG, Mathias ML, Searle JB |title=Molecular studies on the colonization of the Madeiran archipelago by house mice |journal=Molecular Ecology |volume=10 |issue=8 |pages=2023–9 |date=August 2001 |pmid=11555245 |doi=10.1046/j.0962-1083.2001.01346.x |bibcode=2001MolEc..10.2023G |s2cid=19068030 }}</ref> House mice were thought to be the primary reason for the [[Evolution of the domesticated cat|domestication of cats]].<ref>{{Cite web |last=O'Brien |first=Carlos A. Driscoll, Juliet Clutton-Brock, Andrew C. Kitchener, Stephen J. |date=1 June 2009 |title=The Evolution of House Cats |url=https://www.scientificamerican.com/article/the-taming-of-the-cat/ |access-date=12 June 2025 |website=Scientific American |language=en }}</ref> | ||
===As pets=== | ===As pets=== | ||
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[[File:Petmouse.JPG|thumb|left|Fancy mice may be of colours and/or have markings not found in wild mice.]] | [[File:Petmouse.JPG|thumb|left|Fancy mice may be of colours and/or have markings not found in wild mice.]] | ||
The first written reference to mice kept as pets occurs in the ''[[Erya]]'', the oldest extant Chinese dictionary, from a mention in an 1100 BC version.<ref>{{cite web|title=The History Of Fancy Mice|url=http://www.afrma.org/rminfo4b.htm|publisher=American Fancy Rat and Mouse Association|access-date=29 July 2013|archive-url=https://web.archive.org/web/20091005015417/http://www.afrma.org/rminfo4b.htm|archive-date=5 October 2009|url-status=dead}}</ref> Human domestication led to numerous strains of "[[Animal fancy|fancy]]" or hobby mice with a variety of colours and a docile [[temperament]].<ref name="Mouse Club">[http://www.rmca.org/Resources/mousefaq.htm the Rat and Mouse Club of America]</ref> Domestic varieties of the house mouse are bred as a food source for some [[carnivorous]] pet | The first written reference to mice kept as pets occurs in the ''[[Erya]]'', the oldest extant Chinese dictionary, from a mention in an 1100 BC version.<ref>{{cite web |title=The History Of Fancy Mice |url=http://www.afrma.org/rminfo4b.htm |publisher=American Fancy Rat and Mouse Association |access-date=29 July 2013 |archive-url=https://web.archive.org/web/20091005015417/http://www.afrma.org/rminfo4b.htm |archive-date=5 October 2009 |url-status=dead }}</ref> Human domestication led to numerous strains of "[[Animal fancy|fancy]]" or hobby mice with a variety of colours and a docile [[temperament]].<ref name="Mouse Club">[http://www.rmca.org/Resources/mousefaq.htm the Rat and Mouse Club of America]</ref> Domestic varieties of the house mouse are bred as a food source for some [[carnivorous]] pet reptiles, birds, [[arthropod]]s, and fish.<ref name="Mouse Club"/> The effects of domestication can be rapid, with captive-reared mice differing in boldness and activity patterns compared to wild-caught mice after 4–5 generations in recent research.<ref name="Jones1">{{cite journal |author=Courtney Jones, Stephanie K. |author2=Byrne, Phillip G. |title=What role does heritability play in transgenerational phenotypic responses to captivity? Implications for managing captive populations |journal=Zoo Biology |date=December 2017 |volume=36 |issue=6 |pages=397–406 |doi=10.1002/zoo.21389 |pmid=29193268 }}</ref><ref name="Jones 2">{{cite journal |author=Courtney Jones, Stephanie K. |author2=Munn, Adam J. |author3=Byrne, Phillip G. |title=Effects of captivity on house mice behaviour in a novel environment: Implications for conservation practices |journal=Applied Animal Behaviour Science |date=April 2017 |volume=189 |pages=98–106 |doi=10.1016/j.applanim.2017.01.007 |url=http://ro.uow.edu.au/cgi/viewcontent.cgi?article=5546&context=smhpapers }}</ref> | ||
===Mice as pests=== | ===Mice as pests=== | ||
[[File:Mus musculus 01.JPG|thumb|Infestation of mice. Taxidermy display, [[Staatliches Museum für Naturkunde Karlsruhe]], Germany.]] | [[File:Mus musculus 01.JPG|thumb|Infestation of mice. Taxidermy display, [[Staatliches Museum für Naturkunde Karlsruhe]], Germany.]] | ||
Mice are widespread [[Pest (organism)|pest]] organisms, and one of the most common rodents to infest human buildings. They commonly forage outdoors during the spring and summer, but retreat into buildings through the autumn and winter to seek warmth and food. They typically feed on unattended food, leftovers and garden produce. Their foraging risks the contamination and degradation of food supplies, and can also spread other pests such as [[flea]]s, [[tick]]s, [[Louse|lice]] and [[ | Mice are widespread [[Pest (organism)|pest]] organisms, and one of the most common rodents to infest human buildings. They commonly forage outdoors during the spring and summer, but retreat into buildings through the autumn and winter to seek warmth and food. They typically feed on unattended food, leftovers and garden produce. Their foraging risks the contamination and degradation of food supplies, and can also spread other pests such as [[flea]]s, [[tick]]s, [[Louse|lice]] and [[mite]]s.<ref>{{Cite journal |last1=Ho |first1=Jeffery |last2=Changbunjong |first2=Tanasak |last3=Weluwanarak |first3=Thekhawet |last4=Hussain |first4=Sabir |last5=Sparagano |first5=Olivier |date=1 March 2021 |title=The pests of a pest: A systematic review of ectoparasitic fauna among synanthropic rodents in the 21st century with meta-analysis |url=https://www.sciencedirect.com/science/article/pii/S0001706X20317150 |journal=Acta Tropica |volume=215 |pages=105802 |doi=10.1016/j.actatropica.2020.105802 |pmid=33352168 |issn=0001-706X |url-access=subscription }}</ref> | ||
When infesting homes, house mice may pose a risk of damaging and compromising the structure of furniture and the building itself. They gnaw various materials to file down their growing teeth and keep the length under control. Common damage includes gnawed electrical wires, marks on wooden furniture and construction supporting elements, and textile damage.<ref>{{Cite book |url=https://www.nps.gov/orgs/1103/upload/NPS-Rodent-Exclusion-Manual-Mechanical-Rodent-Proofing-Techniques_2019_508.pdf |title=Rodent Exclusion Manual: Mechanical Rodent Proofing Techniques: a training manual for National Park Service Employees |publisher=[[National Park Service]] |via=[[U.S. Department of the Interior]]}}</ref> | When infesting homes, house mice may pose a risk of damaging and compromising the structure of furniture and the building itself. They gnaw various materials to file down their growing teeth and keep the length under control. Common damage includes gnawed electrical wires, marks on wooden furniture and construction supporting elements, and textile damage.<ref>{{Cite book |url=https://www.nps.gov/orgs/1103/upload/NPS-Rodent-Exclusion-Manual-Mechanical-Rodent-Proofing-Techniques_2019_508.pdf |title=Rodent Exclusion Manual: Mechanical Rodent Proofing Techniques: a training manual for National Park Service Employees |publisher=[[National Park Service]] |via=[[U.S. Department of the Interior]] }}</ref> | ||
===Mice and diseases=== | ===Mice and diseases=== | ||
House mice can sometimes transmit diseases, contaminate food, and damage food packaging. Although the [[Centers for Disease Control and Prevention]] provides a list with diseases transmitted by rodents,<ref name="cdc.gov">{{cite web|title=Diseases directly transmitted by rodents|publisher=Centers for Disease Control and Prevention (page last updated: June | House mice can sometimes transmit diseases, contaminate food, and damage food packaging. Although the [[Centers for Disease Control and Prevention]] provides a list with diseases transmitted by rodents,<ref name="cdc.gov">{{cite web |title=Diseases directly transmitted by rodents |publisher=Centers for Disease Control and Prevention (page last updated: 7 June 2011) |url=https://www.cdc.gov/rodents/diseases/direct.html |date=4 September 2018 }}</ref> only a few of the diseases are transmitted through the house mouse.<ref>{{Cite journal |last1=Panti-May |first1=J. A. |last2=DE Andrade |first2=R. R. C. |last3=Gurubel-González |first3=Y. |last4=Palomo-Arjona |first4=E. |last5=Sodá-Tamayo |first5=L. |last6=Meza-Sulú |first6=J. |last7=Ramírez-Sierra |first7=M. |last8=Dumonteil |first8=E. |last9=Vidal-Martínez |first9=V. M. |last10=Machaín-Williams |first10=C. |last11=DE Oliveira |first11=D. |last12=Reis |first12=M. G. |last13=Torres-Castro |first13=M. A. |last14=Robles |first14=M. R. |last15=Hernández-Betancourt |first15=S. F. |date=August 2017 |title=A survey of zoonotic pathogens carried by house mouse and black rat populations in Yucatan, Mexico |journal=Epidemiology and Infection |volume=145 |issue=11 |pages=2287–2295 |doi=10.1017/S0950268817001352 |issn=1469-4409 |pmc=6231242 |pmid=28689507 }}</ref> | ||
[[Lymphocytic choriomeningitis]] (LCMV) can be transmitted by mice, but is not a commonly reported infection in humans, though most infections are mild and are often never diagnosed.<ref>{{cite web|url=http://www.cfsph.iastate.edu/Factsheets/pdfs/lymphocytic_choriomeningitis.pdf|publisher=Iowa State University Center for Food Security and Public Health|date=March 2010|title=Lymphocytic Choriomeningitis}}</ref><ref>{{cite journal|vauthors=Verhaegh EM, Moudrous W, Buiting AG, van der Eijk AA, Tijssen CC|title=[Meningitis after a mouse bite]|language=nl|journal=Nederlands Tijdschrift voor Geneeskunde|volume=158|pages=A7033|year=2014|pmid=25017980|trans-title=Meningitis after a mouse bite}}</ref><ref>{{cite journal|title=Interim guidance for minimizing risk for human lymphocytic choriomeningitis virus infection associated with rodents|journal=MMWR. Morbidity and Mortality Weekly Report|volume=54|issue=30|pages=747–9|date=August 2005|pmid=16079740|author=Centers for Disease Control Prevention (CDC)}}</ref> Some concern exists that women should not be infected with LCMV during pregnancy.<ref>{{cite journal|vauthors=Jamieson DJ, Kourtis AP, Bell M, Rasmussen SA|title=Lymphocytic choriomeningitis virus: an emerging obstetric pathogen?|journal=American Journal of Obstetrics and Gynecology|volume=194|issue=6|pages=1532–6|date=June 2006|pmid=16731068|doi=10.1016/j.ajog.2005.11.040|url=https://zenodo.org/record/1258688}}</ref><ref>{{cite journal|author=Bonthius, DJ|title=Lymphocytic choriomeningitis virus: an underrecognized cause of neurologic disease in the fetus, child, and adult|journal=Seminars in Pediatric Neurology|volume=19|issue=3|pages=89–95|date=September 2012|pmid=22889536|pmc=4256959|doi=10.1016/j.spen.2012.02.002}}</ref> | [[Lymphocytic choriomeningitis]] (LCMV) can be transmitted by mice, but is not a commonly reported infection in humans, though most infections are mild and are often never diagnosed.<ref>{{cite web |url=http://www.cfsph.iastate.edu/Factsheets/pdfs/lymphocytic_choriomeningitis.pdf |publisher=Iowa State University Center for Food Security and Public Health |date=March 2010 |title=Lymphocytic Choriomeningitis }}</ref><ref>{{cite journal |vauthors=Verhaegh EM, Moudrous W, Buiting AG, van der Eijk AA, Tijssen CC |title=[Meningitis after a mouse bite] |language=nl |journal=Nederlands Tijdschrift voor Geneeskunde |volume=158 |pages=A7033 |year=2014 |pmid=25017980 |trans-title=Meningitis after a mouse bite }}</ref><ref>{{cite journal |title=Interim guidance for minimizing risk for human lymphocytic choriomeningitis virus infection associated with rodents |journal=MMWR. Morbidity and Mortality Weekly Report |volume=54 |issue=30 |pages=747–9 |date=August 2005 |pmid=16079740 |author=Centers for Disease Control Prevention (CDC) }}</ref> Some concern exists that women should not be infected with LCMV during pregnancy.<ref>{{cite journal |vauthors=Jamieson DJ, Kourtis AP, Bell M, Rasmussen SA |title=Lymphocytic choriomeningitis virus: an emerging obstetric pathogen? |journal=American Journal of Obstetrics and Gynecology |volume=194 |issue=6 |pages=1532–6 |date=June 2006 |pmid=16731068 |doi=10.1016/j.ajog.2005.11.040 |url=https://zenodo.org/record/1258688 }}</ref><ref>{{cite journal |author=Bonthius, DJ |title=Lymphocytic choriomeningitis virus: an underrecognized cause of neurologic disease in the fetus, child, and adult |journal=Seminars in Pediatric Neurology |volume=19 |issue=3 |pages=89–95 |date=September 2012 |pmid=22889536 |pmc=4256959 |doi=10.1016/j.spen.2012.02.002 }}</ref> | ||
House mice are not usually a vector of human plague ([[bubonic plague]]) because they have fewer infestations with fleas than do rats, and because the fleas which house mice normally carry exhibit little tendency to bite humans rather than their natural host.<ref>{{cite book|title=A History of Bubonic Plague in the British Isles|page=15|author=Shrewsbury, J. F. D.|publisher=Cambridge University Press|year=1970}}</ref> | House mice are not usually a vector of human plague ([[bubonic plague]]) because they have fewer infestations with fleas than do rats, and because the fleas which house mice normally carry exhibit little tendency to bite humans rather than their natural host.<ref>{{cite book |title=A History of Bubonic Plague in the British Isles |page=15 |author=Shrewsbury, J. F. D. |publisher=Cambridge University Press |year=1970 }}</ref> | ||
[[Rickettsialpox]], caused by the bacterium ''[[Rickettsia akari]]'' and similar to [[chickenpox]], is spread by mice in general, but is very rare and generally mild and resolves within two or three weeks if untreated. No known deaths have resulted from the disease. [[Murine typhus]] (also called endemic typhus), caused by the bacterium ''[[Rickettsia typhi]]'', is transmitted by the fleas that infest rats. While rat fleas are the most common vectors, cat fleas and mouse fleas are less common modes of transmission.<ref>"A previous study [1943] reported house mice naturally infected with ''R. typhi'' in the state of Georgia; however, no PCR-positive mice were detected in our study. Eruptions of mouse populations in the absence of rats have been implicated in several outbreaks of murine typhus; however, these observations were not supported by laboratory data." {{cite journal|vauthors=Eremeeva ME, Warashina WR, Sturgeon MM, Buchholz AE, Olmsted GK, Park SY, Effler PV, Karpathy SE|title=Rickettsia typhi and R. felis in rat fleas (Xenopsylla cheopis), Oahu, Hawaii|journal=Emerging Infectious Diseases|volume=14|issue=10|pages=1613–5|date=October 2008|pmid=18826827|pmc=2609893|doi=10.3201/eid1410.080571}}</ref> Endemic typhus is highly treatable with antibiotics. The U.S. CDC currently does not mention rickettsialpox or murine typhus on its website about diseases directly transmitted by rodents (in general).<ref name="cdc.gov"/> | [[Rickettsialpox]], caused by the bacterium ''[[Rickettsia akari]]'' and similar to [[chickenpox]], is spread by mice in general, but is very rare and generally mild and resolves within two or three weeks if untreated. No known deaths have resulted from the disease. [[Murine typhus]] (also called endemic typhus), caused by the bacterium ''[[Rickettsia typhi]]'', is transmitted by the fleas that infest rats. While rat fleas are the most common vectors, cat fleas and mouse fleas are less common modes of transmission.<ref>"A previous study [1943] reported house mice naturally infected with ''R. typhi'' in the state of Georgia; however, no PCR-positive mice were detected in our study. Eruptions of mouse populations in the absence of rats have been implicated in several outbreaks of murine typhus; however, these observations were not supported by laboratory data." {{cite journal |vauthors=Eremeeva ME, Warashina WR, Sturgeon MM, Buchholz AE, Olmsted GK, Park SY, Effler PV, Karpathy SE |title=Rickettsia typhi and R. felis in rat fleas (Xenopsylla cheopis), Oahu, Hawaii |journal=Emerging Infectious Diseases |volume=14 |issue=10 |pages=1613–5 |date=October 2008 |pmid=18826827 |pmc=2609893 |doi=10.3201/eid1410.080571 }}</ref> Endemic typhus is highly treatable with antibiotics. The U.S. CDC currently does not mention rickettsialpox or murine typhus on its website about diseases directly transmitted by rodents (in general).<ref name="cdc.gov"/> | ||
[[Leptospirosis]] is carried by a variety of wild and domestic animals including dogs, rats, swine, cattle, mice in general, and can be transmitted by the urine of an infected animal and is contagious as long as the urine is still moist.<ref>{{cite journal|vauthors=Brown K, Prescott J|title=Leptospirosis in the family dog: a public health perspective|journal=CMAJ|volume=178|issue=4|pages=399–401|date=February 2008|pmid=18268265|pmc=2228361|doi=10.1503/cmaj.071097}}</ref> | [[Leptospirosis]] is carried by a variety of wild and domestic animals including dogs, rats, swine, cattle, mice in general, and can be transmitted by the urine of an infected animal and is contagious as long as the urine is still moist.<ref>{{cite journal |vauthors=Brown K, Prescott J |title=Leptospirosis in the family dog: a public health perspective |journal=CMAJ |volume=178 |issue=4 |pages=399–401 |date=February 2008 |pmid=18268265 |pmc=2228361 |doi=10.1503/cmaj.071097 }}</ref> | ||
In Central Europe, the Dobriva sequence of [[Hantavirus pulmonary syndrome|hantavirus]] has been found in house mice. This is the most serious type of [[Hanta virus|hanta]] that can infect humans.<ref>{{Cite journal|last1=Weidmann|first1=Manfred|last2=Schmidt|first2=P.|last3=Vackova|first3=M.|last4=Krivanec|first4=K.|last5=Munclinger|first5=P.|last6=Hufert|first6=F. T.|date=February 2005|title=Identification of Genetic Evidence for Dobrava Virus Spillover in Rodents by Nested Reverse Transcription (RT)-PCR and TaqMan RT-PCR|journal=Journal of Clinical Microbiology|volume=43|issue=2|pages=808–812|doi=10.1128/JCM.43.2.808-812.2005|pmid=15695684|pmc=548048}}</ref> | In Central Europe, the Dobriva sequence of [[Hantavirus pulmonary syndrome|hantavirus]] has been found in house mice. This is the most serious type of [[Hanta virus|hanta]] that can infect humans.<ref>{{Cite journal |last1=Weidmann |first1=Manfred |last2=Schmidt |first2=P. |last3=Vackova |first3=M. |last4=Krivanec |first4=K. |last5=Munclinger |first5=P. |last6=Hufert |first6=F. T. |date=February 2005 |title=Identification of Genetic Evidence for Dobrava Virus Spillover in Rodents by Nested Reverse Transcription (RT)-PCR and TaqMan RT-PCR |journal=Journal of Clinical Microbiology |volume=43 |issue=2 |pages=808–812 |doi=10.1128/JCM.43.2.808-812.2005 |pmid=15695684 |pmc=548048 }}</ref> | ||
Mice contribute indirectly to the transmission of [[Lyme disease]] by acting as hosts for tick larvae.<ref>{{Cite web |title=The Hidden Complexity of Mice |url=https://abasprixextermination.com/mice-hidden-complexity.html |access-date=2025 | Mice contribute indirectly to the transmission of [[Lyme disease]] by acting as hosts for tick larvae.<ref>{{Cite web |title=The Hidden Complexity of Mice |url=https://abasprixextermination.com/mice-hidden-complexity.html |access-date=12 June 2025 |website=abasprixextermination.com }}</ref> When young ticks feed on infected mice, they acquire the bacteria responsible for the disease. As these ticks mature, they can transmit the infection to humans and other animals through subsequent bites, thereby playing a crucial role in the disease's ecological cycle.<ref>{{Cite web |date=28 August 2023 |title=Wild immunology: Mice, habitat quality and the spread of Lyme disease |url=https://hscweb3.hsc.usf.edu/health/publichealth/news/wild-immunology-mice-habitat-quality-and-the-spread-of-lyme-disease/ |access-date=12 June 2025 |website=College of Public Health News }}</ref> | ||
===Invasive species=== | ===Invasive species=== | ||
Mice have become an [[invasive species]] on islands to where they have spread during the period of European exploration and colonisation.<ref>{{Cite journal | | Mice have become an [[invasive species]] on islands to where they have spread during the period of European exploration and colonisation.<ref>{{Cite journal |last1=Gabriel |first1=S. I. |last2=Mathias |first2=M. L. |last3=Searle |first3=J. B. |date=2015 |title=Of mice and the 'Age of Discovery': the complex history of colonization of the Azorean archipelago by the house mouse (Mus musculus) as revealed by mitochondrial DNA variation |url=https://onlinelibrary.wiley.com/doi/abs/10.1111/jeb.12550 |journal=Journal of Evolutionary Biology |language=en |volume=28 |issue=1 |pages=130–145 |doi=10.1111/jeb.12550 |pmid=25394749 |issn=1420-9101 }}</ref> | ||
New Zealand had no land mammals other than two species of bat prior to human occupation, and the house mouse is one of many species that have been introduced. Mice are responsible for a reduction in native bird species since they eat some of the same foods as birds. They are also known to kill lizards and have a large effect on native insects.<ref>{{cite book |publisher=Oxford University Press|isbn=978-0-19-558320-5|editor=King, Caroline|title=The Handbook of New Zealand Mammals|location=Auckland, N.Z.|year=1995}}{{page needed|date=April 2015}}</ref> | New Zealand had no land mammals other than two species of bat prior to human occupation, and the house mouse is one of many species that have been introduced. Mice are responsible for a reduction in native bird species since they eat some of the same foods as birds. They are also known to kill lizards and have a large effect on native insects.<ref>{{cite book |publisher=Oxford University Press |isbn=978-0-19-558320-5 |editor=King, Caroline |title=The Handbook of New Zealand Mammals |location=Auckland, N.Z. |year=1995}}{{page needed|date=April 2015 }}</ref> | ||
[[Gough Island]] in the South Atlantic is used by 20 species of seabirds for breeding, including almost all of the world's [[Tristan albatross]] (''Diomedea dabbenena'') and [[Atlantic petrel]] (''Pterodroma incerta''). Until house mice arrived on the island in the 19th century with sailors, the birds did not have any mammalian predators. The mice have since grown unusually large and have learned to attack [[albatross]] chicks, which can be 90 cm tall, but are largely immobile, by working in groups and gnawing on them until they bleed to death.<ref>{{cite journal|vauthors=Wanless RM, Angel A, Cuthbert RJ, Hilton GM, Ryan PG|title=Can predation by invasive mice drive seabird extinctions?|journal=Biology Letters|volume=3|issue =3|pages=241–4|date=June 2007|pmid=17412667|pmc=2464706|doi=10.1098/rsbl.2007.0120}}</ref> | [[Gough Island]] in the South Atlantic is used by 20 species of seabirds for breeding, including almost all of the world's [[Tristan albatross]] (''Diomedea dabbenena'') and [[Atlantic petrel]] (''Pterodroma incerta''). Until house mice arrived on the island in the 19th century with sailors, the birds did not have any mammalian predators. The mice have since grown unusually large and have learned to attack [[albatross]] chicks, which can be 90 cm tall, but are largely immobile, by working in groups and gnawing on them until they bleed to death.<ref>{{cite journal |vauthors=Wanless RM, Angel A, Cuthbert RJ, Hilton GM, Ryan PG |title=Can predation by invasive mice drive seabird extinctions? |journal=Biology Letters |volume=3 |issue=3 |pages=241–4 |date=June 2007 |pmid=17412667 |pmc=2464706 |doi=10.1098/rsbl.2007.0120 }}</ref> | ||
In the grain belt of southeastern Australia, the introduced subspecies ''Mus musculus domesticus'' breed so successfully, every three years or so they reach plague proportions, achieving densities of 1000 per hectare and causing massive disruption to communities, and losses to agriculture of A$36 million annually.<ref>{{cite web|url=http://archive.industry.gov.au/Biotechnologyonline.gov.au/enviro/mice.html|title=Mice: a case study|work=Biotechnology Australia|publisher=Commonwealth of Australia|access-date=April | In the grain belt of southeastern Australia, the introduced subspecies ''Mus musculus domesticus'' breed so successfully, every three years or so they reach plague proportions, achieving densities of 1000 per hectare and causing massive disruption to communities, and losses to agriculture of A$36 million annually.<ref>{{cite web |url=http://archive.industry.gov.au/Biotechnologyonline.gov.au/enviro/mice.html |title=Mice: a case study |work=Biotechnology Australia |publisher=Commonwealth of Australia |access-date=25 April 2015 |archive-date=4 April 2015 |archive-url=https://web.archive.org/web/20150404001251/http://archive.industry.gov.au/Biotechnologyonline.gov.au/enviro/mice.html |url-status=dead }}</ref> | ||
===As a model organism=== | ===As a model organism=== | ||
| Line 212: | Line 213: | ||
[[File:Muizenkooi met houten muizen (3).JPG|thumb|right|An individually ventilated and sealed cage for laboratory mice]] | [[File:Muizenkooi met houten muizen (3).JPG|thumb|right|An individually ventilated and sealed cage for laboratory mice]] | ||
Mice are the most commonly used mammalian laboratory animal, due to their relatively close relationship, and associated high [[homology (biology)|homology]], with humans, their ease in maintenance and handling, and their high rate of reproduction. Laboratory mice typically belong to standardized inbred strains selected for the stability or clarity of specific harmful mutations. This allows research with laboratory mice to easily restrict genetic and biological variables, making them very useful model organisms in genetic and medicinal research.<ref>{{cite web|url=http://www.informatics.jax.org/greenbook/frames/frame11.shtml|title=MGI — Biology of the Laboratory Mouse|publisher=Informatics.jax.org|access-date=2019 | Mice are the most commonly used mammalian laboratory animal, due to their relatively close relationship, and associated high [[homology (biology)|homology]], with humans, their ease in maintenance and handling, and their high rate of reproduction. Laboratory mice typically belong to standardized inbred strains selected for the stability or clarity of specific harmful mutations. This allows research with laboratory mice to easily restrict genetic and biological variables, making them very useful model organisms in genetic and medicinal research.<ref>{{cite web |url=http://www.informatics.jax.org/greenbook/frames/frame11.shtml |title=MGI — Biology of the Laboratory Mouse |publisher=Informatics.jax.org |access-date=6 February 2019 }}</ref> Mice have been used in scientific research since the 1650s.<ref>{{cite journal |vauthors=d'Isa R, Fasano S, Brambilla R |title=Editorial: Animal-friendly methods for rodent behavioral testing in neuroscience research |journal=Frontiers in Behavioral Neuroscience |volume=18 |pages=1431310 |date=June 2024 |pmid=38983871 |pmc=11232432 |doi=10.3389/fnbeh.2024.1431310 |doi-access=free }}</ref> | ||
===In folk culture=== | ===In folk culture=== | ||
Importance of mice as a house and agricultural pest resulted in a development of a variety of mouse-related rituals and stories in world's cultures. The [[Ancient Egyptians]] had a story about "The mouse as [[Vizier (Ancient Egypt)|vizier]]".<ref>[http://www.reshafim.org.il/ad/egypt/texts/mouse_as_vizier.htm The mouse as vizier], sourced to: Emma Brunner-Traut, ''Tiergeschichten aus dem Pharaonenland'', Mainz, Zabern, 2000.</ref> | Importance of mice as a house and agricultural pest resulted in a development of a variety of mouse-related rituals and stories in world's cultures. The [[Ancient Egyptians]] had a story about "The mouse as [[Vizier (Ancient Egypt)|vizier]]".<ref>[http://www.reshafim.org.il/ad/egypt/texts/mouse_as_vizier.htm The mouse as vizier], sourced to: Emma Brunner-Traut, ''Tiergeschichten aus dem Pharaonenland'', Mainz, Zabern, 2000.</ref> | ||
Many [[South Slavs]] had a traditional annual "Mouse Day" celebration. In the eastern Balkans (most of Bulgaria, [[North Macedonia]], the [[Torlakian dialect|Torlak]] districts of [[Serbia]]), the "Mouse Day" ({{langx|bg|Миши ден, Мишин ден}}) was celebrated on October | Many [[South Slavs]] had a traditional annual "Mouse Day" celebration. In the eastern Balkans (most of Bulgaria, [[North Macedonia]], the [[Torlakian dialect|Torlak]] districts of [[Serbia]]), the "Mouse Day" ({{langx|bg|Миши ден, Мишин ден}}) was celebrated on 9 October of the [[Julian calendar]] (corresponds to 27 October of the Gregorian calendar in the 20th and 21st centuries), the next day after the feast of [[Demetrius of Thessaloniki|Saint Demetrius]]. In the western Balkans ([[Bosnia]], [[Croatia]]), the Mouse Day would usually be celebrated in the spring, during the [[Maslenitsa]] week or early in the [[Lent]].<ref>{{cite book |url=http://www.kroraina.com/knigi/ap2/ap_2_1.htm |title=Этнолингвистическая география Южной Славии |trans-title=Ethnolinguistic Geography of the South Slav Lands |author=Plotnikova, Anna Arkadievna (Анна Аркадьевна Плотникова) |publisher=Indrik |place=Moscow |year=2004 |isbn=978-5857592878 |pages=64–68 |language=ru }}</ref> | ||
==See also== | ==See also== | ||
*[[Woolly mouse]] | * [[Woolly mouse]] | ||
*''[[Myobia musculi]]'', common [[mite]] found in fur of house mouse | * ''[[Myobia musculi]]'', common [[mite]] found in fur of house mouse | ||
==References== | ==References== | ||
{{Reflist|33em|refs= | {{Reflist|33em|refs= | ||
<ref name=Gregory>{{cite journal|vauthors=Gregory SG, Sekhon M, Schein J, Zhao S, Osoegawa K, Scott CE, Evans RS, Burridge PW, Cox TV, Fox CA, Hutton RD, Mullenger IR, Phillips KJ, Smith J, Stalker J, Threadgold GJ, Birney E, Wylie K, Chinwalla A, Wallis J, Hillier L, Carter J, Gaige T, Jaeger S, Kremitzki C, Layman D, Maas J, McGrane R, Mead K, Walker R, Jones S, Smith M, Asano J, Bosdet I, Chan S, Chittaranjan S, Chiu R, Fjell C, Fuhrmann D, Girn N, Gray C, Guin R, Hsiao L, Krzywinski M, Kutsche R, Lee SS, Mathewson C, McLeavy C, Messervier S, Ness S, Pandoh P, Prabhu AL, Saeedi P, Smailus D, Spence L, Stott J, Taylor S, Terpstra W, Tsai M, Vardy J, Wye N, Yang G, Shatsman S, Ayodeji B, Geer K, Tsegaye G, Shvartsbeyn A, Gebregeorgis E, Krol M, Russell D, Overton L, Malek JA, Holmes M, Heaney M, Shetty J, Feldblyum T, Nierman WC, Catanese JJ, Hubbard T, Waterston RH, Rogers J, de Jong PJ, Fraser CM, Marra M, McPherson JD, Bentley DR|display-authors=6|title=A physical map of the mouse genome|journal=Nature|volume=418|issue=6899|pages=743–50|date=August 2002|pmid=12181558|doi=10.1038/nature00957|bibcode=2002Natur.418..743G|s2cid=4325788}}</ref> | <ref name=Gregory>{{cite journal |vauthors=Gregory SG, Sekhon M, Schein J, Zhao S, Osoegawa K, Scott CE, Evans RS, Burridge PW, Cox TV, Fox CA, Hutton RD, Mullenger IR, Phillips KJ, Smith J, Stalker J, Threadgold GJ, Birney E, Wylie K, Chinwalla A, Wallis J, Hillier L, Carter J, Gaige T, Jaeger S, Kremitzki C, Layman D, Maas J, McGrane R, Mead K, Walker R, Jones S, Smith M, Asano J, Bosdet I, Chan S, Chittaranjan S, Chiu R, Fjell C, Fuhrmann D, Girn N, Gray C, Guin R, Hsiao L, Krzywinski M, Kutsche R, Lee SS, Mathewson C, McLeavy C, Messervier S, Ness S, Pandoh P, Prabhu AL, Saeedi P, Smailus D, Spence L, Stott J, Taylor S, Terpstra W, Tsai M, Vardy J, Wye N, Yang G, Shatsman S, Ayodeji B, Geer K, Tsegaye G, Shvartsbeyn A, Gebregeorgis E, Krol M, Russell D, Overton L, Malek JA, Holmes M, Heaney M, Shetty J, Feldblyum T, Nierman WC, Catanese JJ, Hubbard T, Waterston RH, Rogers J, de Jong PJ, Fraser CM, Marra M, McPherson JD, Bentley DR |display-authors=6 |title=A physical map of the mouse genome |journal=Nature |volume=418 |issue=6899 |pages=743–50 |date=August 2002 |pmid=12181558 |doi=10.1038/nature00957 |bibcode=2002Natur.418..743G |s2cid=4325788 }}</ref> | ||
<ref name="Mouse Genome Sequencing Consortium">{{cite journal|vauthors=Waterston RH, Lindblad-Toh K, Birney E, Rogers J, Abril JF, Agarwal P, Agarwala R, Ainscough R, Alexandersson M, An P, Antonarakis SE, Attwood J, Baertsch R, Bailey J, Barlow K, Beck S, Berry E, Birren B, Bloom T, Bork P, Botcherby M, Bray N, Brent MR, Brown DG, Brown SD, Bult C, Burton J, Butler J, Campbell RD, Carninci P, Cawley S, Chiaromonte F, Chinwalla AT, Church DM, Clamp M, Clee C, Collins FS, Cook LL, Copley RR, Coulson A, Couronne O, Cuff J, Curwen V, Cutts T, Daly M, David R, Davies J, Delehaunty KD, Deri J, Dermitzakis ET, Dewey C, Dickens NJ, Diekhans M, Dodge S, Dubchak I, Dunn DM, Eddy SR, Elnitski L, Emes RD, Eswara P, Eyras E, Felsenfeld A, Fewell GA, Flicek P, Foley K, Frankel WN, Fulton LA, Fulton RS, Furey TS, Gage D, Gibbs RA, Glusman G, Gnerre S, Goldman N, Goodstadt L, Grafham D, Graves TA, Green ED, Gregory S, Guigó R, Guyer M, Hardison RC, Haussler D, Hayashizaki Y, Hillier LW, Hinrichs A, Hlavina W, Holzer T, Hsu F, Hua A, Hubbard T, Hunt A, Jackson I, Jaffe DB, Johnson LS, Jones M, Jones TA, Joy A, Kamal M, Karlsson EK, Karolchik D, Kasprzyk A, Kawai J, Keibler E, Kells C, Kent WJ, Kirby A, Kolbe DL, Korf I, Kucherlapati RS, Kulbokas EJ, Kulp D, Landers T, Leger JP, Leonard S, Letunic I, Levine R, Li J, Li M, Lloyd C, Lucas S, Ma B, Maglott DR, Mardis ER, Matthews L, Mauceli E, Mayer JH, McCarthy M, McCombie WR, McLaren S, McLay K, McPherson JD, Meldrim J, Meredith B, Mesirov JP, Miller W, Miner TL, Mongin E, Montgomery KT, Morgan M, Mott R, Mullikin JC, Muzny DM, Nash WE, Nelson JO, Nhan MN, Nicol R, Ning Z, Nusbaum C, O'Connor MJ, Okazaki Y, Oliver K, Overton-Larty E, Pachter L, Parra G, Pepin KH, Peterson J, Pevzner P, Plumb R, Pohl CS, Poliakov A, Ponce TC, Ponting CP, Potter S, Quail M, Reymond A, Roe BA, Roskin KM, Rubin EM, Rust AG, Santos R, Sapojnikov V, Schultz B, Schultz J, Schwartz MS, Schwartz S, Scott C, Seaman S, Searle S, Sharpe T, Sheridan A, Shownkeen R, Sims S, Singer JB, Slater G, Smit A, Smith DR, Spencer B, Stabenau A, Stange-Thomann N, Sugnet C, Suyama M, Tesler G, Thompson J, Torrents D, Trevaskis E, Tromp J, Ucla C, Ureta-Vidal A, Vinson JP, Von Niederhausern AC, Wade CM, Wall M, Weber RJ, Weiss RB, Wendl MC, West AP, Wetterstrand K, Wheeler R, Whelan S, Wierzbowski J, Willey D, Williams S, Wilson RK, Winter E, Worley KC, Wyman D, Yang S, Yang SP, Zdobnov EM, Zody MC, Lander ES|display-authors=6|title=Initial sequencing and comparative analysis of the mouse genome|journal=Nature|volume=420|issue=6915|pages=520–62|date=December 2002|pmid=12466850|doi=10.1038/nature01262|bibcode=2002Natur.420..520W|doi-access=free}}</ref> | <ref name="Mouse Genome Sequencing Consortium">{{cite journal |vauthors=Waterston RH, Lindblad-Toh K, Birney E, Rogers J, Abril JF, Agarwal P, Agarwala R, Ainscough R, Alexandersson M, An P, Antonarakis SE, Attwood J, Baertsch R, Bailey J, Barlow K, Beck S, Berry E, Birren B, Bloom T, Bork P, Botcherby M, Bray N, Brent MR, Brown DG, Brown SD, Bult C, Burton J, Butler J, Campbell RD, Carninci P, Cawley S, Chiaromonte F, Chinwalla AT, Church DM, Clamp M, Clee C, Collins FS, Cook LL, Copley RR, Coulson A, Couronne O, Cuff J, Curwen V, Cutts T, Daly M, David R, Davies J, Delehaunty KD, Deri J, Dermitzakis ET, Dewey C, Dickens NJ, Diekhans M, Dodge S, Dubchak I, Dunn DM, Eddy SR, Elnitski L, Emes RD, Eswara P, Eyras E, Felsenfeld A, Fewell GA, Flicek P, Foley K, Frankel WN, Fulton LA, Fulton RS, Furey TS, Gage D, Gibbs RA, Glusman G, Gnerre S, Goldman N, Goodstadt L, Grafham D, Graves TA, Green ED, Gregory S, Guigó R, Guyer M, Hardison RC, Haussler D, Hayashizaki Y, Hillier LW, Hinrichs A, Hlavina W, Holzer T, Hsu F, Hua A, Hubbard T, Hunt A, Jackson I, Jaffe DB, Johnson LS, Jones M, Jones TA, Joy A, Kamal M, Karlsson EK, Karolchik D, Kasprzyk A, Kawai J, Keibler E, Kells C, Kent WJ, Kirby A, Kolbe DL, Korf I, Kucherlapati RS, Kulbokas EJ, Kulp D, Landers T, Leger JP, Leonard S, Letunic I, Levine R, Li J, Li M, Lloyd C, Lucas S, Ma B, Maglott DR, Mardis ER, Matthews L, Mauceli E, Mayer JH, McCarthy M, McCombie WR, McLaren S, McLay K, McPherson JD, Meldrim J, Meredith B, Mesirov JP, Miller W, Miner TL, Mongin E, Montgomery KT, Morgan M, Mott R, Mullikin JC, Muzny DM, Nash WE, Nelson JO, Nhan MN, Nicol R, Ning Z, Nusbaum C, O'Connor MJ, Okazaki Y, Oliver K, Overton-Larty E, Pachter L, Parra G, Pepin KH, Peterson J, Pevzner P, Plumb R, Pohl CS, Poliakov A, Ponce TC, Ponting CP, Potter S, Quail M, Reymond A, Roe BA, Roskin KM, Rubin EM, Rust AG, Santos R, Sapojnikov V, Schultz B, Schultz J, Schwartz MS, Schwartz S, Scott C, Seaman S, Searle S, Sharpe T, Sheridan A, Shownkeen R, Sims S, Singer JB, Slater G, Smit A, Smith DR, Spencer B, Stabenau A, Stange-Thomann N, Sugnet C, Suyama M, Tesler G, Thompson J, Torrents D, Trevaskis E, Tromp J, Ucla C, Ureta-Vidal A, Vinson JP, Von Niederhausern AC, Wade CM, Wall M, Weber RJ, Weiss RB, Wendl MC, West AP, Wetterstrand K, Wheeler R, Whelan S, Wierzbowski J, Willey D, Williams S, Wilson RK, Winter E, Worley KC, Wyman D, Yang S, Yang SP, Zdobnov EM, Zody MC, Lander ES |display-authors=6 |title=Initial sequencing and comparative analysis of the mouse genome |journal=Nature |volume=420 |issue=6915 |pages=520–62 |date=December 2002 |pmid=12466850 |doi=10.1038/nature01262 |bibcode=2002Natur.420..520W |doi-access=free }}</ref> | ||
}} | }} | ||
==Further reading== | ==Further reading== | ||
*{{cite book|author=Nyby, John G.|name-list-style=vanc|year=2001|chapter=Auditory Communication among Adults |chapter-url=https://books.google.com/books?id=EEOyWhWn8hgC&pg=PA3|pages=3–18|editor=Willott, James F.|title=Handbook of Mouse Auditory Research: From Behavior to Molecular Biology|publisher=CRC Press|isbn=978-1-4200-3873-6}} | * {{cite book |author=Nyby, John G. |name-list-style=vanc |year=2001 |chapter=Auditory Communication among Adults |chapter-url=https://books.google.com/books?id=EEOyWhWn8hgC&pg=PA3 |pages=3–18 |editor=Willott, James F. |title=Handbook of Mouse Auditory Research: From Behavior to Molecular Biology |publisher=CRC Press |isbn=978-1-4200-3873-6}} | ||
==External links== | ==External links== | ||
| Line 238: | Line 239: | ||
===Taxonomy=== | ===Taxonomy=== | ||
*[http://www.findmice.org/ findmice.org] | * [http://www.findmice.org/ findmice.org] | ||
===Genetics=== | ===Genetics=== | ||
*[http://www.ensembl.org/Mus_musculus/ Ensembl ''Mus musculus'' genome browser], from the [[Ensembl]] Project | * [http://www.ensembl.org/Mus_musculus/ Ensembl ''Mus musculus'' genome browser], from the [[Ensembl]] Project | ||
*[http://vega.sanger.ac.uk/Mus_musculus Vega ''Mus musculus'' genome browser], includes NOD mouse sequence and annotation | * [http://vega.sanger.ac.uk/Mus_musculus Vega ''Mus musculus'' genome browser], includes NOD mouse sequence and annotation | ||
*{{UCSC genomes|mm10}} | * {{UCSC genomes|mm10}} | ||
===Media=== | ===Media=== | ||
*[http://www.digimorph.org/specimens/Mus_musculus/ Pictures, movies and applets showing the anatomy of ''Mus musculus''], from www.digimorph.org | * [http://www.digimorph.org/specimens/Mus_musculus/ Pictures, movies and applets showing the anatomy of ''Mus musculus''], from www.digimorph.org | ||
*[https://web.archive.org/web/20080509105126/http://www.arkive.org/species/ARK/mammals/Mus_musculus/ Arkive] Photographs. Short text. | * [https://web.archive.org/web/20080509105126/http://www.arkive.org/species/ARK/mammals/Mus_musculus/ Arkive] Photographs. Short text. | ||
===Further reading=== | ===Further reading=== | ||
*[http://www.nature.com/nature/mousegenome/ Nature Mouse Special 2002] | * [http://www.nature.com/nature/mousegenome/ Nature Mouse Special 2002] | ||
*[https://web.archive.org/web/20050313011817/http://www.ahsc.arizona.edu/uac/notes/classes/rodentbio/rodentbio.html Biology of Laboratory Rodents] by David G. Besselsen | * [https://web.archive.org/web/20050313011817/http://www.ahsc.arizona.edu/uac/notes/classes/rodentbio/rodentbio.html Biology of Laboratory Rodents] by David G. Besselsen | ||
*[http://www.pestworld.org/pest-guide/rodents/house-mice/ House Mouse Fact Sheet] from the [[National Pest Management Association]] with information on habits, habitat and health threats | * [http://www.pestworld.org/pest-guide/rodents/house-mice/ House Mouse Fact Sheet] from the [[National Pest Management Association]] with information on habits, habitat and health threats | ||
*[http://animaldiversity.ummz.umich.edu/site/accounts/information/Mus_musculus.html Comprehensive house mouse information, including pictures], by the University of Michigan Museum of Zoology | * [http://animaldiversity.ummz.umich.edu/site/accounts/information/Mus_musculus.html Comprehensive house mouse information, including pictures], by the University of Michigan Museum of Zoology | ||
*[http://www.ratbehavior.org/RatsMice.htm Some information on muricide] | * [http://www.ratbehavior.org/RatsMice.htm Some information on muricide] | ||
*[http://www.mcmaster.ca/inabis98/brudzynski/white0360/two.html Vocalizations during copulation] | * [http://www.mcmaster.ca/inabis98/brudzynski/white0360/two.html Vocalizations during copulation] | ||
{{Model Organisms}} | {{Model Organisms}} | ||
Revision as of 10:24, 30 June 2025
Template:Short description Template:Use dmy dates Template:Speciesbox
The house mouse (Mus musculus) is a small mammal of the rodent family Muridae, characteristically having a pointed snout, large rounded ears, and a long and almost hairless tail. It is one of the most abundant species of the genus Mus. Although a wild animal, the house mouse has benefited significantly from associating with human habitation to the point that truly wild populations are significantly less common than the synanthropic populations near human activity.
The house mouse has been domesticated as the pet or fancy mouse, and as the laboratory mouse, which is one of the most important model organisms in biology and medicine. The complete mouse reference genome was sequenced in 2002.[1][2]
Characteristics
House mice have an adult body length (nose to base of tail) of Script error: No such module "convert". and a tail length of Script error: No such module "convert".. The weight is typically Script error: No such module "convert".. In the wild they vary in color from grey and light brown to black (individual hairs are actually agouti coloured), but domesticated fancy mice and laboratory mice are produced in many colors ranging from white to champagne to pink.[3] They have short hair and some, but not all, sub-species have a light belly.[3] The ears and tail have little hair. The hind feet are short compared to Apodemus mice, only Script error: No such module "convert". long; the normal gait is a run with a stride of about Script error: No such module "convert"., though they can jump vertically up to Script error: No such module "convert"..[4] The voice is a high-pitched squeak.[5][6] House mice thrive under a variety of conditions; they are found in and around homes and commercial structures, as well as in open fields and agricultural lands.[7]
Newborn males and females can be distinguished on close examination as the anogenital distance in males is about double that of the female.[8] From the age of about 10 days, females have five pairs of mammary glands and nipples; males have no nipples.[9] When sexually mature, the most striking and obvious difference is the presence of testicles on the males. These are large compared to the rest of the body and can be retracted into the body.[10]
The tail, which is used for balance,[11][12][13] has only a thin covering of hair as it is the main peripheral organ of heat loss in thermoregulation[12] along with—to a lesser extent—the hairless parts of the paws and ears. Blood flow to the tail can be precisely controlled in response to changes in ambient temperature using a system of arteriovenous anastomoses to increase the temperature of the skin on the tail by as much as Script error: No such module "convert". to lose body heat.[14] Tail length varies according to the environmental temperature of the mouse during postnatal development, so mice living in colder regions tend to have shorter tails.[3] The tail is also used for balance when the mouse is climbing or running, or as a base when the animal stands on its hind legs (a behaviour known as tripoding), and to convey information about the dominance status of an individual in encounters with other mice.[15]
In addition to the regular pea-sized thymus organ in the chest, house mice have a second functional pinhead-sized thymus organ in the neck next to the trachea.[16]
Taxonomy and subspecies
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Mice are mammals of the Glires clade, which means they are amongst the closest relatives of humans other than lagomorphs, treeshrews, flying lemurs and other primates.
The three widely accepted subspecies are increasingly treated as distinct species by some:[17][18]
- Southeastern Asian house mouse (Mus musculus castaneus) (southern and southeastern Asia)
- Western European house mouse (Mus musculus domesticus); includes the fancy mouse and the laboratory mouse (Western Europe, North America, South America, Africa and Oceania)
- Eastern European house mouse (Mus musculus musculus) (Eastern Europe and northern Asia)
Two additional subspecies have been recognized more recently:[18]
- Southwestern Asian house mouse (Mus musculus bactrianus) (southwestern and Central Asia). However, due to significant genetic similarity observed between (Mus musculus bactrianus) and Mus musculus castaneus, the subspecies designation for Mus musculus bactrianus has now been questioned.[19]
- pygmy house mouse (Mus musculus gentilulus) (the Arabian Peninsula and Madagascar)[20]
Many more subspecies' names have been given to house mice, but these are now regarded as synonyms of the five subspecies. Some populations are hybrids of different subspecies, including the Japanese house mouse (M. m. molossinus).[18] A notable region of hybridization is a region in general Europe where M. m. domesticus and M. m. musculus are often found to hybridize.[21] However, male hybrid mice typically experience hybrid sterility, which maintains reproductive separation between the two subspecies.[22]
Chromosomal races
The standard species karyotype is composed of 40 chromosomes. Within Western Europe there are numerous populations – chromosomal races – with a reduced chromosome count arising from Robertsonian fusion.
Evolution
Suzuki et al., 2013 confirms the theory that M. musculus originates in Southwestern Asia and identifies 5 subspecies and their origins: musculus in northern Eurasia, castaneus in India and Southeast Asia, a previously unknown subspecies from Nepal, domesticus in western Europe, and gentilulus in Yemen.[23]
A recent study using 89 whole-genome sequences revealed that the modern day Mus musculus castaneus emerged from an ancestral Mus musculus population in Indian subcontinent some time around 700 kya. From there, this ancestral population migrated to Iran around 360 kya to form Mus musculus domesticus and then to Afghanistan around 260 kya to form Mus musculus musculus.[24]
Behavior
House mice usually run, walk, or stand on all fours, but when eating, fighting, or orienting themselves, they rear up on their hind legs with additional support from the tail – a behavior known as "tripoding". Mice are good jumpers, climbers, and swimmers, and are generally considered to be thigmotactic, i.e. usually attempt to maintain contact with vertical surfaces.Script error: No such module "Unsubst".
Mice are mostly crepuscular or nocturnal; they are averse to bright lights. The average sleep time of a captive house mouse is reported to be 12.5 hours per day.Script error: No such module "Unsubst". They live in a wide variety of hidden places near food sources, and construct nests from various soft materials. Mice are territorial, and one dominant male usually lives together with several females and young mice. Dominant males respect each other's territories and normally enter another's territory only if it is vacant. If two or more males are housed together in a cage, they often become aggressive unless they have been raised together from birth.Script error: No such module "Unsubst".
House mice primarily feed on plant matter, but are omnivorous.[25] They eat their own faeces to acquire nutrients produced by bacteria in their intestines.[26] House mice, like most other rodents, do not vomit.[27]
Mice are generally afraid of rats which often kill and eat them, a behavior known as muricide. Despite this, free-living populations of rats and mice do exist together in forest areas in New Zealand, North America, and elsewhere. House mice are generally poor competitors and in most areas cannot survive away from human settlements in areas where other small mammals, such as wood mice, are present.[28] However, in some areas (such as Australia), mice are able to coexist with other small rodent species.[29]
Social behavior
The social behavior of the house mouse is not rigidly fixed into species-specific patterns but is instead adaptable to the environmental conditions, such as the availability of food and space.[30][31] This adaptability allows house mice to inhabit diverse areas ranging from sandy dunes to apartment buildings.[30]
House mice have two forms of social behaviour, the expression of which depends on the environmental context. House mice in buildings and other urbanized areas with close proximity to humans are known as commensal.[30] Commensal mice populations often have an excessive food source resulting in high population densities and small home ranges. This causes a switch from territorial behaviour to a hierarchy of individuals.[30][32] When populations have an excess of food, there is less female-female aggression, which usually occurs to gain access to food or to prevent infanticide.[30] Male-male aggression occurs in commensal populations, mainly to defend female mates and protect a small territory.[30][31] The high level of male-male aggression, with a low female-female aggression level is common in polygamous populations.[33] The social unit of commensal house mouse populations generally consists of one male and two or more females, usually related.[33][34] These groups breed cooperatively, with the females communally nursing. This cooperative breeding and rearing by related females helps increase reproductive success. When no related females are present, breeding groups can form from non-related females.[34]
In open areas such as shrubs and fields, the house mouse population is known as noncommensal. These populations are often limited by water or food supply and have large territories.[31] Female-female aggression in the noncommensal house mouse populations is much higher, reaching a level generally attributed to free-ranging species. Male aggression is also higher in noncommensal populations. In commensal populations, males come into contact with other males quite frequently due to high population densities and aggression must be mediated or the risk of injury becomes too great.[30]
Both commensal and noncommensal house mouse males aggressively defend their territory and act to exclude all intruders. Males mark their territory by scent marking with urine. In marked territories, intruders showed significantly lower aggression than the territory residents.[31] House mice show a male-biased dispersal; males generally leave their birth sites and migrate to form new territories whereas females generally stay and are opportunistic breeders rather than seasonal.[35]
Senses and communication
Vision
The visual apparatus of mice is basically similar to that of humans but differs in that they are dichromats and have only two types of cone cells whereas humans are trichromats and have three. This means that mice do not perceive some of the colors in the human visual spectrum.[36] However, the ventral area of the mouse retina has a much greater density of ultraviolet-sensitive cones than other areas of the retina, although the biological significance of this structure is unknown.[37][38][39] In 2007, mice genetically engineered to produce the third type of cone were shown to be able to distinguish a range of colors similar to that perceived by tetrachromats.[36]
Olfaction
House mice also rely on pheromones for social communication, some of which are produced by the preputial glands of both sexes. The tear fluid and urine of male mice also contains pheromones, such as major urinary proteins.[40][41] Mice detect pheromones mainly with the vomeronasal organ (Jacobson's organ), located at the bottom of the nose.
The urine of house mice, especially that of males, has a characteristic strong odor. At least 10 different compounds, such as alkanes, alcohols, etc., are detectable in the urine. Among them, five compounds are specific to males, namely 3-cyclohexene-1-methanol, aminotriazole (3-amino-s-triazole), 4-ethyl phenol, 3-ethyl-2,7-dimethyl octane and 1-iodoundecane.[42]
Odours from adult males or from pregnant or lactating females can speed up or retard sexual maturation in juvenile females and synchronise reproductive cycles in mature females (i.e. the Whitten effect). Odours of unfamiliar male mice may terminate pregnancies, i.e. the Bruce effect.
Tactile
Mice can sense surfaces and air movements with their whiskers which are also used during thigmotaxis. If mice are blind from birth, super-normal growth of the vibrissae occurs presumably as a compensatory response.[43] Conversely, if the vibrissae are absent, the use of vision is intensified.[44]
Life cycle and reproduction
Female house mice have an estrous cycle about four to six days long, with estrus itself lasting less than a day. If several females are held together under crowded conditions, they will often not have an estrus at all. If they are then exposed to male urine, they will come into estrus after 72 hours.Script error: No such module "Unsubst".
Male house mice court females by emitting characteristic ultrasonic calls in the 30 kHz–110 kHz Script error: No such module "Unsubst". range. The calls are most frequent during courtship when the male is sniffing and following the female; however, the calls continue after mating has begun, at which time the calls are coincident with mounting behaviour. Males can be induced to emit these calls by female pheromones. The vocalizations appear to differ between individuals and have been compared to bird songs because of their complexity.[45] While females have the capability to produce ultrasonic calls, they typically do not do so during mating behaviour.Script error: No such module "Unsubst".
Following copulation, female mice will normally develop a mating plug which prevents further copulation. The plug is not necessary for pregnancy initiation, as this will also occur without the plug. The presence or absence of the plug will not affect litter size either.[46] This plug stays in place for some 24 hours. The gestation period is about 19–21 days, and they give birth to a litter of 3–14 young (average six to eight). One female can have 5 to 10 litters per year, so the mouse population can increase very quickly. Breeding occurs throughout the year. (However, animals living in the wild do not reproduce in the colder months, even though they do not hibernate.)Script error: No such module "Unsubst".
The pups are born blind and without fur or ears. The ears are fully developed by the fourth day, fur begins to appear at about six days and the eyes open around 13 days after birth; the pups are weaned at around 21 days. Females reach sexual maturity at about six weeks of age and males at about eight weeks, but both can copulate as early as five weeks.[47]
Polygamy
Although house mice can be either monogamous or polygamous, they are most commonly polygamous. They generally show characteristics of mate-defense polygyny in that males are highly territorial and protective of their mates, while females are less agonistic.[48] The communal nursing groups that result from these behaviors lead to lower numbers of infanticide since more females are able to protect greater numbers of offspring.[49]
Evolutionary and behavioural consequences
Both evolutionary and behavioral consequences result from the polygamous nature of the house mouse. One consequence is the paternal investment, which is lower in polygamous mice than in mice that are monogamous.[50] This occurs due to the fact that males spend more time involved in sexual competition than do females, leaving less time for paternal care.[50] Polygamous male house mice spend less time alone with pups.[50] They are also less likely and slower to retrieve lost pups than males of monogamous mice.[50] In contrast, the maternal investment is similar between female mice that have mated once versus multiply.[50]
The polygamous behavior of female house mice promotes sperm competition, which affects both male and female evolutionary fitness.[46] Females who mate with multiple males tend to produce both pups in greater numbers,[46] and with higher survival rates,[51] increasing female fitness. Sperm competition that arises from polygamy favors males with faster, more motile sperm in higher numbers, increasing male fitness.[46] The competitive aspect of insemination increases the frequency of polyandrous events and fertilizations. Polyandry has evolved to increase reproductive success.[52] Male mating behavior is also affected in response to the practice of polygamous behavior. Compared to monogamous house mice, polygamous house mice mate for longer periods of time.[53] This behaviour allows for an increase in both the transfer of sperm and paternity success, which in turn increases male fitness.[53]
Polyandry
As opposed to polygyny, polyandrous behavior in females is the act of breeding with several males in the same season.[54] Variation in number of males that females mate with occurs among a population. Polyandrous behavior is a common mating pattern in the subspecies Mus musculus musculus as well as its relative Mus musculus domesticus.[54]
Polyandry occurs in 30% of all wild populations of house mice.[55] Litters from multiple sires tend to be more genetically diverse than litters of single sires.[54] Multiple paternity is also more common in larger populations than smaller populations, because there is a larger number of mates and more diverse mates to choose from.[55] Within a population, males and females show different levels of multiple mating. Females show bias toward unrelated males rather than related males during sexual selection, resulting in more genetically diverse offspring and a reduction of inbreeding depression.[52] Inbreeding depression increases genetic incompatibilities, levels of homozygosity, and the chance of expression of deleterious recessive alleles.[52] Polyandry has been shown to increase offspring survival compared to monandry.
Evolutionary consequences
The fitness of females increases in polyandrous lines due to more genetic diversity and greater litter size.[46]
Due to polyandry, males can be confused by the identity of new offspring.[56] Multiple mating by females and paternity confusion can decrease rates of infanticide.[56] If the males are uncertain if the offspring are theirs, they are less likely to kill the offspring.[56]
Intrauterine insemination causes an evolutionary consequence resulting from polyandrous behavior.[57] When multiple males mate with one female, there are multiple sets of sperm gametes in a female mouse. Offspring fertilized by multiple males can compete more strongly for mother's resources and can lead to a decrease in body size and variation in body size.[57]
Inbreeding avoidance
Since inbreeding is detrimental, it tends to be avoided. In the house mouse, the major urinary protein (MUP) gene cluster provides a highly polymorphic scent signal of genetic identity that appears to underlie kin recognition and inbreeding avoidance. Thus there are fewer matings between mice sharing MUP haplotypes than would be expected if there were random mating.[58] Another mechanism for avoiding inbreeding is evident when a female house mouse mates with multiple males. In such a case, there appears to be egg-driven sperm selection against sperm from related males.[59]
Genetics
As a model organism, a great deal is known about mouse genetics, with a major tool being the knockout mouse technique.
Life expectancy
House mice usually live less than one year in the wild, due to a high level of predation and exposure to harsh environments.[60] In protected environments, however, they often live two to three years. The Methuselah Mouse Prize is a competition to breed or engineer extremely long-lived laboratory mice. since 2005[update]Template:Dated maintenance category (articles)Script error: No such module "Check for unknown parameters"., the record holder was a genetically engineered mouse that lived for 1,819 days (7 days short of 5 years).[61] Another record holder that was kept in an enriched environment but did not receive any genetic, pharmacological, or dietary treatment lived for 1,551 days (Template:Years and days).[62][63]
Aging
In several different mouse strains, a significant increase was observed with age in 8-Oxo-2'-deoxyguanosine (8-oxo-dG) levels in nuclear DNA from liver, heart, brain, kidney, skeletal muscle and spleen.[64] This increase in DNA damage was attributed to an age related increase in the sensitivity of these tissues to oxidative stress.[64] Dietary restriction is known to increase the lifespan of rodents and to retard aging. Dietary restriction was found to significantly reduce the age-related accumulation of 8-oxo-dG levels in nuclear DNA of all tissues studied in mice.[64] Thus it was suggested that oxidative DNA damages that arise from normal cellular metabolism could be highly relevant to aging and the diseases of aging.[64] In another study, two types of DNA damage (8-hydroxy-2’-deoxyguanosine and DNA-protein crosslinks) were found to increase with age in mouse brain and liver.[65]
Mice and humans
History
House mice usually live in proximity to humans, in or around houses and/or fields. They are native to India,[66][67] and later they spread to the eastern Mediterranean about 13,000 BC, only spreading into the rest of Europe around 1000 BC.[68] This time lag is thought to be because the mice require agrarian human settlements above a certain size.[68] The house mouse first arrived in the Americas in the early sixteenth century. It was carried aboard on the ships of Spanish explorers and Conquistadors. About one hundred years later, it arrived in North America with French fur traders and English colonists. They have since been spread to all parts of the globe by humans.[69]
Many studies have been done on mouse phylogenies to reconstruct early human movements. For example, one study suggests the possibility of a previously unsuspected early link between Northern Europe and Madeira on the basis of the origin of Madeiran mice.[70] House mice were thought to be the primary reason for the domestication of cats.[71]
As pets
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The first written reference to mice kept as pets occurs in the Erya, the oldest extant Chinese dictionary, from a mention in an 1100 BC version.[72] Human domestication led to numerous strains of "fancy" or hobby mice with a variety of colours and a docile temperament.[73] Domestic varieties of the house mouse are bred as a food source for some carnivorous pet reptiles, birds, arthropods, and fish.[73] The effects of domestication can be rapid, with captive-reared mice differing in boldness and activity patterns compared to wild-caught mice after 4–5 generations in recent research.[74][75]
Mice as pests
Mice are widespread pest organisms, and one of the most common rodents to infest human buildings. They commonly forage outdoors during the spring and summer, but retreat into buildings through the autumn and winter to seek warmth and food. They typically feed on unattended food, leftovers and garden produce. Their foraging risks the contamination and degradation of food supplies, and can also spread other pests such as fleas, ticks, lice and mites.[76]
When infesting homes, house mice may pose a risk of damaging and compromising the structure of furniture and the building itself. They gnaw various materials to file down their growing teeth and keep the length under control. Common damage includes gnawed electrical wires, marks on wooden furniture and construction supporting elements, and textile damage.[77]
Mice and diseases
House mice can sometimes transmit diseases, contaminate food, and damage food packaging. Although the Centers for Disease Control and Prevention provides a list with diseases transmitted by rodents,[78] only a few of the diseases are transmitted through the house mouse.[79]
Lymphocytic choriomeningitis (LCMV) can be transmitted by mice, but is not a commonly reported infection in humans, though most infections are mild and are often never diagnosed.[80][81][82] Some concern exists that women should not be infected with LCMV during pregnancy.[83][84]
House mice are not usually a vector of human plague (bubonic plague) because they have fewer infestations with fleas than do rats, and because the fleas which house mice normally carry exhibit little tendency to bite humans rather than their natural host.[85]
Rickettsialpox, caused by the bacterium Rickettsia akari and similar to chickenpox, is spread by mice in general, but is very rare and generally mild and resolves within two or three weeks if untreated. No known deaths have resulted from the disease. Murine typhus (also called endemic typhus), caused by the bacterium Rickettsia typhi, is transmitted by the fleas that infest rats. While rat fleas are the most common vectors, cat fleas and mouse fleas are less common modes of transmission.[86] Endemic typhus is highly treatable with antibiotics. The U.S. CDC currently does not mention rickettsialpox or murine typhus on its website about diseases directly transmitted by rodents (in general).[78]
Leptospirosis is carried by a variety of wild and domestic animals including dogs, rats, swine, cattle, mice in general, and can be transmitted by the urine of an infected animal and is contagious as long as the urine is still moist.[87]
In Central Europe, the Dobriva sequence of hantavirus has been found in house mice. This is the most serious type of hanta that can infect humans.[88]
Mice contribute indirectly to the transmission of Lyme disease by acting as hosts for tick larvae.[89] When young ticks feed on infected mice, they acquire the bacteria responsible for the disease. As these ticks mature, they can transmit the infection to humans and other animals through subsequent bites, thereby playing a crucial role in the disease's ecological cycle.[90]
Invasive species
Mice have become an invasive species on islands to where they have spread during the period of European exploration and colonisation.[91]
New Zealand had no land mammals other than two species of bat prior to human occupation, and the house mouse is one of many species that have been introduced. Mice are responsible for a reduction in native bird species since they eat some of the same foods as birds. They are also known to kill lizards and have a large effect on native insects.[92]
Gough Island in the South Atlantic is used by 20 species of seabirds for breeding, including almost all of the world's Tristan albatross (Diomedea dabbenena) and Atlantic petrel (Pterodroma incerta). Until house mice arrived on the island in the 19th century with sailors, the birds did not have any mammalian predators. The mice have since grown unusually large and have learned to attack albatross chicks, which can be 90 cm tall, but are largely immobile, by working in groups and gnawing on them until they bleed to death.[93]
In the grain belt of southeastern Australia, the introduced subspecies Mus musculus domesticus breed so successfully, every three years or so they reach plague proportions, achieving densities of 1000 per hectare and causing massive disruption to communities, and losses to agriculture of A$36 million annually.[94]
As a model organism
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Mice are the most commonly used mammalian laboratory animal, due to their relatively close relationship, and associated high homology, with humans, their ease in maintenance and handling, and their high rate of reproduction. Laboratory mice typically belong to standardized inbred strains selected for the stability or clarity of specific harmful mutations. This allows research with laboratory mice to easily restrict genetic and biological variables, making them very useful model organisms in genetic and medicinal research.[95] Mice have been used in scientific research since the 1650s.[96]
In folk culture
Importance of mice as a house and agricultural pest resulted in a development of a variety of mouse-related rituals and stories in world's cultures. The Ancient Egyptians had a story about "The mouse as vizier".[97]
Many South Slavs had a traditional annual "Mouse Day" celebration. In the eastern Balkans (most of Bulgaria, North Macedonia, the Torlak districts of Serbia), the "Mouse Day" (Template:Langx) was celebrated on 9 October of the Julian calendar (corresponds to 27 October of the Gregorian calendar in the 20th and 21st centuries), the next day after the feast of Saint Demetrius. In the western Balkans (Bosnia, Croatia), the Mouse Day would usually be celebrated in the spring, during the Maslenitsa week or early in the Lent.[98]
See also
- Woolly mouse
- Myobia musculi, common mite found in fur of house mouse
References
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- ↑ a b the Rat and Mouse Club of America
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- ↑ "A previous study [1943] reported house mice naturally infected with R. typhi in the state of Georgia; however, no PCR-positive mice were detected in our study. Eruptions of mouse populations in the absence of rats have been implicated in several outbreaks of murine typhus; however, these observations were not supported by laboratory data." Script error: No such module "Citation/CS1".
- ↑ Script error: No such module "Citation/CS1".
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- ↑ Script error: No such module "citation/CS1".Script error: No such module "Unsubst".
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- ↑ The mouse as vizier, sourced to: Emma Brunner-Traut, Tiergeschichten aus dem Pharaonenland, Mainz, Zabern, 2000.
- ↑ Script error: No such module "citation/CS1".
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Further reading
- Script error: No such module "citation/CS1".
External links
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Taxonomy
Genetics
- Ensembl Mus musculus genome browser, from the Ensembl Project
- Vega Mus musculus genome browser, includes NOD mouse sequence and annotation
- Template:UCSC genomes
Media
- Pictures, movies and applets showing the anatomy of Mus musculus, from www.digimorph.org
- Arkive Photographs. Short text.
Further reading
- Nature Mouse Special 2002
- Biology of Laboratory Rodents by David G. Besselsen
- House Mouse Fact Sheet from the National Pest Management Association with information on habits, habitat and health threats
- Comprehensive house mouse information, including pictures, by the University of Michigan Museum of Zoology
- Some information on muricide
- Vocalizations during copulation
Template:Model Organisms Template:Murinae (Melasmothrix–Mus) Template:Taxonbar