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Haplogroup P (Y-DNA)
Human Y-chromosome DNA haplogroup From Wikipedia, the free encyclopedia
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Haplogroup P also known as P-F5850 or K2b2 is a Y-chromosome DNA haplogroup in human genetics. P-F5850 is a branch of K2b (previously Haplogroup MPS; P331), which is a branch of Haplogroup K2 (K-M526).
The haplogroup K2b splits into K2b1 (haplogroup MS*) and K2b2 (haplogroup P-F580, Y-DNA P*). Basal P* (P-PF5850*) is found in Southeast Asia.[5][6] The primary branches (clades) of P-F580 are P-P295 (P1a, formerly P*) which is found among South and Southeast Asians as well as Oceanians, P-FT292000 (P1b, formerly P3) with unknown distribution, and P-M45 (P1c, formerly P1) commonly found among Siberians and Central Asians.[5][7] P-M45 (P1c) is, in turn, the parent node of Haplogroup Q (Q-M242) and Haplogroup R (R-M207).
The major subclades of Haplogroups P-M45, Q and R now include most males among Europeans, Native Americans, South Asians, North Africans, and Central Asians.
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Origin and dispersal
Karafet et al. 2015 suggests an origin and dispersal of haplogroup P and its ancestral clade K from either South Asia or Southeast Asia as part of the early human dispersal, based on the distribution of subclades now classified as P-P295 (now P1a), and more ancient clades such as K1 and K2. However, Karafet, et al. mentions that this hypothesis is "parsimonious" and K may have alternatively originated elsewhere in Eurasia and later went extinct there.[2][8][9] According to a geneticist Spencer Wells, haplogroup K, from which haplogroup P descended, originated most likely in the Middle East or Central Asia.[10] According to Bergstorm et al (2016), haplogroup K2b1 (Y-haplogroup S/M) found in Indigenous Australians and ancestors of haplogroup R and Q (Y-haplogroup K2b2/root P) split in Southeast Asia near Sahul.[11]
The highest frequency and diversity of haplogroup P clades is observed in Southeast Asia, specifically on the Malay Peninsula and the Philippines.[12][5] To date, the ancestral clade K2b has only been confirmed among the 39,000 year old Tianyuan man.[13]
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Structure
The subclades of Haplogroup P with their defining mutation:[5][7]
Distribution
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P1(xP1c)
Because P1a, formerly P2 (P-B253) was discovered relatively recently, it is not always clear if older studies have screened for it. Therefore, cases of basal P1* (also known as P-P295*; K2b2*; PxM45, B253) reported in literature may include P1a (P2).
P1(xP1c) exists at low to moderate levels among various groups in Island South East Asia, the South West Pacific and East Asia.[2]
P1* (perhaps P1a/P2) is found at its highest rate among members of the Aeta (or Agta), a people indigenous to Luzon who formed from various ancient groups, such as Oceanians and Austronesian peoples from Taiwan.[5] P1 is most common among individuals in Siberia and Central Asia, as well as in Southern Asian at lower frequency.[1][2][9][14]
Root P* (P-PF5850*) was found among a Jehai sample in Malaysia.[15][5] Basal P1* was also found in one historical 19th-century Andaman islander.[16]
P-M45 (P1c)
Derived P1c (P-M45) has been found among the Ancient North Eurasian Yana specimens, which carried around 29–47% ancestry from an East Eurasian source represented by the Tianyuan man.[17][18]
Many modern ethnic groups with high frequencies of P1c, also known as P-M45 and K2b2a, are located in Central Asia and Siberia: 35.4% among Tuvans, 28.3% among Altai-Kizhi (PxQ-M3,R1),[19] and 35% among Nivkh males.
§ May include members of haplogroup R2.
Q
Near universal in the Kets (95%) of Siberia. Very common in pre-modern Native American populations and Selkups, except for the Na-Dene peoples, where it reaches 50-90%. Also common, at 25-50% in Siberian populations such as the Siberian Tatars, Nivkh, Tuvans, Chukchi, Siberian Eskimos, Northern Altaians, and in 70% of Turkmens.
R
The only discovered case of basal R* (i.e. one that does not belong to R1 or R2) is the Mal'ta Boy in the Upper Paleolithic on the upper Angara River in the area west of Lake Baikal in the Irkutsk Oblast, Siberia, Russian Federation.
R1
R2
Haplogroup R2 is most common in South Asia and south Central Asia, as well as diaspora populations, such as the Romanis.
P1a (P-B253, formerly P2)
The Aeta (or Agta) people of Luzon in the Philippines have also provided the only known samples of P1a (P-B253).[5]
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Notes
- The first sample recruited for the study by Bowden, Balaresque, et al., followed the usual sampling strategy: Evidence of two generations of residence in a studied location were sufficient to qualify a donor to participate in the study of DNA localised to a particular geographical area. They contrasted this 'modern' group with a 'medieval' group they recruited, in whom they required additional "cultural markers" of ancestry.
- For a sample with local (either: West Lancashire; or the Wirral) ancestry likely going back to the time of the Viking influx into Northern England, Bowden, Balaresque, et al. used special inclusion criteria:
"Subjects for the second sample ('medieval') were also required to have at least two generations of residence, and to have their earliest recorded patrilineal ancestor born in the relevant area. However, in addition they were required to carry surnames that were present in the relevant region prior to 1572 as judged by documentary sources"
— Bowden, Balaresque, et al. (2008)
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References
External links
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