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{{short description|Model for genetics of flower development}}
{{Redirect|ABC model|the model of attitudes used in psychology|Attitude (psychology)}}
[[File:ABC Model.svg|thumb|upright=2|ABC model of flower development guided by three groups of [[homeotic gene]]s.]]

The '''ABC model of flower development''' is a [[scientific model]] of the process by which [[flowering plant]]s produce a pattern of [[gene expression]] in [[meristem]]s that leads to the appearance of an organ oriented towards [[sexual reproduction]], a flower. There are three [[physiology|physiological]] developments that must occur in order for this to take place: firstly, the plant must pass from sexual immaturity into a sexually mature state (i.e. a transition towards flowering); secondly, the transformation of the [[apical meristem|apical meristem's]] function from a vegetative meristem into a floral meristem or [[inflorescence]]; and finally the growth of the flower's individual organs. The latter phase has been modelled using the '''ABC model''', which aims to describe the biological basis of the process from the perspective of [[molecular genetics|molecular]] and [[developmental genetics|developmental]] genetics.

An external [[stimulus (physiology)|stimulus]] is required in order to trigger the [[cellular differentiation|differentiation]] of the meristem into a flower meristem. This stimulus will activate [[mitosis|mitotic]] cell division in the apical meristem, particularly on its sides where new [[primordium|primordia]] are formed. This same stimulus will also cause the meristem to follow a [[biological development|developmental]] pattern that will lead to the growth of floral meristems as opposed to vegetative meristems. The main difference between these two types of meristem, apart from the obvious disparity between the objective organ, is the verticillate (or whorled) [[phyllotaxis]], that is, the absence of [[plant stem|stem]] elongation among the successive [[whorl (botany)|whorls or verticils]] of the primordium. These verticils follow an acropetal development, giving rise to [[sepal]]s, [[petal]]s, [[stamen]]s and [[carpel]]s. Another difference from vegetative axillary meristems is that the floral meristem is "determined", which means that, once differentiated, its cells will no longer [[cell cycle|divide]].<ref name="azcón-bieto">{{cite book| author = Azcón-Bieto | title = Fundamentos de fisiología vegetal | year = 2000 | publisher = McGraw-Hill/Interamericana de España, SAU | isbn = 978-84-486-0258-1|display-authors=etal}}{{page needed|date=April 2013}}</ref>

The identity of the organs present in the four floral verticils is a consequence of the interaction of at least three types of [[gene products]], each with distinct functions. According to the ABC model, functions A and C are required in order to determine the identity of the verticils of the [[perianth]] and the reproductive verticils, respectively. These functions are exclusive and the absence of one of them means that the other will determine the identity of all the floral verticils. The B function allows the differentiation of petals from sepals in the secondary verticil, as well as the differentiation of the stamen from the carpel on the tertiary verticil.

[[Johann Wolfgang von Goethe|Goethe]]'s '''foliar theory''' was formulated in the 18th century and it suggests that the constituent parts of a flower are structurally modified leaves, which are functionally specialized for reproduction or protection. The theory was first published in 1790 in the essay "Metamorphosis of Plants" ("''Versuch die Metamorphose der Pflanzen zu erklären''").<ref name="D2">{{cite journal |doi=10.1590/S1677-04202005000400001 |title=From leaf to flower: Revisiting Goethe's concepts on the ¨metamorphosis¨ of plants |year=2005 |last1=Dornelas |first1=Marcelo Carnier |last2=Dornelas |first2=Odair |journal=Brazilian Journal of Plant Physiology |volume=17 |issue=4|pages=335–344 |doi-access=free }}</ref> where Goethe wrote:

{{quote|"...we may equally well say that a stamen is a contracted petal, as that a petal is a stamen in a state of expansion; or that a sepal is a contracted stem leaf approaching a certain stage of refinement, as that a stem leaf is a sepal expanded by the influx of cruder saps".<ref>Goethe J.W. von (1790) Versuch die Metamorphose der Pflanzen zu erklaren. Gotha, Ettlinger; paragraph 120."</ref>}}

==Floral transition==

The [[Vegetative phase change|transition from]] the [[vegetative phase]] to a [[flower|reproductive phase]] involves a dramatic change in the plant's vital cycle, perhaps the most important one, as the process must be carried out correctly in order to guarantee that the plant produces [[kinship|descendants]]. This transition is characterised by the induction and development of the meristem of the inflorescence, which will produce a collection of flowers or one flower. This [[morphogenesis|morphogenetic]] change contains both endogenous and exogenous elements: For example, in order for the change to be initiated the plant must have a certain number of [[leaf|leaves]] and contain a certain level of total [[biomass]]. Certain environmental conditions are also required such as a characteristic [[photoperiod]]. [[Plant hormone]]s play an important part in the process, with the [[gibberellin]]s having a particularly important role.<ref name="blázquez">{{cite journal |pmid=9596637 |jstor=3870665 |year=1998 |last1=Blazquez |first1=MA |last2=Green |first2=R |last3=Nilsson |first3=O |last4=Sussman |first4=MR |last5=Weigel |first5=D |title=Gibberellins promote flowering of arabidopsis by activating the LEAFY promoter |volume=10 |issue=5 |pages=791–800 |pmc=144373 |journal=The Plant Cell |doi=10.1105/tpc.10.5.791}}</ref>

There are many [[signal transduction|signals]] that regulate the [[molecular biology]] of the process. The following three genes in ''[[Arabidopsis thaliana]]'' possess both common and independent functions in floral transition: ''FLOWERING LOCUS T'' (''FT''), ''LEAFY'' (''LFY''), ''SUPPRESSOR OF OVEREXPRESSION OF CONSTANS1'' (''SOC1'', also called ''AGAMOUS-LIKE20'').<ref>{{cite journal |doi=10.1038/35009125 |title=Integration of floral inductive signals in Arabidopsis |year=2000 |last1=Blázquez |first1=Miguel A. |last2=Weigel |first2=Detlef |journal=Nature |volume=404 |issue=6780 |pages=889–92 |pmid=10786797|bibcode=2000Natur.404..889B |s2cid=4373900 }}</ref> ''SOC1'' is a [[MADS-box]]-type gene, which integrates responses to photoperiod, [[vernalization]] and gibberellins.<ref name="blázquez" />

==Formation of the floral meristem or the inflorescence==

The [[meristem]] can be defined as the tissue or group of plant tissues that contain undifferentiated [[stem cells]], which are capable of producing any type of cell tissue. Their maintenance and development, both in the vegetative meristem or the meristem of the inflorescence is controlled by genetic [[cell fate determination]] mechanisms. This means that a number of genes will directly regulate, for example, the maintenance of the stem cell's characteristics (gene ''WUSCHEL'' or ''WUS''), and others will act via [[negative feedback]] mechanisms in order to inhibit a characteristic (gene ''CLAVATA'' or ''CLV''). In this way both mechanisms give rise to a [[feedback loop]], which along with other elements lend a great deal of robustness to the system.<ref name="Brand 2000">{{cite journal |doi=10.1126/science.289.5479.617 |title=Dependence of Stem Cell Fate in Arabidopsis on a Feedback Loop Regulated by CLV3 Activity |year=2000 |last1=Brand |first1=U. |journal=Science |volume=289 |issue=5479 |pages=617–9 |pmid=10915624 |last2=Fletcher |first2=JC |last3=Hobe |first3=M |last4=Meyerowitz |first4=EM |last5=Simon |first5=R|bibcode = 2000Sci...289..617B }}</ref> Along with the ''WUS'' gene the ''SHOOTMERISTEMLESS'' (''STM'') gene also represses the differentiation of the meristematic dome. This gene acts by inhibiting the possible [[cellular differentiation|differentiation]] of the stem cells but still allows [[cell division]] in the daughter cells, which, had they been allowed to differentiate, would have given rise to distinct organs.<ref>{{cite journal |first1=Michael |last1=Lenhard |first2=Gerd |last2=Jürgens |first3=Thomas |last3=Laux |pmid=12070094 |url=http://dev.biologists.org/cgi/pmidlookup?view=long&pmid=12070094 |year=2002 |title=The WUSCHEL and SHOOTMERISTEMLESS genes fulfil complementary roles in Arabidopsis shoot meristem regulation |volume=129 |issue=13 |pages=3195–206 |journal=Development|doi=10.1242/dev.129.13.3195 |url-access=subscription }}</ref>

==Floral architecture==
[[Image:Mature flower diagram.svg|thumb|upright=1.5|Anatomy of a flower]]

A flower's anatomy, as defined by the presence of a series of organs (sepals, petals, stamens and carpels) positioned according to a given pattern, facilitate [[sexual reproduction]] in [[flowering plant]]s. The flower arises from the activity of three classes of genes, which regulate floral development:<ref name="taiz" />
* '''Meristem identity genes''', which code for the [[transcription factor]]s required to initiate the induction of the identity genes. They are positive regulators of organ identity during floral development.
* '''Organ identity genes''', which directly control organ identity and also code for transcription factors that control the expression of other genes, whose products are implicated in the formation or function of the distinct organs of the flower.
* '''Cadastral genes''', which act as spatial regulators for the organ identity genes by defining boundaries for their expression. In this way they control the extent to which genes interact thereby regulating whether they act in the same place at the same time.

===The ABC model===

The ABC model of flower development was first formulated by George Haughn and Chris Somerville in 1988.<ref>{{cite journal |doi=10.1002/dvg.1020090202 |title=Genetic control of morphogenesis in Arabidopsis |year=1988 |last1=Haughn |first1=George W. |last2=Somerville |first2=Chris R. |journal=Developmental Genetics |volume=9 |issue=2 |pages=73–89}}</ref> It was first used as a model to describe the collection of genetic mechanisms that establish floral organ identity in the [[Rosids]], as exemplified by ''Arabidopsis thaliana'', and the [[Asterids]], as demonstrated by ''Antirrhinum majus''. Both species have four verticils (sepals, petals, stamens and carpels), which are defined by the differential expression of a number of [[homeotic gene]]s present in each verticil. This means that the sepals are solely characterized by the expression of A genes, while the petals are characterized by the co-expression of A and B genes. The B and C genes establish the identity of the stamens and the carpels only require C genes to be active. Type A and C genes are reciprocally antagonistic.<ref name="Bowman">{{cite journal |doi=10.1105/tpc.3.8.749 |jstor=3869269 |title=Expression of the Arabidopsis floral homeotic gene AGAMOUS is restricted to specific cell types late in flower development |pmid=1726485 |pmc=160042 |volume=3 |issue=8 |date=August 1991 |pages=749–58 |journal=Plant Cell | last1 = Bowman | first1 = JL | last2 = Drews | first2 = GN | last3 = Meyerowitz | first3 = EM}}</ref>

The fact that these homeotic genes determine an organ's identity becomes evident when a gene that represents a particular function, for example the A gene, is not expressed. In ''Arabidopsis'' this loss results in a flower which is composed of one verticil of carpels, another containing stamens and another of carpels.<ref name="Bowman" /> This method for studying gene function uses [[reverse genetics]] techniques to produce transgenic plants that contain a mechanism for [[gene silencing]] through [[RNA interference]]. In other studies, using [[forward genetics]] techniques such as [[genetic mapping]], it is the analysis of the [[phenotype]]s of flowers with structural anomalies that leads to the [[cloning]] of the gene of interest. The flowers may possess a non-functional or [[gene expression|over expressed]] [[allele]] for the gene being studied.<ref>{{cite journal |doi=10.1126/science.285.5426.380 |title=Plant Functional Genomics |year=1999 |last1=Somerville |first1=C. |journal=Science |volume=285 |issue=5426 |pages=380–3 |pmid=10411495 |last2=Somerville |first2=S|url=http://www.ipef.br/melhoramento/genoma/pdfs/somerville99.pdf }}</ref>

The existence of two supplementary functions, D and E, have also been proposed in addition to the A, B and C functions already discussed. Function D specifies the identity of the [[ovule]], as a separate reproductive function from the development of the carpels, which occurs after their determination.<ref name="Angenent">{{cite journal |pmid=8535139 |doi=10.1105/tpc.7.11.1859 |year=1995 |last1=Colombo |first1=L |last2=Franken |first2=J |last3=Koetje |first3=E |last4=Van Went |first4=J |last5=Dons |first5=HJ |last6=Angenent |first6=GC |last7=Van Tunen |first7=AJ |title=The petunia MADS box gene FBP11 determines ovule identity |volume=7 |issue=11 |pages=1859–68 |pmc=161044 |journal=The Plant Cell}}</ref> Function E relates to a physiological requirement that is a characteristic of all floral verticils, although, it was initially described as necessary for the development of the three innermost verticils (Function E ''sensu stricto'').<ref name="pelaz">{{cite journal |doi=10.1038/35012103 |title=B and C floral organ identity functions require SEPALLATA MADS-box genes |year=2000 |last1=Pelaz |first1=Soraya |last2=Ditta |first2=Gary S. |last3=Baumann |first3=Elvira |last4=Wisman |first4=Ellen |last5=Yanofsky |first5=Martin F. |journal=Nature |volume=405 |issue=6783 |pages=200–3 |pmid=10821278|bibcode=2000Natur.405..200P |s2cid=4391070 }}</ref> However, its broader definition (''sensu lato'') suggests that it is required in the four verticils.<ref name="ditta">{{cite journal |doi=10.1016/j.cub.2004.10.028 |title=The SEP4 Gene of Arabidopsis thaliana Functions in Floral Organ and Meristem Identity |year=2004 |last1=Ditta |first1=Gary |last2=Pinyopich |first2=Anusak |last3=Robles |first3=Pedro |last4=Pelaz |first4=Soraya |last5=Yanofsky |first5=Martin F. |journal=Current Biology |volume=14 |issue=21 |pages=1935–40 |pmid=15530395|s2cid=8122306 |doi-access=free }}</ref> Therefore, when Function D is lost the structure of the ovules becomes similar to that of leaves and when Function E is lost ''sensu stricto'', the floral organs of the three outer most verticils are transformed into sepals,<ref name="pelaz" /> while on losing Function E ''sensu lato'', all the verticils are similar to leaves.<ref name="ditta" /> The [[gene product]]s of genes with D and E functions are also MADS-box genes.<ref name="Ma (2005)">{{cite journal |doi=10.1146/annurev.arplant.55.031903.141717 |title=Molecular Genetic Analyses of Microsporogenesis and Microgametogenesis in Flowering Plants |year=2005 |last1=Ma |first1=Hong |journal=Annual Review of Plant Biology |volume=56 |pages=393–434 |pmid=15862102}}</ref>

===Genetic analysis===
[[Image:Arabidopsis thaliana-flower.jpg|thumb|Flower of ''A. thaliana''.]]
[[Image:Antirrhinum majus6.jpg|thumb|Flowers of ''A. majus''.]]
[[Image:Petunia x hybrida a1.JPG|thumb|Flowers of ''Petunia hybrid''.]]
The methodology for studying flower development involves two steps. Firstly, the identification of the exact genes required for determining the identity of the floral meristem. In ''A. thaliana'' these include APETALA1 (''AP1'') and LEAFY (''LFY''). Secondly, genetic analysis is carried out on the aberrant [[phenotype]]s for the relative characteristics of the flowers, which allows the characterization of the [[homeotic genes]] implicated in the process.{{cn|date=June 2025}}

====Analysis of mutants====
There are a great many [[mutation]]s that affect floral [[morphology (biology)|morphology]], although the analysis of these mutants is a recent development. Supporting evidence for the existence of these mutations comes from the fact that a large number affect the identity of floral organs. For example, some organs develop in a location where others should develop. This is called [[homeotic mutation]], which is analogous to [[Hox gene#Genes regulated by Hox proteins|HOX gene mutations]] found in ''[[Drosophila]]''. In ''Arabidopsis'' and ''[[Antirrhinum]]'', the two taxa on which models are based, these mutations always affect adjacent verticils.{{cn|date=June 2025}}
 
This allows the characterization of three classes of mutation, according to which verticils are affected:
* Mutations in type A genes – These mutations affect the calyx and corolla, which are the outermost verticils. In these mutants, such as APETALA2 in ''A. thaliana'', carpels develop instead of sepals and stamen in place of petals. This means that, the verticils of the [[perianth]] are transformed into reproductive verticils.{{cn|date=June 2025}}
* Mutations in type B genes – These mutations affect the corolla and the stamen, which are the intermediate verticils. Two mutations have been found in ''A. thaliana'', APETALA3 and PISTILLATA, which cause development of sepals instead of petals and carpels in the place of stamen.{{cn|date=June 2025}}
* Mutations in type C genes – These mutations affect the reproductive verticils, namely the stamen and the carpels. The ''A. thaliana'' mutant of this type is called AGAMOUS, it possesses a phenotype containing petals instead of stamen and sepals instead of carpels.{{cn|date=June 2025}}
<gallery>
<!--  no image yet for APETALA2  -->
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Image:Arabidopsis mutants.jpg | AGAMOUS mutation resulting in a [[double-flowered]] [[Arabidopsis thaliana|Arabidopsis]]
</gallery>

====Techniques for detecting differential expression====
[[Cloning]] studies have been carried out on [[DNA]] in the genes associated with the affected homeotic functions in the mutants discussed above. These studies used [[serial analysis of gene expression]] throughout floral development to show patterns of tissue expression, which, in general, correspond with the predictions of the ABC model.{{cn|date=June 2025}}

The nature of these genes corresponds to that of [[transcription factors]], which, as expected, have analogous structures to a group of factors contained in [[yeast]]s and [[animal cells]]. This group is called MADS, which is an acronym for the different factors contained in the group. These MADS factors have been detected in all the vegetable species studied, although the involvement of other elements involved in the [[regulation of gene expression]] cannot be discounted.<ref name="taiz">{{cite book|author1=Taiz '' |author2='' Zeiger | title = Plant physiology | year = 2002 | publisher = Sinauer associates| isbn = 978-0-87893-823-0}}{{page needed|date=April 2013}}</ref>

===Genes exhibiting type-A function===
In ''A. thaliana'', function A is mainly represented by two genes ''APETALA1'' (''AP1)'' and ''APETALA2'' (''AP2'')<ref name="Bowman 1989">{{cite journal |doi=10.1105/tpc.1.1.37 |jstor=3869060 |title=Genes Directing Flower Development in Arabidopsis |year=1989 |last1=Bowman |first1=J. L. |journal=The Plant Cell Online |volume=1 |pages=37–52 |pmid=2535466 |pmc=159735 |issue=1}}</ref> ''AP1'' is a MADS-box type gene, while ''AP2'' belongs to the family of genes that contains AP2, which it gives its name to and which consists of [[transcription factors]] that are only found in plants.<ref name="Jofuku 1994">{{cite journal |pmid=0007919989 |jstor=3869820 |doi=10.1105/tpc.6.9.1211 |year=1994 |last1=Jofuku |first1=KD |last2=Den Boer |first2=BG |last3=Van Montagu |first3=M |last4=Okamuro |first4=JK |title=Control of Arabidopsis flower and seed development by the homeotic gene APETALA2 |volume=6 |issue=9 |pages=1211–25 |pmc=160514 |journal=The Plant Cell}}</ref> AP2 has also been shown to complex with the co-repressor TOPLESS (TPL) in developing floral buds to repress the C-class gene ''AGAMOUS'' (''AG'').<ref name="APETALA2">{{cite journal|last1=Krogan|first1=Naden|title=APETALA2 negatively regulates multiple floral organ identity genes in Arabidopsis by recruiting the co-repressor TOPLESS and the histone deacetylase HDA19|journal=Development|date=November 2012|volume=139|issue=22|pages=4180–90|doi=10.1242/dev.085407|pmid=23034631|pmc=3478687}}</ref> However, ''AP2'' is not expressed in the shoot apical meristem (SAM), which contains the latent stem cell population throughout the adult life of ''Arabidopsis'', and so it is speculated that TPL works with some other A-class gene in the SAM to repress ''AG''.<ref name="APETALA2"/>''AP1'' functions as a type A gene, both in controlling the identity of sepals and petals, and it also acts in the [[floral meristem]]. ''AP2'' not only functions in the first two verticils, but also in the remaining two, in developing ovules and even in leaves. It is also likely that [[post-transcriptional regulation]] exists, which controls its A function, or even that it has other purposes in the determination of organ identity independent of that mentioned here.<ref name="Jofuku 1994" />

In ''Antirrhinum'', the [[homology (biology)|orthologous gene]] to ''AP1'' is ''SQUAMOSA'' (''SQUA''), which also has a particular impact on the floral meristem. The homologs for ''AP2'' are ''LIPLESS1'' (''LIP1'') and ''LIPLESS2'' (''LIP2''), which have a redundant function and are of special interest in the development of sepals, petals and ovules.<ref name="Keck 2003">{{cite journal |doi=10.1093/emboj/cdg097 |title=Separation of genetic functions controlling organ identity in flowers |year=2003 |last1=Keck |first1=Emma |last2=McSteen |first2=Paula |author-link2=Paula McSteen|last3=Carpenter |first3=Rosemary |author-link3=Rosemary Carpenter|last4=Coen |first4=Enrico |journal=The EMBO Journal |volume=22 |issue=5 |pages=1058–66 |pmid=12606571 |pmc=150331}}</ref>

A total of three genes have been isolated from ''Petunia hybrida'' that are similar to ''AP2'': ''P. hybrida APETALA2A'' (''PhAP2A''), ''PhAP2B'' and ''PhAP2C''. ''PhAP2A'' is, to a large degree, homologous with the ''AP2'' gene of ''Arabidopsis'', both in its sequence and in its expression pattern, which suggests that the two genes are orthologs. The proteins ''PhAP2B'' and ''PhAP2C'', on the other hand, are slightly different, even though they belong to the family of transcription factors that are similar to ''AP2''. In addition they are expressed in different ways, although they are very similar in comparison with ''PhAP2A''. In fact, the mutants for these genes do not show the usual phenotype, that of the [[null alleles]] of A genes.<ref name="Maes 2001">{{cite journal |pmid=11226182 |jstor=3871273 |year=2001 |last1=Maes |first1=T |last2=Van De Steene |first2=N |last3=Zethof |first3=J |last4=Karimi |first4=M |last5=d'Hauw |first5=M |last6=Mares |first6=G |last7=Van Montagu |first7=M |last8=Gerats |first8=T |title=Petunia Ap2-like genes and their role in flower and seed development |volume=13 |issue=2 |pages=229–44 |pmc=102239 |journal=The Plant Cell |doi=10.1105/tpc.13.2.229}}</ref> A true A-function gene has not been found in Petunia; though a part of the A-function (the inhibition of the C in the outer two whorls) has been largely attributed to miRNA169 (colloquially called BLIND){{cn|date=June 2025}}

===Genes exhibiting type-B function===
In ''A. thaliana'' the type-B function mainly arises from two genes, ''APETALA3'' (''AP3'') and ''PISTILLATA'' (''PI''), both of which are MADS-box genes. A mutation of either of these genes causes the homeotic conversion of petals into sepals and of stamens into carpels.<ref name=autogenerated1>{{cite journal |pmid=2535466 |jstor=3869060 |year=1989 |last1=Bowman |first1=JL |last2=Smyth |first2=DR |last3=Meyerowitz |first3=EM |title=Genes directing flower development in Arabidopsis |volume=1 |issue=1 |pages=37–52 |doi=10.1105/tpc.1.1.37 |pmc=159735 |journal=The Plant Cell}}</ref> This also occurs in its orthologs in ''A. majus'', which are {{anchor|DEFICIENS}}DEFICIENS (''DEF'') and ''GLOBOSA'' (''GLO'') respectively.<ref name="Sommer 1990">{{cite journal |pmid=1968830 |year=1990 |last1=Sommer |first1=H |last2=Beltrán |first2=JP |last3=Huijser |first3=P |last4=Pape |first4=H |last5=Lönnig |first5=WE |last6=Saedler |first6=H |last7=Schwarz-Sommer |first7=Z |title=Deficiens, a homeotic gene involved in the control of flower morphogenesis in Antirrhinum majus: The protein shows homology to transcription factors |volume=9 |issue=3 |pages=605–13 |pmc=551713 |journal=The EMBO Journal|doi=10.1002/j.1460-2075.1990.tb08152.x }}</ref> For both species the active form of binding with DNA is that derived from the heterodimer: AP3 and PI, or DEF and GLO, [[dimer (chemistry)|dimerize]]. This is the form in which they are able to function.<ref name="Riechmann 1996">{{cite journal |bibcode=1996PNAS...93.4793R |jstor=38855 |title=Dimerization Specificity of Arabidopsis MADS Domain Homeotic Proteins APETALA1, APETALA3, PISTILLATA, and AGAMOUS |last1=Riechmann |first1=Jose Luis |last2=Allyn Krizek |first2=Beth |last3=Meyerowitz |first3=Elliot M. |volume=93 |year=1996 |pages=4793–8 |journal=Proceedings of the National Academy of Sciences of the United States of America |doi=10.1073/pnas.93.10.4793 |pmid=8643482 |issue=10 |pmc=39358|doi-access=free }}</ref>

The ''GLO''/''PI'' lines that have been duplicated in ''Petunia'' contain ''P. hybrida GLOBOSA1'' (''PhGLO1'', also called ''FBP1'') and also ''PhGLO2'' (also called ''PMADS2'' or ''FBP3''). For the functional elements equivalent to ''AP3''/''DEF'' in ''Petunia'' there is both a gene that possesses a relatively similar sequence, called ''PhDEF'' and there is also an atypical B function gene called PhTM6. [[Phylogenetic]] studies have placed the first three within the «euAP3» lineage, while PhTM6 belongs to that of «paleoAP3».<ref>{{cite journal |pmid=14973163 |jstor=3872212 |doi=10.1105/tpc.019166 |year=2004 |last1=Vandenbussche |first1=M |last2=Zethof |first2=J |last3=Royaert |first3=S |last4=Weterings |first4=K |last5=Gerats |first5=T |title=The duplicated B-class heterodimer model: Whorl-specific effects and complex genetic interactions in Petunia hybrida flower development |volume=16 |issue=3 |pages=741–54 |pmc=385285 |journal=The Plant Cell}}</ref> It is worth pointing out that, in terms of evolutionary history, the appearance of the euAP3 line seems to be related with the emergence of [[dicotyledon]]s, as representatives of euAP3-type B function genes are present in dicotyledons while paleoAP3 genes are present in monocotyledons and basal angiosperms, among others.<ref>{{cite journal |pmid=9611190 |url=http://www.genetics.org/cgi/pmidlookup?view=long&pmid=9611190 |year=1998 |last1=Kramer |first1=EM |last2=Dorit |first2=RL |last3=Irish |first3=VF |title=Molecular evolution of genes controlling petal and stamen development: Duplication and divergence within the APETALA3 and PISTILLATA MADS-box gene lineages |volume=149 |issue=2 |pages=765–83 |pmc=1460198 |journal=Genetics|doi = 10.1093/genetics/149.2.765}}</ref>

As discussed above, the floral organs of eudicotyledonous angiosperms are arranged in 4 different verticils, containing the sepals, petals, stamen and carpels. The ABC model states that the identity of these organs is determined by the homeotic genes A, A+B, B+C and C, respectively. In contrast with the sepal and petal verticils of the eudicots, the perigone of many plants of the family [[Liliaceae]] have two nearly identical external petaloid verticils (the [[tepal]]s). In order to explain the floral morphology of the Liliaceae, van Tunen ''et al.'' proposed a modified ABC model in 1993. This model suggests that class B genes are not only expressed in verticils 2 and 3, but also in 1. It therefore follows that the organs of verticils 1 and 2 express class A and B genes and this is how they have a petaloid structure. This theoretical model has been experimentally proven through the cloning and characterization of homologs of the ''Antirrhinum'' genes ''GLOBOSA'' and ''DEFICIENS'' in a Liliaceae, the [[tulip]] ''Tulipa gesneriana''. These genes are expressed in verticils 1,2 and 3.<ref name="Akira Kanno">{{cite journal |doi=10.1023/A:1025070827979 |year=2003 |last1=Kanno |first1=Akira |last2=Saeki |first2=Hiroshi |last3=Kameya |first3=Toshiaki |last4=Saedler |first4=Heinz |last5=Theissen |first5=Günter |journal=Plant Molecular Biology |volume=52 |issue=4 |pages=831–41 |pmid=13677470 |title=Heterotopic expression of class B floral homeotic genes supports a modified ABC model for tulip (Tulipa gesneriana)|s2cid=24366077 }}</ref>
The homologs ''GLOBOSA'' and ''DEFICIENS'' have also been isolated and characterized in ''Agapanthus praecox'' ssp. ''orientalis'' ([[Agapanthaceae]]), which is phylogenetically distant from the model organisms. In this study the genes were called ''ApGLO'' and ''ApDEF'', respectively. Both contain [[open reading frame]]s that code for proteins with 210 to 214 [[amino acid]]s. Phylogenetic analysis of these sequences indicated that they belong to B gene family of the [[monocotyledon]]s. [[In situ hybridization]] studies revealed that both sequences are expressed in verticil 1 as well as in 2 and 3. When taken together, these observations show that the floral development mechanism of ''[[Agapanthus]]'' also follows the modified ABC model.<ref name="Toru Nakamura">{{cite journal |doi=10.1007/s11103-005-5218-z |title=The modified ABC model explains the development of the petaloid perianth of Agapanthus praecox ssp. Orientalis (Agapanthaceae) flowers |year=2005 |last1=Nakamura |first1=Toru |last2=Fukuda |first2=Tatsuya |last3=Nakano |first3=Masaru |last4=Hasebe |first4=Mitsuyasu |last5=Kameya |first5=Toshiaki |last6=Kanno |first6=Akira |journal=Plant Molecular Biology |volume=58 |issue=3 |pages=435–45 |pmid=16021405|s2cid=28657835 }}</ref>

===Genes exhibiting type-C function===
In ''A. thaliana'', the C function is derived from one MADS-box type gene called ''AGAMOUS'' (''AG''), which intervenes both in the establishment of stamen and carpel identity as well as in the determination of the floral meristem.<ref name="Bowman 1989" /> Therefore, the ''AG'' mutants are devoid of [[androecium]] and [[gynoecium]] and they have petals and sepals in their place. In addition, the growth in the centre of the flower is undifferentiated, therefore the petals and sepals grow in repetitive verticils.{{cn|date=June 2025}}

The ''PLENA'' (''PLE'') gene is present in ''A. majus'', in place of the ''AG'' gene, although it is not an ortholog. However, the ''FARINELLI'' (''FAR'') gene is an ortholog, which is specific to the development of the [[anther]]s and the maturation of [[pollen]].<ref name="brendan 1999">{{cite journal |doi=10.1093/emboj/18.14.4023 |title=PLENA and FARINELLI: Redundancy and regulatory interactions between two Antirrhinum MADS-box factors controlling flower development |year=1999 |last1=Davies |first1=Brendan |last2=Motte |first2=Patrick |last3=Keck |first3=Emma |last4=Saedler |first4=Heinz |last5=Sommer |first5=Hans |last6=Schwarz-Sommer |first6=Zsuzsanna |journal=The EMBO Journal |volume=18 |issue=14 |pages=4023–34 |pmid=10406807 |pmc=1171478}}</ref>

In ''Petunia'', ''Antirrhinum'' and in [[maize]] the C function is controlled by a number of genes that act in the same manner. The genes that are closer homologs of ''AG'' in ''Petunia'' are ''pMADS3'' and ''floral-binding protein 6'' (''FBP6'').<ref name="brendan 1999" />

===Genes exhibiting type-D and E functions===
The D function genes were discovered in 1995. These genes are MADS-box proteins and they have a function that is distinct from those previously described, although they have a certain homology with C function genes. These genes are called ''FLORAL BINDING PROTEIN7'' (''FBP7'') and ''FLORAL BINDING PROTEIN1L'' (''FBP1l'').<ref name="Angenent" /> It was found that, in ''Petunia'', they are involved in the development of the ovule. Equivalent genes were later found in ''Arabidopsis'',<ref name="Favaro">{{cite journal |pmid=14555696 |jstor=3872057 |year=2003 |last1=Favaro |first1=R |last2=Pinyopich |first2=A |last3=Battaglia |first3=R |last4=Kooiker |first4=M |last5=Borghi |first5=L |last6=Ditta |first6=G |last7=Yanofsky |first7=MF |last8=Kater |first8=MM |last9=Colombo |first9=L |title=MADS-box protein complexes control carpel and ovule development in Arabidopsis |volume=15 |issue=11 |pages=2603–11 |doi=10.1105/tpc.015123 |pmc=280564 |journal=The Plant Cell}}</ref> where they are also involved in controlling the development of carpels and the ovule and even with structures related to [[seed dispersal]].

The appearance of interesting phenotypes in [[RNA interference]] studies in ''Petunia'' and [[tomato]] led, in 1994, to the definition of a new type of function in the floral development model. The E function was initially thought to be only involved in the development of the three innermost verticils, however, subsequent work found that its expression was required in all the floral verticils.<ref name="pelaz" />

==See also==
* [[Flower]]
* [[MADS-box]]
* [[Mutation]]
* [[Plant evolutionary developmental biology]]
* [[Superman (gene)]]

==References==
{{reflist|30em}}

==Sources==

===General texts===
* {{cite book| editor1-last=Soltis | editor1-first=DE | editor2-last=Soltis | editor2-first=PS | editor2-link = Pamela S. Soltis|editor3-last=Leebens-Mack | editor3-first=J | title = Advances in botanical research: Developmental genetics of the flower | year = 2006 | publisher = New York, NY: Academic Press | isbn = 978-0-12-005944-7}}
* {{cite book | last1 = Wolpert | first1 = Lewis | last2= Beddington | first2=R.| last3= Jessell | first3=T.| last4=Lawrence | first4=P.| last5= Meyerowitz | first5=E. | last6=Smith | first6=W. | title = Principles of Development | edition = Second | year = 2002 | publisher = Oxford University Press | location = Oxford | isbn = 978-0-19-879291-8}}

==External links==
* {{cite journal |author=Murai, K. |year=2013 |title=Homeotic Genes and the ABCDE Model for Floral Organ Formation in Wheat |journal=Plants |volume=2 |issue=3 |pages=379–395 |doi=10.3390/plants2030379|pmid=27137382 |pmc=4844379 |doi-access=free }}

{{botany}}

[[Category:Developmental genetics]]
[[Category:Plant development]]