Haplogroup O-M117

Last updated
Haplogroup O-M117
Frequencies of Y-DNA haplogroup O3-M117.png
Interpolated frequency distribution [1]
Possible time of origin18,203 [95% CI 16,626 <-> 19,783] years ago (Karmin 2015 [2] )

17,430 ybp [3]

17,400 [95% CI 19,100 <-> 15,800] ybp (YFull [4] )
Coalescence age13,750 ybp [3]

12,600 [95% CI 11,300 <-> 14,000] ybp (YFull [4] )
Possible place of originprobably East Asia or Southeast Asia [ citation needed ]
Ancestor O-M134
DescendantsO-M133
Defining mutationsM117, Page23, CTS899/M1531, CTS1275/M1536, CTS3251, CTS5128/M1619, CTS6623/M1638, CTS11742/M1720, F141/M1564, F144, F235/M1587, F342/M1627, F373/M1636, F476/M1671, F579/M1692, F581, F584, F613/M1702, F649[ citation needed ]

Haplogroup O2a2b1a1-M117 or Haplogroup O2a2b1a1-M117 (also defined by the phylogenetically equivalent mutation Page23/F8/F42) is a subclade of O2a2b1-M134 (and also a subclade of haplogroup O2-M122) that occurs frequently in China and in neighboring countries like Bhutan, Nepal, and Korea, also found among Sino-Tibetan language speaking people.

Contents

O2-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% Evenki, 5/35 = 14.3% Manchu, 2/41 = 4.9% Xibe, 1/31 = 3.2% Oroqen), and Uyghurs (2/39 = 5.1% Yili, 1/31 = 3.2% Ürümqi) (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 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).

Origin

The earliest attested genealogical split within haplogroup O-M117, that between O-M133 and O-M117(xM133), is estimated to have occurred approximately 12,600 [95% CI 11,300 <-> 14,000] ybp. [4] However, members of O-M117(xM133) are quite rare among extant humans. O-M117(xM133) has been observed in 2.2% (1/46) of the CHB (Han Chinese in Beijing, China) sample of the 1000 Genomes Project. [4] In commercial testing, O-MF1380 or O-CTS4960, which belongs to O-M117(xM133), has been found in China (Beijing, Henan, Shandong, Jiangsu, Anhui, Chongqing, Guangdong), Singapore, Indonesia, Saudi Arabia, and Japan. [4] [5] O-M117(xM133) also has been found in 1.5% (2/133) of a sample collected in Daejeon, South Korea and in 1.0% (6/573) of a sample collected in Seoul, South Korea. [6] According to 23mofang, members of O-M117(xM133) comprise a subclade called O-CTS4960 (TMRCA 8,570 ybp), which is relatively concentrated in central, eastern, and northeastern areas of China and currently accounts for approximately 0.51% of the total population of males in China. [7]

The most recent common ancestor of all extant members of the O-M133 subclade, which predominates among extant members of O-M117, is estimated to have lived in a significantly less ancient era: 7,600 [95% CI 6,400 <-> 8,900] ybp according to YFull, [4] 7,455 [95% CI 6,514 <-> 8,500] years ago according to Karmin et al. 2015, [2] or 7,500 or 6,400 years ago (depending on which estimate of the mutation rate is used) according to Poznik et al. 2016. [8]

Distribution

China

Haplogroup O-M117 or O-M133 has been found often in samples of Han Chinese from various parts of China: 10/34 = 29.4% O-M133 Hakka in Taiwan, [9] 57/258 = 22.1% O-M133 miscellaneous Han volunteers in Taiwan, [9] 4/19 = 21.1% Fujian (CHS), [4] 12/60 = 20.0% O-M133 Minnan in Taiwan, [9] 29/167 = 17.4% East China, [10] 21/129 = 16.3% North China, [10] 7/46 = 15.2% Beijing (CHB), [8] 5/34 = 14.7% Chengdu, [11] 5/35 = 14.3% Harbin, [11] 9/65 = 13.8% South China, [10] 7/55 = 12.7% O-M133 Fujian, [9] 4/35 = 11.4% Meixian, [11] 75/689 = 10.9% Pudong, [12] 3/30 = 10.0% Lanzhou, [11] 50/530 = 9.4% Chongming Island, [12] 2/32 = 6.3% Yili, [11] 1/37 = 2.7% Hunan (CHS). [4]

Members of haplogroup O-M117 also have been found among various ethnic minorities in China, such as Tibetans (13/35 = 37.1%, [11] 45/156 = 28.8% [13] ), Dai (13/52 = 25.0% CDX, or Chinese Dai in Xishuangbanna), [4] She people (6/34 = 17.6% [11] ), Koreans (4/25 = 16.0% Koreans in the PRC [11] ), Hezhe (7/45 = 15.6% [11] ), Evenks (4/26 = 15.4% [11] ), Manchu (5/35 = 14.3% [11] ), Yao in Liannan, Guangdong (5/35 = 14.3% [11] ), Mongols (5/45 = 11.1% Inner Mongolian [11] ), Qiang (3/33 = 9.1% [11] ), Daurs (3/39 = 7.7% Daur [11] ), Hani (2/34 = 5.9% [11] ), Xibe (2/41 = 4.9% [11] ), Uyghurs (3/70 = 4.3% [11] ), Oroqen (1/31 = 3.2% [11] ), Buyi (1/35 = 2.9% [11] ), and Hui (1/35 = 2.9% [11] ).

Yan et al. (2014) have estimated that 16% of the present Han Chinese should be patrilineal descendants of a certain ancestor belonging to haplogroup O-M117 who has initiated a star-like population expansion dated to the Late Neolithic (5,400 [95% CI 4,100 <-> 6,700] years before present), which the authors have dubbed "Oα." [14]

According to 23mofang, haplogroup O-M117 (TMRCA 13,750 years) accounts for about 16.27% of the total male population of China, [15] with most members of O-M117 belonging to its O-F8 subclade (TMRCA 7,280 years), this latter subclade accounting for the Y-DNA of about 15.71% of all present-day Chinese males. [3] [16]

India

In a study of the DNA of Adivasi populations in the state of Meghalaya, Reddy et al. (2007) found O-M133 in 19.7% (14/71) Garo, 13.6% (6/44) Pnar, 11.1% (2/18) Nongtrai, 8.3% (5/60) Lyngngam, 6.9% (2/29) War-Khasi, 6.3% (4/64) Maram, 5.3% (1/19) War-Jaintia, 2.3% (2/87) Khynriam, and 0% (0/32) Bhoi. The Garo natively speak the Garo language, whereas all the other studied populations natively speak Khasic languages. [17]

In another study that included populations in Meghalaya, Kumar et al. (2007) found O-M133 in 9.8% (9/92) Khasi and 9.1% (3/33) Garo. [18]

A study of populations of northern West Bengal and Sikkim published in 2011 found O-M117 in 57.7% (15/26) Rabha, 47.4% (9/19) Mech, 43.1% (22/51) Rajbanshi, 41.7% (15/36) Dhimal, and 7.4% (4/54) Bengali from the northern panhandle of West Bengal and in 9.1% (1/11) of a sample of Lachungpa from Sikkim. O-M117 was not found in this study's samples of Kol (0/62), Santhal (0/51), Kharia (0/34), or Oraon (0/31) from the northern panhandle of West Bengal. [19]

Japan

A study published in the year 2000 found O-M117 in 4.3% (1/23) of a sample representing Japan. [20] 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 that should be from Kagawa Prefecture according to the geographical coordinates (134.0°E, 34.2°N) that have been provided (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). (More precisely, Nonaka et al. have found O-M117 in 1/12 = 8.3% of a sample from Shizuoka, 4/52 = 7.7% of a sample from Tokyo, 2/44 = 4.5% of a sample from Chiba, 1/2 of a sample from Gifu, 1/2 of a sample from Yamanashi, 1/3 of a sample from Hiroshima, and 1/6 of a sample from Aichi.) O-M117 has been found in 8.8% (5/57) of the JPT (Japanese in Tokyo, Japan) sample of the 1000 Genomes Project. [8] [21]

Korea

Between 11% and 15% of males in samples collected in South Korea have been found to belong to haplogroup O-M117 or O-M133 (20/133 = 15.0% Koreans in Daejeon, [6] 70/573 = 12.2% Koreans in Seoul, [6] 5/43 = 11.6% Koreans in South Korea, [11] 33/300 = 11.0% O-M133 Koreans [22] ).

Mongolia

Haplogroup O-M117 has been found in about 5% of samples of Mongols in Mongolia: 4/20 = 20.0% NE Mongolia, [23] 1/18 = 5.6% central Mongolia, [23] 3/65 = 4.6% Outer Mongolian, [11] 1/23 = 4.3% SE Mongolia, [23] 3/97 = 3.1% NW Mongolia. [23]

Nepal

Haplogroup O-M117 has been found in 84.4% (38/45) of a sample of Tamang, 33.3% of sample of Tharu of Chitwan and Morang, 21.2% (14/66) of a sample of Newar, and 16.9% (13/77) of a sample of the general population of Kathmandu. [13]

Laos

In a study published in 2011, haplogroup O-M117 has been found in 7.8% (4/51) of a sample of Hmong Daw in Laos and in 5.1% (37/728) of a set of ethnic minorities who speak various Austroasiatic languages: 32.1% (9/28) Bit, 16.2% (6/37) Kataang, 14.0% (7/50) Mal, 13.7% (7/51) Khmu, 6.9% (2/29) Xinhmul, 3.3% (1/30) Alak, 2.94% (1/34) Inh, 2.86% (1/35) Talieng, 2.0% (1/50) Laven, 2.0% (1/50) Oy, 2.0% (1/50) So, 0% (0/28) Bo, 0% (0/32) Brau, 0% (0/32) Jeh, 0% (0/35) Lamet, 0% (0/35) Ngeq, 0% (0/38) Aheu, 0% (0/39) Suy, and 0% (0/45) Katu. [24]

Kutanan et al. 2019 found O-F8/F42, which is currently considered to be phylogenetically equivalent to O-M133, in 25.0% (5/20) of a sample of Laotians from Luang Prabang and 5.0% (1/20) of a sample of Laotians from Vientiane. [25]

Thailand

In a study published in 2014, haplogroup O-M133 has been found in 13.3% (10/75) of a sample of the general population of Bangkok and in 3.7% (1/27) of a sample of Akka from Chiang Mai. [9]

Brunelli et al. (2017) have found O-M117 in 35.0% (7/20) of Shan, 22.4% (46/205) of Khon Mueang, 22.2% (4/18) of Mon, 20.0% (5/25) of Western Lawa, 17.6% (16/91) of Tai Lue, 16.7% (4/24) of Tai Khuen, 13.6% (9/66) of Tai Yuan, and 11.5% (3/26) of Tai Yong in Northern Thailand and in 31.6% (6/19) of Tai Yuan in Central Thailand. [26] However, in the same study, haplogroup O-M117 was not observed in a sample of 25 Eastern Lawa in Northern Thailand. [26]

Kutanan et al. (2019) have found O-F8/F42 (equivalent to O-M133) in 14.75% (131/888) of a pool of samples from Thailand, including 50.0% (9/18) Palaung in Northern Thailand, 38.9% (7/18) Shan in Northern Thailand, 33.3% (20/60) Khon Mueang in Northern Thailand, 31.0% (13/42) Karen in Northern Thailand, 28.6% (6/21) Nyahkur in Northeast Thailand, 23.5% (4/17) Kaleun, 17.1% (22/129) Thai (Siamese), 16.7% (5/30) Tai Lue in Northern Thailand, 16.7% (3/18) Nyaw in Northeast Thailand, 16.7% (3/18) Blang in Northern Thailand, 15.4% (4/26) Tai Yuan, 14.3% (15/105) Mon, 14.3% (5/35) Phuan, 11.8% (2/17) Soa, 11.8% (2/17) Tai Khün, 9.4% (3/32) Western Lawa, 8.3% (3/36) Black Tai, 6.5% (4/62) Lao Isan, and 5.6% (1/18) Khmu. [25]

Vietnam

Haplogroup O-M133 has been found in 4/46 = 8.7% of the KHV (Kinh in Ho Chi Minh City, Vietnam) sample of the 1000 Genomes Project. [8] [4] Haplogroup O-M133 has been found in 1/24 = 4.17% of a sample of people in Hanoi, Vietnam. [9] A study published in 2011 found haplogroup O-M117 in 1/15 = 6.67% Kinh and 1/12 = 8.33% Muong. [24]

Macholdt et al. 2020 have found O-F8, which is currently considered to be phylogenetically equivalent to O-M1706 or O-M133, in 36.4% (12/33) of a sample of Hanhi from Mường Tè District, 22.2% (8/36) of a sample of Lachi from Hoàng Su Phì District, 14.9% (7/47) of a sample of Tay, 14.3% (3/21) of a sample of Phula from Xín Mần District, 12.9% (4/31) of a sample of Lahu from Mường Tè District, 8.3% (2/24) of a sample of Thai, 4.8% (2/42) of a sample of Kinh from Hanoi, 3.7% (1/27) of a sample of Giarai, 2.8% (1/36) of a sample of Pathen, and 2.7% (1/37) of a sample of Nung from Vietnam. [27] All members of O-F8 among the Hanhi and Lahu of Mường Tè District belonged to the O-F2137 subclade. One Tay individual from Mường Khương District belonged to the O-F155 subclade and one Tay individual from Tràng Định District belonged to the O-F317 subclade. All other members of O-F8 belonged to the O-F8(xF155, F2137, F317) paragroup. Only one individual in this study (a Tay from Đức Trọng District) has been assigned to O-P164(xF8, F46, F4110) and therefore potentially might belong to O-M117(xF8/M133).

Subclades

According to the ISOGG experiental tree, the subclades of O2ab1a1-M117 are shown below (Owen Lu et al. 2016):

Related Research Articles

<span class="mw-page-title-main">Haplogroup J-M172</span> Human Y-chromosome DNA haplogroup

In human genetics, Haplogroup J-M172 or J2 is a Y-chromosome haplogroup which is a subclade (branch) of haplogroup J-M304. Haplogroup J-M172 is common in modern populations in Western Asia, Central Asia, South Asia, Southern Europe, Northwestern Iran and North Africa. It is thought that J-M172 may have originated in the Caucasus, Anatolia and/or Western Iran.

<span class="mw-page-title-main">Haplogroup A (Y-DNA)</span> Human Y-chromosome DNA haplogroup

Haplogroup A is a human Y-chromosome DNA haplogroup, which includes all living human Y chromosomes. Bearers of extant sub-clades of haplogroup A are almost exclusively found in Africa, in contrast with haplogroup BT, bearers of which participated in the Out of Africa migration of early modern humans. The known branches of haplogroup A are A00, A0, A1a, and A1b1; these branches are only very distantly related, and are not more closely related to each other than they are to haplogroup BT.

<span class="mw-page-title-main">Haplogroup B-M60</span> Human Y chromosome DNA grouping indicating common ancestry

Haplogroup B (M60) is a human Y-chromosome DNA haplogroup common to paternal lineages in Africa. It is a primary branch of the haplogroup BT.

<span class="mw-page-title-main">Haplogroup C-M130</span> Human Y chromosome DNA grouping found primarily in Asia

Haplogroup C is a major Y-chromosome haplogroup, defined by UEPs M130/RPS4Y711, P184, P255, and P260, which are all SNP mutations. It is one of two primary branches of Haplogroup CF alongside Haplogroup F. Haplogroup C is found in ancient populations on every continent except Africa and is the predominant Y-DNA haplogroup among males belonging to many peoples indigenous to East Asia, Central Asia, Siberia, North America and Australia as well as a some populations in Europe, the Levant, and later Japan.

Haplogroup D1 or D-M174 is a subclade of haplogroup D-CTS3946. This male haplogroup is found primarily in East Asia, Magar-ethnic Nepal and the Andaman Islands. It is also found regularly with lower frequency in Central Asia, Siberia and Mainland Southeast Asia, and, more rarely, in Europe and the Middle East.

<span class="mw-page-title-main">Haplogroup L-M20</span> Human Y chromosome DNA grouping common in South Asia and the Mediterranean

Haplogroup L-M20 is a human Y-DNA haplogroup, which is defined by SNPs M11, M20, M61 and M185. As a secondary descendant of haplogroup K and a primary branch of haplogroup LT, haplogroup L currently has the alternative phylogenetic name of K1a, and is a sibling of haplogroup T.

Haplogroup O-M122 is an Eastern Eurasian Y-chromosome haplogroup. The lineage ranges across Southeast Asia and East Asia, where it dominates the paternal lineages with extremely high frequencies. It is also significantly present in Central Asia, especially among the Naiman tribe of Kazakhs.

<span class="mw-page-title-main">Haplogroup Q-M242</span> Human Y chromosome DNA grouping common among Native Americans

Haplogroup Q or Q-M242 is a Y-chromosome DNA haplogroup. It has one primary subclade, Haplogroup Q1 (L232/S432), which includes numerous subclades that have been sampled and identified in males among modern populations.

<span class="mw-page-title-main">Haplogroup R1</span> Y-chromosome DNA haplogroup

Haplogroup R1, or R-M173, is a Y-chromosome DNA haplogroup. A primary subclade of Haplogroup R (R-M207), it is defined by the SNP M173. The other primary subclade of Haplogroup R is Haplogroup R2 (R-M479).

<span class="mw-page-title-main">Haplogroup R (Y-DNA)</span> Human Y-chromosome DNA haplogroup

Haplogroup R, or R-M207, is a Y-chromosome DNA haplogroup. It is both numerous and widespread among modern populations.

In human genetics, Haplogroup O-M268, also known as O1b, is a Y-chromosome DNA haplogroup. Haplogroup O-M268 is a primary subclade of haplogroup O-F265, itself a primary descendant branch of Haplogroup O-M175.

In human genetics, Haplogroup O-M119 is a Y-chromosome DNA haplogroup. Haplogroup O-M119 is a descendant branch of haplogroup O-F265 also known as O1a, one of two extant primary subclades of Haplogroup O-M175. The same clade previously has been labeled as O-MSY2.2.

<span class="mw-page-title-main">Haplogroup NO1</span> Human Y-chromosome DNA haplogroup

Haplogroup NO1, also known as NO-M214, is a human Y-chromosome DNA haplogroup. NO1 is the sole confirmed subclade of Haplogroup K- M2313, which is the sole subclade of Haplogroup K2a (K-M2308). NO is the dominant Y-DNA haplogroup in most parts of eastern and northern Eurasia, including East Asia, Siberia and northern Fennoscandia.

In human mitochondrial genetics, Haplogroup G is a human mitochondrial DNA (mtDNA) haplogroup.

<span class="mw-page-title-main">Haplogroup S-M230</span> Human Y-chromosome DNA haplogroup

Haplogroup S-M230, also known as S1a1b, is a Y-chromosome DNA haplogroup. It is by far the most numerically significant subclade of Haplogroup S1a.

<span class="mw-page-title-main">Haplogroup R1a</span> Human Y-chromosome DNA haplogroup

Haplogroup R1a, or haplogroup R-M420, is a human Y-chromosome DNA haplogroup which is distributed in a large region in Eurasia, extending from Scandinavia and Central Europe to Central Asia, southern Siberia and South Asia.

Haplogroup E-M132, formerly known as E-M33 (E1a), is a human Y-chromosome DNA haplogroup. Along with E-P177, it is one of the two main branches of the older E-P147 paternal clade. E-M132 is divided into two primary sub-branches, E-M44 and E-Z958, with many descendant subclades.

Haplogroup E-M75 is a human Y-chromosome DNA haplogroup. Along with haplogroup E-P147, it is one of the two main branches of the older haplogroup E-M96.

Haplogroup E-P2, also known as E1b1, is a human Y-chromosome DNA haplogroup. E-P2 has two basal branches, E-V38 and E-M215. E-P2 had an ancient presence in East Africa and the Levant; presently, it is primarily distributed in Africa where it may have originated, and occurs at lower frequencies in the Middle East and Europe.

<span class="mw-page-title-main">Haplogroup R-M269</span> Gene group

Haplogroup R-M269 is the sub-clade of human Y-chromosome haplogroup R1b that is defined by the SNP marker M269. According to ISOGG 2020 it is phylogenetically classified as R1b1a1b. It underwent intensive research and was previously classified as R1b1a2, R1b1c, R1b1b2 and R1b1a1a2.

References

Citations

  1. ↑ O'Rourke, Dennis; Cai, Xiaoyun; Qin, Zhendong; Wen, Bo; Xu, Shuhua; Wang, Yi; Lu, Yan; Wei, Lanhai; Wang, Chuanchao; Li, Shilin; Huang, Xingqiu; Jin, Li; Li, Hui (2011). "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 . ISSN   1932-6203. PMC   3164178 . PMID   21904623.
  2. 1 2 Karmin, Monika; Saag, Lauri; Vicente, Mário; et al. (2015). "A recent bottleneck of Y chromosome diversity coincides with a global change in culture". Genome Research. 25 (4): 459–466. doi:10.1101/gr.186684.114. PMC   4381518 . PMID   25770088.
  3. 1 2 3 Phylogenetic tree of human Y-DNA at 23mofang
  4. 1 2 3 4 5 6 7 8 9 10 YFull Haplogroup YTree v6.03.46 at 31 July 2018
  5. ↑ Phylogenetic tree of haplogroup O-M117/O-Page23 according to Family Tree DNA
  6. 1 2 3 Jin Park, Myung; Young Lee, Hwan; Ick Yang, Woo; Shin, Kyoung-Jin (2012). "Understanding the Y chromosome variation in Korea—relevance of combined haplogroup and haplotype analyses". International Journal of Legal Medicine. 126 (4): 589–599. doi:10.1007/s00414-012-0703-9. PMID   22569803. S2CID   27644576.
  7. ↑ "O-Cts4960单倍群详情".
  8. 1 2 3 4 Poznik, G. David; Xue, Yali; Mendez, Fernando L.; et al. (June 2016). "Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences". Nature Genetics. 48 (6): 593–599. doi:10.1038/ng.3559. PMC   4884158 . PMID   27111036.
  9. 1 2 3 4 5 6 Trejaut, Jean A; Poloni, Estella S; Yen, Ju-Chen; Lai, Ying-Hui; Loo, Jun-Hun; Lee, Chien-Liang; He, Chun-Lin; Lin, Marie (2014). "Taiwan Y-chromosomal DNA variation and its relationship with Island Southeast Asia". BMC Genetics. 2014 (15): 77. doi: 10.1186/1471-2156-15-77 . PMC   4083334 . PMID   24965575.
  10. 1 2 3 Yan, Shi; Wang, Chuan-Chao; Li, Hui; Li, Shi-Lin; Jin, Li (2011). "An updated tree of Y-chromosome Haplogroup O and revised phylogenetic positions of mutations P164 and PK4". European Journal of Human Genetics. 19 (9): 1013–1015. doi: 10.1038/ejhg.2011.64 . PMC   3179364 . PMID   21505448.
  11. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 Xue, Yali; Zerjal, Tatiana; Bao, Weidong; Zhu, Suling; Shu, Qunfang; Xu, Jiujin; Du, Ruofu; Fu, Songbin; Li, Pu; Hurles, Matthew E.; Yang, Huanming; Tyler-Smith, Chris (April 2006). "Male Demography in East Asia: A North–South Contrast in Human Population Expansion Times". Genetics. 172 (4): 2431–2439. doi:10.1534/genetics.105.054270. PMC   1456369 . PMID   16489223.
  12. 1 2 Zhang, X.; Tang, Z.; Wang, B.; Zhou, X.; Zhou, L.; Zhang, G.; Tian, J.; Zhao, Y.; Yao, Z.; Tian, L.; et al. "Forensic Analysis and Genetic Structure Construction of Chinese Chongming Island Han Based on Y Chromosome STRs and SNPs." Genes 2022, 13, 1363. https://doi.org/10.3390/genes13081363
  13. 1 2 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". American Journal of Human Genetics. 80 (5): 884–894. doi:10.1086/516757. PMC   1852741 . PMID   17436243.
  14. ↑ Yan S, Wang CC, Zheng HX, Wang W, Qin ZD, Wei LH, et al. (2014). "Y chromosomes of 40% Chinese descend from three Neolithic super-grandfathers". PLOS ONE. 9 (8): e105691. arXiv: 1310.3897 . Bibcode:2014PLoSO...9j5691Y. doi: 10.1371/journal.pone.0105691 . PMC   4149484 . PMID   25170956.
  15. ↑ "O-M117单倍群详情".
  16. ↑ "O-F8单倍群详情".
  17. ↑ Reddy, BM; Langstieh, BT; Kumar, V; Nagaraja, T; Reddy, ANS; et al. (2007). "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.
  18. ↑ Kumar, Vikrant; Reddy, Arimanda NS; Babu, Jagedeesh P; et al. (2007). "Y-chromosome evidence suggests a common paternal heritage of Austro-Asiatic populations". BMC Evolutionary Biology. 2007 (7): 47. Bibcode:2007BMCEE...7...47K. doi: 10.1186/1471-2148-7-47 . PMC   1851701 . PMID   17389048.
  19. ↑ Debnath, Monojit; Palanichamy, Malliya G; Mitra, Bikash; Jin, Jie-Qiong; Chaudhuri, Tapas K; Zhang, Ya-Ping (2011). "Y-chromosome haplogroup diversity in the sub-Himalayan Terai and Duars populations of East India". Journal of Human Genetics. 56 (11): 765–771. doi: 10.1038/jhg.2011.98 . PMID   21900945.
  20. ↑ Peter A. Underhill, Peidong Shen, Alice A. Lin et al., "Y chromosome sequence variation and the history of human populations," Nature Genetics • Volume 26 • November 2000
  21. ↑ YFull Haplogroup YTree v5.08 at 14 November 2017
  22. ↑ Jin Park, Myung; Young Lee, Hwan; Young Kim, Na; Young Lee, Eun; Ick Yang, Woo; Shin, Kyoung-Jin (2013). "Y-SNP miniplexes for East Asian Y-chromosomal haplogroup determination in degraded DNA". Forensic Science International: Genetics. 7 (1): 75–81. doi:10.1016/j.fsigen.2012.06.014. PMID   22818129.
  23. 1 2 3 4 Di Cristofaro, J; Pennarun, E; Mazières, S; Myres, NM; Lin, AA; et al. (2013). "Afghan Hindu Kush: Where Eurasian Sub-Continent Gene Flows Converge". PLOS ONE. 8 (10): e76748. Bibcode:2013PLoSO...876748D. doi: 10.1371/journal.pone.0076748 . PMC   3799995 . PMID   24204668.
  24. 1 2 Cai, X; Qin, Z; Wen, B; Xu, S; Wang, Y; et al. (2011). "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.
  25. 1 2 Wibhu Kutanan, Jatupol Kampuansai, Metawee Srikummool, Andrea Brunelli, Silvia Ghirotto, Leonardo Arias, Enrico Macholdt, Alexander Hübner, Roland Schröder, and Mark Stoneking (2019), "Contrasting paternal and maternal genetic histories of Thai and Lao populations."
  26. 1 2 Brunelli, A; Kampuansai, J; Seielstad, M; Lomthaisong, K; Kangwanpong, D; Ghirotto, S; et al. (2017). "Y chromosomal evidence on the origin of northern Thai people". PLOS ONE. 12 (7): e0181935. Bibcode:2017PLoSO..1281935B. doi: 10.1371/journal.pone.0181935 . PMC   5524406 . PMID   28742125.
  27. ↑ Enrico Macholdt, Leonardo Arias, Nguyen Thuy Duong, et al. (2020), "The paternal and maternal genetic history of Vietnamese populations." European Journal of Human Genetics (2020) 28:636–645. https://doi.org/10.1038/s41431-019-0557-4

Sources

Journal articles
This page is based on this Wikipedia article
Text is available under the CC BY-SA 4.0 license; additional terms may apply.
Images, videos and audio are available under their respective licenses.