Haplogroup BT

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Haplogroup BT M91, also known as Haplogroup A1b2 (and formerly as A4, BR and BCDEF), is a Y-chromosome haplogroup. BT is a subclade of haplogroup A1b (P108) and a sibling of the haplogroup A1b1 (L419/PF712).[1]

Ancient DNA

Later Stone Age individuals excavated at Fingira Rock, Malawi, dated to around 6100 years ago (2/2 males), and at Mount Hora, Malawi, dated to around 8000 years ago (1/1 males), all belonged to Y haplogroup BT(xCT).[2]Template:Efn

Distribution

Basal BT* has not been documented in any living individuals or ancient remains. No definite examples of BT(xCF,DE) – i.e. members of BT outside the only two known branches of CT, namely haplogroups CF and DE – have been identified. In some cases, because testing is undertaken only for geographically and historically likely haplogroups, the data required to identify a precise subclade has not been collected and/or recorded. For instance, research published in 2013, regarding a sample of more than 2,000 men from different parts of Africa, included 7.5% belonging to haplogroup BT(xDE,K).[3] These approximately 150 individuals may have included, for example: B*, unknown primary branches of haplogroups B, BT, CT or CF; haplogroup C, and/or; F(xK) (i.e. haplogroup F* plus its subclades G, H and IJ, but specifically excluding the broader haplogroup K and its subclades, such as haplogroups K*, LT, K2b*, MS, NO, P, Q and R).

Phylogenetics

The ISOGG tree since 2014 has treated M91 as the defining mutation of BT.[4]

  • B M60, M181, P85, P90
  • CT P9.1, M168, M294

Prior to 2002, there were in academic literature at least seven naming systems for the Y-Chromosome Phylogenetic tree. This led to considerable confusion. In 2002, the major research groups came together and formed the Y-Chromosome Consortium (YCC). They published a joint paper that created a single new tree that all agreed to use.

File:Haplogroup A tree.png
The revised y-chromosome family tree by Cruciani et al. (2011) compared with the family tree from Karafet et al. (2008). Cruciani et al. (2011) define BT via M91 and P97, and as a consequence, ISOGG has listed BT since February 2012, and treated M91 as defining mutation for BT since 2014.[5]

See also

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Notes

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References

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  1. ↑ Cite error: Script error: No such module "Namespace detect".Script error: No such module "Namespace detect".
  2. ↑ Script error: No such module "Citation/CS1".
  3. ↑ Script error: No such module "Citation/CS1".
  4. ↑ Y-DNA Haplogroup A and its Subclades - 2012 (BT as subclade of A1b-P108) Y-DNA Haplogroup A and its Subclades - 2014 (BT as subclade of A1b-P108); Y-DNA Haplogroup Tree 2015 (BT-M91 listed as subclade of A1a-M31). ISOGG has listed M42 as a mutation characteristic (but not defining) of BT since 2012.
  5. ↑ ISOGG Haplogroup A (2012): "BT is shown on this tree, though it is not considered to be a part of Haplogroup A, in order to make it clear that, as a sibling clade of A1b1, BT and all other haplogroups are downstream of A1b. Listed 15 February 2012." (also note that the group labelled "A1b" in the image is the "A0" of ISOGG (2012)).

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"Y-chromosomal Adam"
A00 A0-T [χ 1]
A0 A1 [χ 2]
A1a A1b
A1b1 BT
B CT
DE CF
D E C F
F1  F-Y27277 [χ 3]  F3  GHIJK
G HIJK
IJK H
IJ K
I   J     LT [χ 4]       K2 [χ 5]
I1   I2  J1   J2  L     T  K2e K2d K2c K2b [χ 6]  K2a
K2b1 [χ 7]   P [χ 8] K-M2313 [χ 9]
S [χ 10]  M [χ 11]    P1   NO1
P1c P1b P1a N O
R Q

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