| K2 | |
| Map: | Haplogroup K of Ydna haplotree.png |
| Origin-Date: | 47,000-50,000 years BP[1] |
| Origin-Place: | Southeast Asia[2] |
| Descendants: | K2a (M2308); K2b (MPS); K2c; K2d; K2e. |
| Mutations: | rs2033003 (M526) |
Haplogroup K2, also known as K-M526 and formerly known as K(xLT) and MNOPS,[3] is a human Y-DNA haplogroup.
Relative to its age, the internal structure of K2 is extremely complex, and subclades of it are carried by males native to regions including Australasia, Oceania, Southeast Asia, South Asia, East Asia, Central Asia, the Americas, Europe, and the Horn of Africa. Many of its branches are very common, the most numerically important being R in Europe and South Asia and O in East and Southeast Asia (as well as recent immigrants to other continents). Haplogroups N and Q, while they are less common overall, are also very widespread, in northern Eurasia and the Americas respectively. M and S are almost entirely restricted to Oceania and eastern Indonesia, where they occur at high frequency. Rare subclades outside of these major lineages are known mainly from Island Southeast Asia (including the Andaman Islands and the Philippines).
Basal paragroup K2* has been identified among native Australians, about 27% of them carry basal K-M526∗.[4]
K2a* has been found only in Upper Paleolithic remains from western Siberia and the Balkans, known respectively as "Ust'-Ishim man" and "Oase-1". The only primary branch of K2a, known as K-M2313*, has been documented in two living individuals, who have ethnic ties to South Asia and South East Asia respectively: a Telugu from India and an ethnic Malay from Singapore. In addition, K-Y28299, which appears to be a primary branch of K-M2313, has been found in three living individuals from India. Another subclade, NO (M214)* – which for a time was thought to be synonymous with K2a (M2308)* – has not been identified in living individuals or remains.
Basal paragroup K2b* has not been identified among living males but was found in Upper Paleolithic Tianyuan man from China.[5] K2b1 (P397/P399) known previously as Haplogroup MS, and Haplogroup P (P-P295), also known as K2b2 are the only primary clades of K2b.
According to geneticist Spencer Wells, haplogroup K, from which haplogroup P descend, originated in the Middle East or Central Asia. It is likely that haplogroup P diverged somewhere in South Asia into P1, which expanded into Siberia and Northern Eurasia, and into P2, which expanded into Oceania and Southeast Asia.[6]
Population geneticist Tatiana Karafet and other researchers (2014) point out that both K2b1 and P* are virtually restricted geographically to South East Asia and Oceania. Whereas, in a striking contrast, P1 (P-M45) and its primary subclades Q and R now make up "the most frequent haplogroup in Europe, the Americas, and Central Asia and South Asia". According to Karafet et al., the estimated dates for the branching of K, K2, K2b and P point to a "rapid diversification" within K2 "that likely occurred in Southeast Asia", with subsequent "westward expansions" of P*, P1, Q and R. However, these authors also stipulated that haplogroup K might have arisen in Eurasia and later went extinct there, and that either origin hypothesis is "equally parsimonious".
A direct descendant of Haplogroup K, K2 is a sibling of basal/paragroup K* and Haplogroup LT (also known as K1). As of 2017, the phylogeny of haplogroup K2 is as follows:
K-M526 (K2) M526 – formerly known as K(xLT) and MNOPS
At the level of highly derived subclades, K2 is almost universal in some modern Eurasian, Australasian and Native American populations. Haplogroup NO (M214), as a descendant of K2a (M2308), includes most males among Southeast Asian, East Asian, and Finno-Ugric-speaking populations.[7] Similarly, the direct descendants of K2b include the major haplogroups M; S, P, Q, and R. These are now numerically in dominant in: Oceania, Central Asia, Siberia, among Native American populations, Europe, and South Asia.
A rapid diversification within and from K2 (M526), most likely in Southeast Asia, is suggested by estimates of the point in time that K2 branched off from K* (M9). Likewise the branching from K2 of K2b (P331) and Haplogroup P (K2b2 P295) from K2b, as well as Haplogroups Q and R from P (K2b2), and their subsequent expansions westward in Europe, and eastward into the Americas.
K2c, K2d, and K2e are extremely rare subhaplogroups that are found in specific parts of South and Southeast Asia.[10] K2c (P261) has been reported only among males in Bali and K2d (P402) only in Java. K2e (M147), which has been found in two modern cases from South India,[10] was provisionally named "pre-NO" (among other names), as it was believed initially to be ancestral to K2a (NO). However, it was later found to be a primary branch of Haplogroup K2 (K-M526) and a sibling of K2a; the new clade was renamed K2e.
Studies published in 2014 and 2015 found that up to 27% of Aboriginal Australian males carry K-M526*, which could not be classified into a known subclade at the time, and another 27% probably have K2b1a1 (P60, P304, P308; also known as "S-P308") and perhaps 2.0% have Haplogroup M1 – also known as M-M4 (or "M-M186") and K2b1d1.[11] [10]
The name K2 was introduced in 2014, following dissatisfaction with the previous names.
K(xLT), the name introduced by the Y Chromosome Consortium in 2012 to replace MNOPS, was controversial. Under the previous methodology, a term such as "K(xLT)" designated all clades and subclades that belonged to K, but did not belong to Haplogroup LT; the haplogroups subordinate to MNOPS would likely have been renamed "U", "V", "W" and "X", and MNOPS would therefore have become "MNOPSUVWX". This posed a problem, because there was no way to disambiguate between "K(xLT)" in the broad and narrow meanings of the term.