Haplogroup O-M122

Haplogroup O-M122
Possible time of origin	About 30,000 years ago (Shi 2009)
Possible place of origin	China (GenographicProject 2005) or Southeast Asia (Shi 2009)
Ancestor	O-M175
Defining mutations	M122 (Krahn and FTDNA 2013)

In human population genetics, haplogroups define the major lineages of direct paternal (male) lines back to a shared common ancestor in Africa. Haplogroup O-M122 is an Eastern Eurasian Y-chromosome haplogroup. The lineage has spread from Southeast Asia across East Asia. It dominates the paternal lineages there with extremely high frequencies.

This lineage is a descendant haplogroup of haplogroup O-M175.

Origins

Most researchers believe that O-M122 first appeared in Southeast Asia approximately 25,000-30,000 years ago (Shi 2009). In a systematic sampling and genetic screening of an East Asian–specific Y-chromosome haplogroup (O-M122) in 2,332 individuals from diverse East Asian populations, results indicate that the O-M122 lineage is dominant in East Asian populations, with an average frequency of 44.3%. Microsatellite data show that the O-M122 haplotypes are more diverse in Southeast Asia than those in northern East Asia (Shi 2009). This suggests a southern origin of the O-M122 mutation to be likely.

It was also part of the settlement of East Asia. However, the prehistoric peopling of East Asia by modern humans remains controversial with respect to early population migrations and the place of the O-M122 lineage in these migrations is ambivalent.

Distribution

Although Haplogroup O-M122 appears to be primarily associated with Chinese people, it also forms a significant component of the Y-chromosome diversity of most modern populations of the East Asian region.

Population	Frequency	Count	Source	SNPs
Derung	1		Shi 2009
Nishi	0.94		Cordaux 2004
Adi	0.89		Cordaux 2004
Tamang	0.867	45	Gayden 2007	M134
Nu	0.86		Wen 2004
Yao	0.83		Xue 2005
Achang	0.825		Shi 2009
Apatani	0.82		Cordaux 2004
Bai	0.82		Shi 2009
Naga	0.76		Cordaux 2004
Ava (Yunnan)	0.759	29	Cai 2011	M122
Han Chinese	0.74		Wen 2004c
She	0.74		Xue 2005
Nu	0.7		Shi 2009
Miao	0.7		Karafet 2001
Shui	0.7		Shi 2009
Lisu	0.65		Wen 2004
Zaomin (Guangdong)	0.649	37	Cai 2011	M122
She	0.63		Karafet 2001
Filipinos	0.62		Jin 2009
Taiwan Han	0.619	21	Tajima 2004	M122
Philippines	0.607	28	Hurles 2005	M122
Han (East China)	0.593	167	Yan 2011	M122
Garo	0.59		Reddy 2007
Han (North China)	0.566	129	Yan 2011	M122
Toba (Sumatra)	0.553	38	Karafet 2010	P201(xM7, M134)
Northern Han	0.551	49	Tajima 2004	M122
Garo	0.55		Kumar 2007
Tujia	0.54		Shi 2009
Tujia	0.53		Karafet 2001
Han (South China)	0.492	65	Yan 2011	M122
Va	0.48		Shi 2009
Bai	0.48		Shi 2009 and Wen 2004
Lisu	0.47		Shi 2009
Hani	0.47		Wen 2004
Bai (Dali, Yunnan)	0.46	50	Wen 2004	M122
Manchu	0.45		Katoh 2004
Koreans	0.443	506	Kim 2011	O-P201=146 O-M324(xP201)=76 O-M122(xM324)=2
Tibetans (Zhongdian, Yunnan)	0.44	50	Wen 2004	M122
Miao	0.44		Shi 2009
Hezhe	0.44		Xue 2005
Yi	0.44		Wen 2004
Koreans	0.43		Kim 2007
Lahu	0.43		Shi 2009
Bit (Laos)	0.429	28	Cai 2011	M122
Hmong Daw (Laos)	0.412	51	Cai 2011	M122
Vietnamese	0.41		Karafet 2001
Dai	0.4		Yang 2005
Dungan (Kyrgyzstan)	0.40	40	Wells 2001	M122
Vietnamese	0.39		Jin 2009
Blang (Yunnan)	0.385	52	Cai 2011	M122
Manchu	0.38		Karafet 2001
Philippine (Tagalog language group)	0.380	50	Tajima 2004	M122
Lahu	0.36		Wen 2004
Qiang	0.36		Xue 2005
Borneo, Indonesia	0.36	86	Karafet 2010	M122
Korean	0.356	45	Wells 2001	M122
Pahng (Guangxi)	0.355	31	Cai 2011	M122
Philippines	0.354	48	Karafet 2010	M122
Western Yugur	0.35		Zhou 2008
Thai (Chiang Mai and Khon Kaen)	0.353	34	Shi 2009 and Tajima 2004	M122
Tharu	0.345	171	Fornarino 2009	M134
Kinh (Hanoi, Vietnam)	0.342	76	He 2012	M122
Tibet	0.340	156	Gayden 2007	M122
Yao	0.34		Xue 2005
Kazakhs (SE Altai)	0.337	89	Dulik 2011	M134(xM117, P101)
Polynesians	0.325		Su 2000
Tibetans	0.32		Wen 2004
Khasi	0.32		Reddy 2007
Lao (Luang Prabang, Laos)	0.32	25	He 2012	M122
Eastern Yugur	0.31		Zhou 2008
Malays	0.31		Karafet 2001
Buyei	0.31		Xue 2005
Han (Pinghua speakers)	0.3		Gan 2008
Koreans	0.3		Katoh 2004
Salar	0.3		WeiWang 2003
Khasi	0.29		Kumar 2007
Zhuang	0.29		Su 2000
Bonan	0.28		WeiWang 2003
Sibe	0.27		Xue 2005
Micronesia	0.27		Su 2000
Daur	0.26		Xue 2005
Polynesians	0.25		Hammer 2005 and Kayser 2006
Bunu (Guangxi)	0.25	36	Cai 2011	M122
Malay (near Kuala Lumpur)	0.25	12	Tajima 2004	M122
Dongxiang	0.24		WeiWang 2003
Manchurian Evenks	0.24		Karafet 2001
Thai (Northern Thailand)	0.235	17	He 2012	M122
Mosuo (Ninglang, Yunnan)	0.234	47	Wen 2004	M122
Manchurian Evenks	0.23		Xue 2005
Mosuo	0.23		Wen 2004
Mongols	0.23		Hammer 2005
Japanese	0.23		Xue 2005
Khmers	0.22		Black 2006
Mal (Laos)	0.22	50	Cai 2011	M122
Newar	0.212	66	Gayden 2007	M117
Blang	0.21		Shi 2009
Okinawans	0.21		Nonaka 2007
Kathmandu, Nepal	0.208	77	Gayden 2007	M324
Shui	0.2		Xie 2004
Yi (Shuangbai, Yunnan)	0.20	50	Wen 2004	M122(xM7)
Khmu (Laos)	0.196	51	Cai 2011	M122
Hani	0.18		Xue 2005
Micronesia	0.18		Hammer 2005
Mandar (Sulawesi)	0.167	54	Karafet 2010	M122
Okinawans	0.16		Hammer 2005
Thai	0.16		Jin 2009
Zhuang	0.16		Karafet 2001
Japanese	0.16		Katoh 2004
Aheu (Laos)	0.158	38	Cai 2011	M122
Bugan (Yunnan)	0.156	32	Cai 2011	M122
Cambodia	0.14		Shi 2009
Cham (Binh Thuan, Vietnam)	0.136	59	He 2012	M122
Java (mainly sampled in Dieng)	0.131	61	Karafet 2010	M122
Aboriginal Taiwanese	0.126	223	Tajima 2004	M122
Uighur (Kazakhstan)	0.122	41	Wells 2001	M122
Uzbek (Bukhara)	0.121	58	Wells 2001	M122
Karakalpak (Uzbekistan)	0.114	44	Wells 2001	M122
Bo (Laos)	0.107	28	Cai 2011	M122
Tibetans	0.1		Zhou 2008
Maluku Islands	0.1	30	Karafet 2010	M122
Kazakh (Kazakhstan)	0.093	54	Wells 2001	M122
Pumi (Ninglang, Yunnan)	0.085	47	Wen 2004	M122(xM7)
Mongols	0.083	24	Wells 2001	M122
Balinese (Bali)	0.073	641	Karafet 2010	M122
Sinte (Uzbekistan)	0.067	15	Wells 2001	M122
Iranian (Esfahan)	0.063	16	Wells 2001	M122
Flores	0.046	394	Karafet 2010	M122
Buyei	0.04		Yang 2005
Kazakhs (SW Altai)	0.033	30	Dulik 2011	M134(xM117, P101)
Burusho	0.031	97	Firasat 2007	M122
Sumba	0.029	350	Karafet 2010	M122
Naxi (Lijiang, Yunnan)	0.025	40	Wen 2004	M134
Pathan	0.010	96	Firasat 2007	M122
Pakistan	0.005	638	Firasat 2007	M122

Haplogroup O-M122's brother clade, Haplogroup O-MSY2.2, displays a similar geographical distribution, being found among nearly all the populations of East and Southeast Asia, but generally at a frequency much lower than that of Haplogroup O-M122. Another brother clade, Haplogroup O-P31, has an impressive extent of dispersal, as it is found among the males of populations as widely separated as the Kolarians of India and the Japanese of Japan; however, Haplogroup O-P31's distribution is much more patchy, and the Haplogroup O-P31 Y-chromosomes found among the Mundas and the Japanese belong to distinct subclades.

East Asia

Haplogroup O-M122 is found in over 50% of all modern Han Chinese males (with frequency ranging from 30/101=29.7% among Pinghua-speaking Hans in Guangxi (Gan et al. 2008) to 110/148=74.3% among Hans in Changting, Fujian (Wen et al. 2004c)), about 40% of Manchu, Korean, and Vietnamese males, about 33.3% (Hammer et al. 2005) to 62% (Jin et al. 2009 and (Hurles et al. 2005)) of Filipino males, about 10.5% (Su et al. 2000) to 55.6% (Su et al. 2000) of Malaysian males, about 10% (4/39 Guide County, Qinghai) (Zhou et al. 2008) to 45% (22/49 Zhongdian County, Yunnan) (Wen et al. 2004) of Tibetan males, about 20% (10/50 Shuangbai, northern Yunnan) (Wen et al. 2004) to 44% (8/18 Xishuangbanna, southern Yunnan) (Wen et al. 2004) and (Karafet et al. 2001) of Yi males, about 25% of Zhuang (Jing et al. 2006) and Indonesian (HuiLi et al. 2008) males, and about 16% (Katoh et al. 2004) and (Nonaka et al. 2007) to 20% (Hammer et al. 2005) of Japanese males. The distribution of Haplogroup O-M122 stretches far into Asia (approx. 40% of Dungans (Wells et al. 2001), 30% of Salars (WeiWang et al. 2003), 28% of Bonan (WeiWang 2003), 24% of Dongxiang (WeiWang et al. 2003), 18% to 22.8% of Mongolians (Hammer et al. 2005), 12% of Uyghurs (Wells et al. 2001), 9% of Kazakhs (Wells et al. 2001), 6.2% of Altaians (Kharkov et al. 2007), and 4.1% of Uzbeks (Wells et al. 2001).

Southeast Asia

Haplogroup O-M122 is also found very frequently among populations of Northeast India (Garo 42/71=59.2%, (Reddy 2007) Khasi 112/353=31.7% (Reddy 2007)) and Nepal (Tamang 39/45=86.7%, Newar 14/66=21.2%, general population of Kathmandu 16/77=20.8%). (Gayden 2007) Among all the populations of East and Southeast Asia, Haplogroup O-M122 is most closely associated with those that speak a Sinitic, Tibeto-Burman, or Hmong–Mien language. Haplogroup O-M122 comprises about 50% or more of the total Y-chromosome variation among the populations of each of these language families. The Sinitic and Tibeto-Burman language families are generally believed to be derived from a common Sino-Tibetan protolanguage, and most linguists place the homeland of the Sino-Tibetan language family somewhere in northern China. The Hmong–Mien languages and cultures, for various archaeological and ethnohistorical reasons, are also generally believed to have derived from a source somewhere north of their current distribution, perhaps in northern or central China. The Tibetans, however, despite the fact that they speak a language of the Tibeto-Burman language family, have high percentages of the otherwise rare haplogroups D-M15 and D3, which are also found at much lower frequencies among the members of some other ethnic groups in East Asia and Central Asia.

Haplogroup O-M122 has been implicated as a diagnostic genetic marker of the Austronesian expansion when it is found in populations of insular Southeast Asia and Oceania. It appears at moderately high frequencies in the Philippines, Malaysia, and Indonesia. Its distribution in Oceania is mostly limited to the traditionally Austronesian culture zones, chiefly Polynesia (approx. 25% (Hammer 2005) to 32.5% (Su 2000)). O-M122 is found at generally lower frequencies in coastal and island Melanesia, Micronesia, and Taiwanese aboriginal tribes (18% (Hammer 2005) to 27.4% (Su 2000) of Micronesians, and 5% of Melanesians (Karafet 2005), albeit with reduced frequencies of most subclades.

It should be noted that Haplogroup O-M122* Y-chromosomes, which are not defined by any identified downstream markers, are actually more common among certain non-Han Chinese populations than among Han Chinese ones, and the presence of these O-M122* Y-chromosomes among various populations of Central Asia, East Asia, and Oceania is more likely to reflect a very ancient shared ancestry of these populations rather than the result of any historical events. It remains to be seen whether Haplogroup O-M122* Y-chromosomes can be parsed into distinct subclades that display significant geographical or ethnic correlations.

Subclade Distribution

Paragroup O-M122*

Paragroup O3*-M122(xO3a-P197) Y-DNA is quite rare, having been detected only in 2/165 = 1.2% of a sample of Han Chinese in a pool of samples from mainland China, Taiwan, the Philippines, Vietnam, and Malaysia (n=581), 8/641 = 1.2% of a sample of Balinese in a pool of samples from western Indonesia (n=960), and 7/350 = 2.0% of a sample of males from Sumba in a pool of samples from eastern Indonesia (n=957). In the same study, O3*-M122(xO3a-P197) Y-DNA was not observed in a pool of samples from Oceania (n=182) (Karafet 2010).

A paper published by a group of mainly Chinese geneticists in the American Journal of Human Genetics in 2005 reported the detection of O3*-M122(xO3a-M324) Y-DNA in 1.6% (8/488) of a pool of seven samples of Han Chinese (3/64 = 4.7% Sichuan, 2/98 = 2.0% Zibo, Shandong, 1/60 = 1.7% Inner Mongolia, 1/81 = 1.2% Yunnan, 1/86 = 1.2% Laizhou, Shandong, 0/39 Guangxi, 0/60 Gansu). O3*-M122(xO3a-M324) Y-DNA also was detected in the following samples of ethnic minorities in China: 5.9% (1/17) Jingpo from Yunnan, 4.3% (2/47) Zhuang from Yunnan, 4.1% (2/49) Lisu from Yunnan, 3.2% (1/31) Wa from Yunnan, 2.6% (1/39) Zhuang from Guangxi, 2.5% (2/80) Bai from Yunnan, 2.4% (1/41) Hani from Yunnan, 2.3% (2/88) Lahu from Yunnan, 2.1% (1/47) Yi from Yunnan, 2.1% (1/48) Miao from Yunnan, 1.5% (2/132) Dai from Yunnan, 1.0% (1/105) Miao from Hunan, and 0.9% (2/225) Yao from Guangxi.^[1]

O3*-M122(xO3a-M324) Y-DNA has been found as a singleton (1/156 = 0.6%) in a sample from Tibet.(Gayden 2007)

In a paper published in 2011, Korean researchers have reported finding O3*-M122(xO3a-M324) Y-DNA in the following samples: 5.9% (3/51) Beijing Han, 3.1% (2/64) Filipino, 2.1% (1/48) Vietnamese, 1.7% (1/60) Yunnan Han, 0.4% (2/506) Korean.^[2]

In 2011, Chinese researchers published a paper reporting their finding of O3*-M122(xO3a-M324) Y-DNA in 3.0% (5/167) of a sample of Han Chinese with origins in East China (defined as consisting of Jiangsu, Zhejiang, Shanghai, and Anhui) and in 1.5% (1/65) of a sample of Han Chinese with origins in Southern China. O3* Y-DNA was not detected in their sample of Han Chinese with origins in Northern China (n=129).

In a paper published in 2012, O3*-M122(xO3a-P200) Y-DNA was found in 12% (3/25) of a sample of Lao males from Luang Prabang, Laos. O3* Y-DNA was not detected in this study's samples of Cham from Binh Thuan, Vietnam (n=59), Kinh from Hanoi, Vietnam (n=76), or Thai from northern Thailand (n=17).(He 2012)

O-M324

O-M121

O3a1a-M121 is a subclade of O3a1-L127.1, parallel to O3a1b-M164 and O3a1c-JST002611.

In an early survey of Y-DNA variation in present-day human populations of the world, O-M121 was detected only in 5.6% (1/18) of a sample from Cambodia and Laos and in 5.0% (1/20) of a sample from China.^[3]

In a large study of 2,332 unrelated male samples collected from 40 populations in East Asia (and especially Southwest China), O-M121/DYS257 Y-DNA was detected only in 7.1% (1/14) of a sample of Cambodians and in 1.0% (1/98) of a sample of Han Chinese from Zibo, Shandong.^[1]

In a study published in 2011, O-M121 Y-DNA was found in 1.2% (2/167) of a sample of Han Chinese with origins in East China, defined as consisting of Jiangsu, Anhui, Zhejiang, and Shanghai, and in 0.8% (1/129) of a sample of Han Chinese with origins in Northern China. O-M121 was not detected in this study's sample of Han Chinese with origins in Southern China (n=65).(Yan 2011)

O-M164

O3a1b-M164 is a subclade of O3a1-L127.1, parallel to O3a1a-M121 and O3a1c-JST002611.

In an early survey of Y-DNA variation in present-day human populations of the world, O-M164 was detected only in 5.6% (1/18) of a sample from Cambodia and Laos.^[3]

In a large study of 2,332 unrelated male samples collected from 40 populations in East Asia (and especially Southwest China), O3a1b-M164 Y-DNA was detected only in 7.1% (1/14) of a sample of Cambodians.^[1]

O-002611

Haplogroup O3a1c-JST002611 is derived from O3-M122 via O3a-M324/P93/P197/P199/P200 and O3a1-L127.1/L465/L467. O3a1c-JST002611 is the most commonly observed type of O3a1 Y-DNA, and, more generally, represents the majority of extant O3-M122 Y-DNA that does not belong to the expansive subclade O3a2-P201.

Haplogroup O3a1c-JST002611 was first identified in 3.8% (10/263) of a sample of Japanese (Nonaka et al. 2007). Subsequently, this haplogroup has been found with higher frequency in some samples taken in and around China, including 12/58 = 20.7% Miao (China), 10/70 = 14.3% Vietnam, 18/165 = 10.9% Han (China & Taiwan), 4/49 = 8.2% Tujia (China) (Karafet 2010). O-002611 also has been found in a singleton from the Philippines (1/48 = 2.1%), but it has not been detected in samples from Malaysia (0/32), Taiwanese Aboriginals (0/48), She from China (0/51), Yao from China (0/60), Oceania (0/182), eastern Indonesia (0/957), or western Indonesia (0/960) (Karafet 2010).Haplogroup O3a1c‐002611 is prevalent in different ethnic groups in China and Southeast Asia, including Vietnam (14.29%), Sichuan of southwestern China (Han, 14.60%; Tibetan in Xinlong County, 15.22%),^[4] Jilin of northeastern China (Korean, 9.36%), Inner Mongolia(Mongolian, 6.58%), and Gansu of northwestern China(Baima, 7.35%; Han, 11.30%).^[5]

O-P201

O3a2-JST021354/P201 is a subclade of O3a that includes the most common types of O3-M122 Y-DNA. This clade includes the major subclades O3a2c1-M134 (subclade of O-P164) and O3a2b-M7, which exhibit expansive distributions centered on China, as well as an assortment of Y-chromosomes that have not yet been assigned to any subclade.

O3a2-P201(xO3a2b-M7, O3a2c1-M134) Y-DNA has been detected with high frequency in many samples of Austronesian-speaking populations, in particular some samples of Batak Toba from Sumatra (21/38 = 55.3%), Tongans (5/12 = 41.7%), and Filipinos (12/48 = 25.0%). (Karafet 2010) Outside of Austronesia, O3a2-P201(xO3a2b-M7, O3a2c1-M134) Y-DNA has been observed in samples of Tujia (7/49 = 14.3%), Han Chinese (14/165 = 8.5%), Japanese (11/263 = 4.2%), Miao (1/58 = 1.7%), and Vietnam (1/70 = 1.4%) (Karafet 2010 and Nonaka 2007).

O-M159

O3a2a-M159 is a subclade of O3a2-P201. In an early survey of Y-DNA variation in present-day human populations of the world, O-M159 was detected only in 5.0% (1/20) of a sample from China.^[3]

Unlike its phylogenetic siblings, O-M7 and O-M134, O-M159 is very rare, having been found only in 2.9% (1/35) of a sample of Han males from Meixian, Guangdong in a study of 988 males from East Asia.(Xue 2006)

In a study published in 2011, O-M159 was detected in 1.5% (1/65) of a sample of Han Chinese with origins in Southern China. O-M159 was not detected in the same study's samples of Han Chinese with origins in East China (n=167) or Northern China (n=129).(Yan 2011)

O-M7

Haplogroup O3a2b-M7 Y-DNA has been detected with high frequency in some samples of populations who speak Hmong-Mien languages, Katuic languages, or Bahnaric languages, scattered through some mostly mountainous areas of southern China, Laos, and Vietnam (Cai 2010).

O-M7 has been noted for having a widespread but uneven distribution among populations that speak Hmong-Mien languages, such as She (29/51 = 56.9% She, 10/34 = 29.4% She, 14/56 = 25.0% Northern She from Zhejiang), Miao (21/58 = 36.2% Miao from China, 17/51 = 33.3% Hmong Daw from northern Laos, 6/49 = 12.2% Yunnan Miao, 2/49 = 4.1% Guizhou Miao, 4/100 = 4.0% Hunan Miao), and Yao (18/35 = 51.4% Yao from Liannan, Guangdong, 29/60 = 48.3% Yao from Guangxi, 12/35 = 34.3% Yao from Bama, Guangxi, 12/37 = 32.4% Zaomin from Guangdong, 5/36 = 13.9% Bunu from Guangxi, 1/11 = 9.1% Top-Board Mien, 3/41 = 7.3% Native Mien, 2/31 = 6.5% Southern Mien from Guangxi, 1/19 = 5.3% Flowery-Headed Mien from Guangxi, 1/20 = 5.0% Mountain Straggler Mien from Hunan, 1/28 = 3.6% Blue Kimmun from Guangxi, 1/31 = 3.2% Pahng from Guangxi, 1/47 = 2.1% Western Mien from Yunnan, 0/11 Thin Board Mien, 0/31 Lowland Yao from Guangxi, 0/32 Mountain Kimmun from Yunnan, 0/33 Northern Mien, and 0/41 Lowland Kimmun from Guangxi). (Cai 2010)(Karafet 2010)(Xue 2006)

Cai et al. 2010 have reported finding high frequencies of O-M7 in their samples of Katuic (17/35 = 48.6% Ngeq, 10/45 = 22.2% Katu, 6/37 = 16.2% Kataang, 3/34 = 8.8% Inh (Ir), 4/50 = 8.0% So, 1/39 = 2.6% Suy) and Bahnaric (15/32 = 46.9% Jeh, 17/50 = 34.0% Oy, 8/32 = 25.0% Brau, 8/35 = 22.9% Talieng, 4/30 = 13.3% Alak, 6/50 = 12.0% Laven) peoples from southern Laos. Among the sampled Katuic peoples, the speakers of West Katuic (Kuy-Bru), such as the So and the Suy, have lower frequencies of O-M7 than the Katu proper and the speakers of the Ta'Oi dialect chain (Ngeq, Kataang, Ir). However, O-M7 has been found only with low frequency in samples of linguistically related Khmuic populations from northern Laos (1/50 = 2.0% Mal, 1/51 = 2.0% Khmu, 0/28 Bit, 0/29 Xinhmul), Vietic peoples from Vietnam and central Laos (8/76 = 10.5% Kinh from Hanoi, Vietnam, 2/28 = 7.1% Bo, 4/70 = 5.7% Vietnamese, 0/12 Muong, 0/15 Kinh, 0/38 Aheu), Palaungic peoples from northwestern Laos and southwestern Yunnan (2/35 = 5.7% Lamet, 0/29 Ava, 0/52 Blang), and Pakanic peoples from southeastern Yunnan and northwestern Guangxi (0/30 Palyu, 0/32 Bugan).(Cai 2010)(Karafet 2010)(He 2012)

Haplogroup O-M7 has been found with notable frequency in some samples of Austronesian populations from the central part of the Malay Archipelago (17/86 = 19.8% Indonesians from Borneo, 4/32 = 12.5% Malaysia, 7/61 = 11.5% Java (mostly sampled in Dieng)), but the frequency of this haplogroup appears to drop off very quickly toward the east (1/48 = 2.1% Philippines, 5/641 = 0.8% Balinese, 0/48 Taiwanese Aboriginals) and west (0/38 Batak Toba from Sumatra, 0/60 Nias, 0/74 Mentawai). (Karafet 2010) O-M7 has been found in 5.1% (3/59) of a sample of the Austronesian-speaking Cham people from Binh Thuan, Vietnam. (He 2012)

In the northern fringes of its distribution, O-M7 has been found in samples of Oroqen (2/31 = 6.5%), Tujia from Hunan (3/49 = 6.1%), Qiang (2/33 = 6.1%), and Han Chinese (3/165 = 1.8% Han Chinese, or 2/32 = 6.3% Han from Yili, Xinjiang, 4/66 = 6.1% Han from Huize, Yunnan, 2/35 = 5.7% Han from Meixian, Guangdong, 1/18 = 5.6% Han from Wuhan, Hubei, 6/148 = 4.1% Han from Changting, Fujian, 2/63 = 3.2% Han from Weicheng, Sichuan, 2/100 = 2.0% Han from Nanjing, Jiangsu, 1/55 = 1.8% Han from Shanghai).(Wen 2004)(Xue 2006)(Karafet 2010)

O-M134

O-M134*

Paragroup O-M134(xM117) has been found with very high frequency in some samples of Kim Mun people, a subgroup of the Yao people of southern China (16/32 = 50.0% Mountain Kimmun from southern Yunnan, 11/28 = 39.3% Blue Kimmun from western Guangxi). However, this paragroup has been detected in only 3/41 = 7.3% of a sample of Lowland Kimmun from eastern Guangxi (Cai et al. 2011). This paragroup also has been found with high frequency in some Kazakh samples, especially the Naiman tribe(Dulik et al. 2011 and Lu et al. 2011) Dulik hypothesizes that O-M134 in Kazakhs was due to a later expansion due to its much more recent TMRCA time.

The general outline of the distribution of O-M134(xM117) among modern populations is different as that of the related clade O-M117. In particular, O-M134(xM117) occurs with only low frequency or is nonexistent among most Tibeto-Burman-speaking populations of Southwest China, Northeast India, and Nepal, who exhibit extremely high frequencies of O-M117. This paragroup also occurs with very low frequency or is non-existent among most Mon-Khmer population of Laos, who exhibit much higher frequencies of O-M117 (Cai et al. 2011). In Han Chinese, the paragroup is found in approximately the same percentage as O-M117, but has a higher distribution in northern Han Chinese than Southern Han Chinese (Yan et al. 2012).

O-M117

Haplogroup O3a2c1a-M117 (also defined by the phylogenetically equivalent mutations M133 and Page23) is a subclade of O3a2c1-M134 that occurs frequently in China and in neighboring countries, especially among Tibeto-Burman-speaking peoples.

O-M117 has been detected in samples of Tamang (38/45 = 84.4%), Tibetans (45/156 = 28.8% or 13/35 = 37.1%), Tharus (57/171 = 33.3%), Han Taiwanese (40/183 = 21.9%), Newars (14/66 = 21.2%), the general population of Kathmandu, Nepal (13/77 = 16.9%), Han Chinese (5/34 = 14.7% Chengdu, 5/35 = 14.3% Harbin, 4/35 = 11.4% Meixian, 3/30 = 10.0% Lanzhou, 2/32 = 6.3% Yili), Tungusic peoples from the PRC (7/45 = 15.6% Hezhe, 4/26 = 15.4% Ewenki, 5/35 = 14.3% Manchu, 2/41 = 4.9% Xibe, 1/31 = 3.2% Oroqen), Koreans (4/25 = 16.0% Koreans from the PRC, 5/43 = 11.6% Koreans from South Korea), Mongols (5/45 = 11.1% Inner Mongolian, 3/39 = 7.7% Daur, 3/65 = 4.6% Outer Mongolian), and Uyghurs (2/39 = 5.1% Yili, 1/31 = 3.2% Urumqi) (Xue et al. 2006, Gayden et al. 2007, and Fornarino et al. 2009).

Like O-M7, O-M117 has been found with greatly varying frequency in many samples of Hmong-Mien-speaking peoples, such as Mienic peoples (7/20 = 35.0% Mountain Straggler Mien, 9/28 = 32.1% Blue Kimmun, 6/19 = 31.6% Flower Head Mien, 3/11 = 27.3% Top Board Mien, 3/11 = 27.3% Thin Board Mien, 11/47 = 23.4% Western Mien, 6/33 = 18.2% Northern Mien, 5/31 = 16.1% Lowland Yao, 5/35 = 14.3% Yao from Liannan, Guangdong, 5/37 = 13.5% Zaomin, 5/41 = 12.2% Lowland Kimmun, 3/41 = 7.3% Native Mien, 2/31 = 6.5% Southern Mien, 2/32 = 6.3% Mountain Kimmun, but 0/35 Yao from Bama, Guangxi), She (6/34 = 17.6% She, 4/56 = 7.1% Northern She), and Hmongic peoples (9/100 = 9.0% Miao from Hunan, 4/51 = 7.8% Hmong Daw from northern Laos, 3/49 = 6.1% Miao from Yunnan, 1/49 = 2.0% Miao from Guizhou, but 0/36 Bunu from Guangxi) (Cai et al. 2011 and Xue et al. 2006).

In a study published by Chinese researchers in the year 2006, O-M117 was found with high frequency (8/47 = 17.0%) in a sample of Japanese of undescribed geographical origin (Xue et al. 2006). However, in a study published by Japanese researchers in the year 2007, the same haplogroup was found with much lower frequency (11/263 = 4.2%) in a larger sample of Japanese from various regions of Japan (Nonaka et al. 2007).

In Meghalaya, a predominantly tribal state of Northeast India, O-M133 has been found in 19.7% (14/71) of a sample of the Tibeto-Burman-speaking Garos, but in only 6.2% (22/353, ranging from 0/32 Bhoi to 6/44 = 13.6% Pnar) of a pool of eight samples of the neighboring Khasian-speaking tribes (Reddy et al. 2007).

O-M333

Phylogenetics

Phylogenetic History

Main article: Conversion table for Y chromosome haplogroups

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. Later, a group of citizen scientists with an interest in population genetics and genetic genealogy formed a working group to create an amateur tree aiming at being above all timely. The table below brings together all of these works at the point of the landmark 2002 YCC Tree. This allows a researcher reviewing older published literature to quickly move between nomenclatures.

YCC 2002/2008 (Shorthand)	(α)	(β)	(γ)	(δ)	(ε)	(ζ)	(η)	YCC 2002 (Longhand)	YCC 2005 (Longhand)	YCC 2008 (Longhand)	YCC 2010r (Longhand)	ISOGG 2006	ISOGG 2007	ISOGG 2008	ISOGG 2009	ISOGG 2010	ISOGG 2011	ISOGG 2012
O-M175	26	VII	1U	28	Eu16	H9	I	O*	O	O	O	O	O	O	O	O	O	O
O-M119	26	VII	1U	32	Eu16	H9	H	O1*	O1a	O1a	O1a	O1a	O1a	O1a	O1a	O1a	O1a	O1a
O-M101	26	VII	1U	32	Eu16	H9	H	O1a	O1a1	O1a1a	O1a1a	O1a1	O1a1	O1a1a	O1a1a	O1a1a	O1a1a	O1a1a
O-M50	26	VII	1U	32	Eu16	H10	H	O1b	O1a2	O1a2	O1a2	O1a2	O1a2	O1a2	O1a2	O1a2	O1a2	O1a2
O-P31	26	VII	1U	33	Eu16	H5	I	O2*	O2	O2	O2	O2	O2	O2	O2	O2	O2	O2
O-M95	26	VII	1U	34	Eu16	H11	G	O2a*	O2a	O2a	O2a	O2a	O2a	O2a	O2a	O2a	O2a1	O2a1
O-M88	26	VII	1U	34	Eu16	H12	G	O2a1	O2a1	O2a1	O2a1	O2a1	O2a1	O2a1	O2a1	O2a1	O2a1a	O2a1a
O-SRY465	20	VII	1U	35	Eu16	H5	I	O2b*	O2b	O2b	O2b	O2b	O2b	O2b	O2b	O2b	O2b	O2b
O-47z	5	VII	1U	26	Eu16	H5	I	O2b1	O2b1a	O2b1	O2b1	O2b1a	O2b1a	O2b1	O2b1	O2b1	O2b1	O2b1
O-M122	26	VII	1U	29	Eu16	H6	L	O3*	O3	O3	O3	O3	O3	O3	O3	O3	O3	O3
O-M121	26	VII	1U	29	Eu16	H6	L	O3a	O3a	O3a1	O3a1	O3a1	O3a1	O3a1	O3a1	O3a1	O3a1a	O3a1a
O-M164	26	VII	1U	29	Eu16	H6	L	O3b	O3b	O3a2	O3a2	O3a2	O3a2	O3a2	O3a2	O3a2	O3a1b	O3a1b
O-M159	13	VII	1U	31	Eu16	H6	L	O3c	O3c	O3a3a	O3a3a	O3a3	O3a3	O3a3a	O3a3a	O3a3a	O3a3a	O3a3a
O-M7	26	VII	1U	29	Eu16	H7	L	O3d*	O3c	O3a3b	O3a3b	O3a4	O3a4	O3a3b	O3a3b	O3a3b	O3a2b	O3a2b
O-M113	26	VII	1U	29	Eu16	H7	L	O3d1	O3c1	O3a3b1	O3a3b1	-	O3a4a	O3a3b1	O3a3b1	O3a3b1	O3a2b1	O3a2b1
O-M134	26	VII	1U	30	Eu16	H8	L	O3e*	O3d	O3a3c	O3a3c	O3a5	O3a5	O3a3c	O3a3c	O3a3c	O3a2c1	O3a2c1
O-M117	26	VII	1U	30	Eu16	H8	L	O3e1*	O3d1	O3a3c1	O3a3c1	O3a5a	O3a5a	O3a3c1	O3a3c1	O3a3c1	O3a2c1a	O3a2c1a
O-M162	26	VII	1U	30	Eu16	H8	L	O3e1a	O3d1a	O3a3c1a	O3a3c1a	O3a5a1	O3a5a1	O3a3c1a	O3a3c1a	O3a3c1a	O3a2c1a1	O3a2c1a1

Original Research Publications

The following research teams per their publications were represented in the creation of the YCC Tree.

α Jobling and Tyler-Smith 2000 and Kaladjieva 2001
β Underhill 2000
γ Hammer 2001
δ Karafet 2001
ε Semino 2000
ζ Su 1999
η Capelli 2001

Phylogenetic Trees

This phylogenetic tree of haplogroup O subclades is based on the YCC 2008 tree (Karafet 2008) and subsequent published research.

O-M122 (M122, P198)
- O-P93 (M324, P93, P197, P198, P199, P200)
  - O-M121 (M121, P27.2)
  - O-M164 (M164)
  - O-P201 (P201/021354)
  - O-002611 (002611)
  - O-M300 (M300)
  - O-M333 (M333)

Evolutionary tree of human Y-chromosome DNA haplogroups ^{[χ 1]}^{[χ 2]}

	"Y-chromosomal Adam"
	A00	A0-T ^{[χ 3]}
	A0	A1^{[χ 4]}
	A1a	A1b
	A1b1	BT
	B	CT
	DE	CF
	D	E		C	F
	F1	F2	F3	GHIJK
	G	HIJK
	H	IJK
	IJ	K
	I	J		LT ^{[χ 5]}	K2
	L	T		NO ^{[χ 6]}	K2b ^{[χ 7]}	K2c	K2d	K2e ^{[χ 8]}
	N	O		K2b1 ^{[χ 9]}	P
	M	S ^{[χ 10]}		Q	R
Y-DNA by populations Famous Y-DNA haplotypes
↑ Van Oven M, Van Geystelen A, Kayser M, Decorte R, Larmuseau HD (2014). "Seeing the wood for the trees: a minimal reference phylogeny for the human Y chromosome". Human Mutation 35 (2): 187–91. doi:10.1002/humu.22468. PMID 24166809. ↑ International Society of Genetic Genealogy (ISOGG; 2015), Y-DNA Haplogroup Tree 2015. (Access date: 1 February 2015.) ↑ Haplogroup A0-T is also known as A0'1'2'3'4. ↑ Haplogroup A1 is also known as A1'2'3'4. ↑ Haplogroup LT (L298/P326) is also known as Haplogroup K1. ↑ Haplogroup NO (M214) is also known as Haplogroup K2a (although the present Haplogroup K2e was also previously known as "K2a"). ↑ Haplogroup K2b (M1221/P331/PF5911) is also known as Haplogroup MPS. ↑ Haplogroup K2e (K-M147) was previously known as "Haplogroup X" and "K2a" (but is a sibling subclade of the present K2a, also known as Haplogroup NO). ↑ Haplogroup K2b1 (P397/P399) is similiar to the former Haplogroup MS, but has a broader and more complex internal structure. ↑ Haplogroup S (S-M230) was previously known as Haplogroup K5.

References

Citations

1 2 3 Shi, Hong; Dong, Yong-li; Wen, Bo; Xiao, Chun-Jie; Underhill, Peter A.; Shen, Pei-dong; Chakraborty, Ranajit; Jin, Li; Su, Bing (Sep 2005). "Y-Chromosome Evidence of Southern Origin of the East Asian–Specific Haplogroup O3-M122". American Journal of Human Genetics 77 (408–419): 2005. doi:10.1086/444436. PMC 1226206. PMID 16080116.
↑ Kim, Soon-Hee; Kim, Ki-Cheol; Shin, Dong-Jik; Jin, Han-Jun; Kwak, Kyoung-Don; Han, Myun-Soo; Song, Joon-Myong; Kim, Won; Kim, Wook (2011). "High frequencies of Y-chromosome haplogroup O2b-SRY465 lineages in Korea: a genetic perspective on the peopling of Korea". Investigative Genetics 2 (1): 10–121. doi:10.1186/2041-2223-2-10. PMC 3087676. PMID 21463511.
1 2 3 Underhill, Peter A.; Shen, Peidong; Lin, Alice A.; et al. (November 2000). "Y chromosome sequence variation and the history of human populations". Nature Genetics 26: 358–61. doi:10.1038/81685. PMID 11062480.
↑ Wang, Chuan-Chao; Wang, Ling-Xiang; Shrestha, Rukesh; Zhang, Manfei; Huang, Xiu-Yuan; Hu, Kang; Jin, Li; Li, Hui (2014). "Genetic Structure of Qiangic Populations Residing in the Western Sichuan Corridor". PLOS ONE 9 (8): e103772. doi:10.1371/journal.pone.0103772.
↑ Wang; Yan, Shi; Dong, QIN; Lu, Yan; Qi; Liang, DING; Hai, WEI; Shi; Lin, LI; Ya; Jun, YANG; Jin, Li; Li, Hui (2013). "Late Neolithic expansion of ancient Chinese revealed by Y chromosome haplogroup O3a1c‐002611". Journal of Systematics and Evolution 51 (3): 280–286. doi:10.1111/j.1759-6831.2012.00244.x.

Sources

Journal articles

Black, M. L.; Dufall, K.; Wise, C.; Sullivan, S.; Bittles, A. H. (2006). "Genetic ancestries in northwest Cambodia". Annals of Human Biology 33 (5–6): 620–7. doi:10.1080/03014460600882561. PMID 17381059.
Cai, Xiaoyun; Qin, Zhendong; Wen, Bo; Xu, Shuhua; Wang, Yi; Lu, Yan; Wei, Lanhai; Wang, Chuanchao; et al. (2011). O'Rourke, Dennis, ed. "Human Migration through Bottlenecks from Southeast Asia into East Asia during Last Glacial Maximum Revealed by Y Chromosomes". PLoS ONE 6 (8): e24282. Bibcode:2011PLoSO...624282C. doi:10.1371/journal.pone.0024282. PMC 3164178. PMID 21904623.
Cordaux, R.; Weiss, G; Saha, N; Stoneking, M (2004). "The Northeast Indian Passageway: A Barrier or Corridor for Human Migrations?". Molecular Biology and Evolution 21 (8): 1525–33. doi:10.1093/molbev/msh151. PMID 15128876.
Gan, Rui-Jing; Pan, Shang-Ling; Mustavich, Laura F.; Qin, Zhen-Dong; Cai, Xiao-Yun; Qian, Ji; Liu, Cheng-Wu; Peng, Jun-Hua; et al. (2008). "Pinghua population as an exception of Han Chinese's coherent genetic structure". Journal of Human Genetics 53 (4): 303–13. doi:10.1007/s10038-008-0250-x. PMID 18270655.
Gayden, Tenzin; Cadenas, Alicia M.; Regueiro, Maria; Singh, Nanda B.; Zhivotovsky, Lev A.; Underhill, Peter A.; Cavalli-Sforza, Luigi L.; Herrera, Rene J. (2007). "The Himalayas as a Directional Barrier to Gene Flow". The American Journal of Human Genetics 80 (5): 884–94. doi:10.1086/516757. PMC 1852741. PMID 17436243.
Hammer, Michael F.; Karafet, Tatiana M.; Park, Hwayong; Omoto, Keiichi; Harihara, Shinji; Stoneking, Mark; Horai, Satoshi (2005). "Dual origins of the Japanese: Common ground for hunter-gatherer and farmer Y chromosomes". Journal of Human Genetics 51 (1): 47–58. doi:10.1007/s10038-005-0322-0. PMID 16328082.
He, Jun-Dong; Peng, Min-Sheng; Quang, Huy Ho; Dang, Khoa Pham; Trieu, An Vu; Wu, Shi-Fang; Jin, Jie-Qiong; Murphy, Robert W.; et al. (2012). Kayser, Manfred, ed. "Patrilineal Perspective on the Austronesian Diffusion in Mainland Southeast Asia". PLoS ONE 7 (5): e36437. Bibcode:2012PLoSO...736437H. doi:10.1371/journal.pone.0036437. PMC 3346718. PMID 22586471.
Hurles, M; Sykes, B; Jobling, M; Forster, P (2005). "The Dual Origin of the Malagasy in Island Southeast Asia and East Africa: Evidence from Maternal and Paternal Lineages". The American Journal of Human Genetics 76 (5): 894–901. doi:10.1086/430051. PMC 1199379. PMID 15793703.
Jin, Han-Jun; Tyler-Smith, Chris; Kim, Wook (2009). Batzer, Mark A, ed. "The Peopling of Korea Revealed by Analyses of Mitochondrial DNA and Y-Chromosomal Markers". PLoS ONE 4 (1): e4210. Bibcode:2009PLoSO...4.4210J. doi:10.1371/journal.pone.0004210. PMC 2615218. PMID 19148289.
Jing, Chen; Hui, LI; Zhen-Dong, QIN; Wen-Hong, LIU; Wei-Xiong, LIN; Rui-Xing, YIN; Li, JIN; Shang-Ling, PAN (2006). "Y-chromosome Genotyping and Genetic Structure of Zhuang Populations". Acta Genetica Sinica 33 (12): 1060–72. doi:10.1016/S0379-4172(06)60143-1. PMID 17185165.
Karafet, Tatiana; Xu, Liping; Du, Ruofu; Wang, William; Feng, Shi; Wells, R.S.; Redd, Alan J.; Zegura, Stephen L.; Hammer, Michael F. (2001). "Paternal Population History of East Asia: Sources, Patterns, and Microevolutionary Processes". The American Journal of Human Genetics 69 (3): 615–28. doi:10.1086/323299. PMC 1235490. PMID 11481588.
Karafet, Tatiana M.; Lansing, J. S.; Redd, Alan J.; Watkins, Joseph C.; Surata, S. P. K.; Arthawiguna, W. A.; Mayer, Laura; Bamshad, Michael; et al. (2005). "Balinese Y-Chromosome Perspective on the Peopling of Indonesia: Genetic Contributions from Pre-Neolithic Hunter-Gatherers, Austronesian Farmers, and Indian Traders". Human Biology 77 (1): 93–114. doi:10.1353/hub.2005.0030. PMID 16114819.
Katoh, Toru; Munkhbat, Batmunkh; Tounai, Kenichi; Mano, Shuhei; Ando, Harue; Oyungerel, Ganjuur; Chae, Gue-Tae; Han, Huun; Jia, Guan-Jun; Tokunaga, Katsushi; Munkhtuvshin, Namid; Tamiya, Gen; Inoko, Hidetoshi (2005). "Genetic features of Mongolian ethnic groups revealed by Y-chromosomal analysis". Gene 346: 63–70. doi:10.1016/j.gene.2004.10.023. PMID 15716011.
Kayser, M.; Brauer, S; Cordaux, R; Casto, A; Lao, O; Zhivotovsky, LA; Moyse-Faurie, C; Rutledge, RB; et al. (2006). "Melanesian and Asian Origins of Polynesians: MtDNA and Y Chromosome Gradients Across the Pacific". Molecular Biology and Evolution 23 (11): 2234–44. doi:10.1093/molbev/msl093. PMID 16923821.
Kharkov, V. N.; Stepanov, V. A.; Medvedeva, O. F.; Spiridonova, M. G.; Voevoda, M. I.; Tadinova, V. N.; Puzyrev, V. P. (2007). "Gene pool differences between Northern and Southern Altaians inferred from the data on Y-chromosomal haplogroups". Russian Journal of Genetics 43 (5): 551–562. doi:10.1134/S1022795407050110.
Kim, Wook; Yoo, Tag-Keun; Kim, Sung-Joo; Shin, Dong-Jik; Tyler-Smith, Chris; Jin, Han-Jun; Kwak, Kyoung-Don; Kim, Eun-Tak; Bae, Yoon-Sun (2007). Blagosklonny, Mikhail, ed. "Lack of Association between Y-Chromosomal Haplogroups and Prostate Cancer in the Korean Population". PLoS ONE 2 (1): e172. Bibcode:2007PLoSO...2..172K. doi:10.1371/journal.pone.0000172. PMC 1766463. PMID 17245448.
Kumar, Vikrant; Reddy, Arimanda NS; Babu, Jagedeesh P; Rao, Tipirisetti N; Langstieh, Banrida T; Thangaraj, Kumarasamy; Reddy, Alla G; Singh, Lalji; Reddy, Battini M (2007). "Y-chromosome evidence suggests a common paternal heritage of Austro-Asiatic populations". BMC Evolutionary Biology 7 (1): 47. doi:10.1186/1471-2148-7-47. PMC 1851701. PMID 17389048.
Li, Hui; Wen, Bo; Chen, Shu-Juo; Su, Bing; Pramoonjago, Patcharin; Liu, Yangfan; Pan, Shangling; Qin, Zhendong; Liu, Wenhong; Cheng, Xu; Yang, Ningning; Li, Xin; Tran, Dinhbinh; Lu, Daru; Hsu, Mu-Tsu; Deka, Ranjan; Marzuki, Sangkot; Tan, Chia-Chen; Jin, Li (2008). "Paternal genetic affinity between western Austronesians and Daic populations". BMC Evolutionary Biology 8 (1): 146. doi:10.1186/1471-2148-8-146. PMC 2408594. PMID 18482451.
Nonaka, I.; Minaguchi, K.; Takezaki, N. (2007). "Y-chromosomal Binary Haplogroups in the Japanese Population and their Relationship to 16 Y-STR Polymorphisms". Annals of Human Genetics 71 (4): 480–95. doi:10.1111/j.1469-1809.2006.00343.x. PMID 17274803.
Reddy, B. Mohan; Langstieh, B. T.; Kumar, Vikrant; Nagaraja, T.; Reddy, A. N. S.; Meka, Aruna; Reddy, A. G.; Thangaraj, K.; Singh, Lalji (2007). Awadalla, Philip, ed. "Austro-Asiatic Tribes of Northeast India Provide Hitherto Missing Genetic Link between South and Southeast Asia". PLoS ONE 2 (11): e1141. Bibcode:2007PLoSO...2.1141R. doi:10.1371/journal.pone.0001141. PMC 2065843. PMID 17989774.
Shi, Simona; Pala, Maria; Battaglia, Vincenza; Maranta, Ramona; Achilli, Alessandro; Modiano, Guido; Torroni, Antonio; Semino, Ornella; Santachiara-Benerecetti, Silvana A (2009). "Mitochondrial and Y-chromosome diversity of the Tharus (Nepal): A reservoir of genetic variation". BMC Evolutionary Biology 9 (1): 154. doi:10.1186/1471-2148-9-154. PMC 2720951. PMID 19573232.
Su, B.; Jin, L.; Underhill, P.; Martinson, J.; Saha, N.; McGarvey, S. T.; Shriver, M. D.; Chu, J.; et al. (2000). "Polynesian origins: Insights from the Y chromosome". Proceedings of the National Academy of Sciences 97 (15): 8225–8228. Bibcode:2000PNAS...97.8225S. doi:10.1073/pnas.97.15.8225. *H6 (=O-M122(xO-M7, O-M134)) in 18/73=24.7% *H8 (=O-M134) in 2/73=2.7% for a total of 20/73=27.4% O-M122 in a pool of seven samples from Micronesia. *13/40=32.5% O-M122(xM7,M134) in a pool of three samples from Polynesia. *9/27=33.3% H6 (=O-M122(xM7,M134)) *6/27=22.2% H8 (=O-M134) for a total of 15/27=55.6% O-M122 in "Malay" sample *2/19=10.5% H6 (=O-M122(xM7,M134)) in "Kota Kinabalu" sample.
Su, Bing; Xiao, Junhua; Underhill, Peter; Deka, Ranjan; Zhang, Weiling; Akey, Joshua; Huang, Wei; Shen, Di; et al. (1999). "Y-Chromosome Evidence for a Northward Migration of Modern Humans into Eastern Asia during the Last Ice Age". The American Journal of Human Genetics 65 (6): 1718–24. doi:10.1086/302680. PMC 1288383. PMID 10577926.
Tajima, Atsushi; Hayami, Masanori; Tokunaga, Katsushi; Juji, Takeo; Matsuo, Masafumi; Marzuki, Sangkot; Omoto, Keiichi; Horai, Satoshi (2004). "Genetic origins of the Ainu inferred from combined DNA analyses of maternal and paternal lineages". Journal of Human Genetics 49 (4): 187–93. doi:10.1007/s10038-004-0131-x. PMID 14997363.
Wang, Wei; Wise, Cheryl; Baric, Tom; Black, Michael L.; Bittles, Alan H. (August 1, 2003). "The origins and genetic structure of three co-resident Chinese Muslim populations: the Salar, Bo'an and Dongxiang". Human Genetics (Springer-Verlag) 113 (3): 244–52. doi:10.1007/s00439-003-0948-y. ISSN 0340-6717. PMID 12759817.
Wells, R. S.; Yuldasheva, N.; Ruzibakiev, R.; Underhill, P. A.; Evseeva, I.; Blue-Smith, J.; Jin, L.; Su, B.; et al. (2001). "The Eurasian Heartland: A continental perspective on Y-chromosome diversity". Proceedings of the National Academy of Sciences 98 (18): 10244–9. Bibcode:2001PNAS...9810244W. doi:10.1073/pnas.171305098. PMC 56946. PMID 11526236.
Wen, Bo; Li, Hui; Lu, Daru; Song, Xiufeng; Zhang, Feng; He, Yungang; Li, Feng; Gao, Yang; et al. (2004). "Genetic evidence supports demic diffusion of Han culture". Nature 431 (7006): 302–5. Bibcode:2004Natur.431..302W. doi:10.1038/nature02878. PMID 15372031.
Wen, Bo; Xie, Xuanhua; Gao, Song; Li, Hui; Shi, Hong; Song, Xiufeng; Qian, Tingzhi; Xiao, Chunjie; et al. (2004). "Analyses of Genetic Structure of Tibeto-Burman Populations Reveals Sex-Biased Admixture in Southern Tibeto-Burmans". The American Journal of Human Genetics 74 (5): 856–865. doi:10.1086/386292. PMC 1181980. PMID 15042512.
Wen, Bo; Hong, S; Ling, R; Huifeng, X; Kaiyuan, L; Wenyi, Z; Bing, S; Shiheng, S; et al. (2004). "The origin of Mosuo people as revealed by mtDNA and Y chromosome variation". Science China Life Sciences 47 (1): 1–10. doi:10.1360/02yc0207. PMID 15382670.
Xie, Xuan-Hua. "Genetic Structure of Tujia as Revealed by Y Chromosomes".
Xue, Y.; Zerjal, T; Bao, W; Zhu, S; Shu, Q; Xu, J; Du, R; Fu, S; et al. (2005). "Male Demography in East Asia: A North-South Contrast in Human Population Expansion Times". Genetics 172 (4): 2431–9. doi:10.1534/genetics.105.054270. PMC 1456369. PMID 16489223.
Yang, Zhili; Dong, Yongli; Gao, Lu; Cheng, Baowen; Yang, Jie; Zeng, Weimin; Lu, Jing; Su, Yanhua; Xiao, Chunjie (2005). "The distribution of Y chromosome haplogroups in the nationalities from Yunnan Province of China". Annals of Human Biology 32 (1): 80–7. doi:10.1080/03014460400027557. PMID 15788357.
Zhou, Ruixia; Yang, Daqun; Zhang, Hua; Yu, Weiping; An, Lizhe; Wang, Xilong; Li, Hong; Xu, Jiujin; Xie, Xiaodong (2008). "Origin and evolution of two Yugur sub-clans in Northwest China: A case study in paternal genetic landscape". Annals of Human Biology 35 (2): 198–211. doi:10.1080/03014460801922927. PMID 18428013.

Websites

Genographic Project, R. Spencer; Wells. "The Genographic Project - Atlas of the Human Journey".
Krahn; FTDNA (2003). "Genomic Research Center Draft Tree (AKA Y-TRee)".

External links

Spread of Haplogroup O-M122, from The Genographic Project, National Geographic
China DNA interest group at Facebook
China DNA Project Website at Family Tree DNA

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