Haplogroup O-M176
Haplogroup O-M176 (aka O-SRY465) or O1b2 is a human Y-chromosome DNA haplogroup. It is best known for its part in the settlement of Korea and Japan. It is a descendant of Haplogroup O-P31, and it has been estimated to share a most recent common ancestor with its nearest outgroup, Haplogroup O-K18, approximately 28,300 [95% CI 26,100 <-> 30,500] years before present,[3] approximately 29,100 years before present,[2] or approximately 31,108 (95% CI 22,844 <-> 34,893) years before present.[1]
Haplogroup O-M176
![]() O1b2-M176 | |
---|---|
Possible time of origin | 31,108 (95% CI 22,844 <-> 34,893) years ago[1] 29,100 years ago[2] 28,300 [95% CI 26,100 <-> 30,500] years ago[3] |
Coalescence age | 25,800 [95% CI 23,400 <-> 28,400] years[3] 25,660 years[2] |
Possible place of origin | Manchuria or a nearby part of northern East Asia[4][5] |
Ancestor | O-P31 |
Defining mutations | M176/SRY465, P49, 022454 |
Highest frequencies | Japanese, Koreans, Ryukyuans, Manchus
|
Distribution
Haplogroup O-M176 is found mainly in the northernmost parts of East Asia, from the Uriankhai and Zakhchin peoples of western Mongolia (Katoh et al. 2005) to the Japanese of Japan, though it also has been detected sporadically in the Buryats (Jin et al. 2003). It's been detected with moderate frequencies in Udegeys (Jin, Kim & Kim 2010) of southern Siberia, rarely among populations of Southeast Asia including Indonesia (Hammer et al. 2006 and Jin et al. 2003), the Philippines (Jin et al. 2003), Thailand (Jin et al. 2003), and Vietnam (Hammer et al. 2006 and Jin et al. 2003), and Micronesians (Hammer et al. 2006). This haplogroup is found with its highest frequency and diversity values among modern populations of Japan and Korea and is rare in most populations in China. Among Han Chinese, it has been detected in some samples of Han Chinese from Beijing (1/51, Jin et al. 2003 and Kim et al. 2011),[4] Xi'an (1/34, Kim et al. 2011),[4] one Han Chinese in Henan,[15] Han Chinese in Taiwan (2/352 = 0.57%, including one of 34 Hakka people and one of 258 miscellaneous Han volunteers),[16] Han Chinese from East China sampled from the infertility clinic at the Affiliated Hospitals of Nanjing Medical University at Jiangsu (6/1147 = 0.52%, Lu et al. 2009), Wuhan (1/160),[17] and South China outside of Jiangsu, Anhui, Zhejiang, and Shanghai (1/65).[18] Among ethnic minorities in China, haplogroup O-M176 has been detected with high frequency in samples of Koreans in China (Xue et al. 2006 and Katoh et al. 2005) and with much lower frequency among Manchus[19] (Xue et al. 2006, Katoh et al. 2005, and Karafet et al. 2001), Hezhe people,[10] Daurs,[10] Evenks,[9] Sibes (Xue et al. 2006), Kham Tibetans,[20] and Hui.[21] In a study of various populations of Hunan, O1b2-M176 was found in 0.55% (5/903) of all samples; specifically, this haplogroup was observed in 3.0% (1/33) of a sample of Iu Mien from Hunan, 1.9% (2/103) of a sample of Gàn Chinese from Hunan, 1.4% (1/71) of a sample of Kam from Hunan, and 1.1% (1/95) of a sample of Xong Miao from Hunan.[22] In a study published in July 2020, Y-DNA belonging to haplogroup O1b2-M176 was observed in 1.31% (4/305) of a sample of Han Chinese from Zibo, Shandong and in 1.06% (6/565) of a sample of Han Chinese from Zhaotong, Yunnan.[23]
Mitsuru Sakitani suggests that haplogroup O1b2, which is common in today Koreans, Japanese and Manchu, are one of the carriers of Liao civilization or Yangtze civilization. As the Liao civilization and the Yangtze civilization declined several tribes crossed westward and northerly, to the Korean Peninsula and the Japanese archipelago. However, Mitsuru Sakitani said that Currently, very little o1b2 are detected in the Yangtze River region, there are many problems in the theory that originate from the Yangtze River area.[24][25][26] Another study calls the haplogroup O1b1 as the major Austroasiatic paternal lineage and the haplogroup O1b2 (of Koreans and Japanese) as the "para-Austroasiatic" paternal lineage.[27]
Paragroup O-M176*
Y-DNA that belongs to O-M176(xK10, F3356) has been found in an individual from Hiroshima,[3] an individual from Fukushima,[3] an individual from Beijing,[3] and 1% (7/706) of a sample of males collected in Seoul and Daejeon.[28]
O-M176(x47z) has been found in approximately 3.5%[29] to 9.9%[30] of Japanese males. However, most of those individuals probably belong to subclades of O-K10(x47z).
O-K10
The majority of extant members of O-M176 belong to the subclade O-K10 (aka O-F3356 aka O-F1204). O-K10 (TMRCA 7,900 [95% CI 5,624 <-> 9,449] ybp according to Karmin et al. 2022, TMRCA 7,000 [95% CI 6,100 <-> 8,000] ybp according to YFull, TMRCA 6,980 years according to 23mofang) subsumes the prolific subclades O-47z, which occurs with especially high frequency in Japan, and O-L682, which occurs with especially high frequency in Korea, in addition to the relatively rare subclades O-CTS10687, which has been found in Japan, Korea, and China, and O-K3, which has been found among Han Chinese mostly in South Central China. O-L682 and O-K3 are linked by 18 SNPs that define the O-K4 clade, and thus their members are more closely related to one another by paternal lineage than any of them is related to any member of O-47z or O-CTS10687.
O-F3356(x47z, L682) has been found in 2% (14/706) of a sample of Koreans collected in Seoul and Daejeon, South Korea.[28] However, the status of these individuals' Y-DNA in regard to K4, K3, CTS10687, and phylogenetically equivalent SNPs has not been published.
O-CTS10687 has been found in 1.8% (1/56) of the JPT sample of Japanese from Tokyo, Japan.(Poznik et al. 2016)[3]
O-47z
Haplogroup O-47z
![]() O1b2a1a1-CTS713(47z) | |
---|---|
Possible time of origin | 7,870 [95% CI 5,720–12,630] years ago (Hammer et al. 2006) 7,100 [95% CI 6,100 <-> 8,300] ybp[3] |
Possible place of origin | Japanese Archipelago (Hammer et al. 2006) or Korean Peninsula (Jin et al. 2003) |
Ancestor | O-M176 |
Defining mutations | 47z |
Highest frequencies | Japanese, Ryukyuans, Koreans, Manchus
|
O-47z or O-CTS11986 is a subclade of O-K10. It is found with high frequency among the Japanese and Ryukyuan populations of Japan, and with lower frequency among Koreans.
Haplogroup O-47z has been detected in approximately 24% of males who speak a Japonic language, while it has not been found at all among Ainu males whose Y-DNA has been tested in two genetic studies (Tajima et al. 2004, n=16; Hammer et al. 2006, n=4). Based on the STR haplotype diversity within Haplogroup O-47z, it has been estimated in a study published in 2006 that this haplogroup has expanded from a single founder who has lived approximately 3,810 (95% CI 1,640 <–> 7,960) years before present in a model according to which continuous, pure exponential population growth is assumed.[9] In a paper published in 2016, the time to most recent common ancestor of a set of fifteen members of the O-47z clade, all from the JPT (Japanese in Tokyo, Japan) sample of the 1000 Genomes Project, was estimated to be 4,500 years using a relatively slow mutation rate (μ = 0.76 x 10−9 per bp per year as according to Qiaomei Fu et al. 2014) or 3,900 years using a relatively fast mutation rate (μ = 0.888 x 10−9 per bp per year as according to A. Helgason et al. 2015).[29] Haplogroup O-47z also has been found among samples of modern Koreans, though with low frequency in comparison to both the frequency of O-47z in samples of Japanese and the frequency of O-M176(x47z) in samples of Koreans.[4]
O-K4
O-K4 is a subclade of O-K10. It includes at least two subclades, O-L682 and O-K3, which have been estimated to share a most recent common ancestor approximately 6,000 (95% CI 4,900 <-> 7,100) years before present,[3] 6,010 years before present,[2] or 6,327 (95% CI 4,575 <-> 7,762) years before present.[1]
O-K3
Haplogroup O-F940 | |
---|---|
Possible time of origin | 6,010 ybp[2] |
Coalescence age | 2,650 years[2] |
Ancestor | O-F2868 |
Defining mutations | CTS12145, F1912, F2206, F2703, F940, K3 |
Highest frequencies | Han Chinese (Hunan 0.79%, Guangxi, Chongqing, Hubei 0.25%, Jiangxi, Sichuan 0.17%, etc.[2]) |
The O-K3 (or O-F940) lineage is a subclade of O-K4 that has been observed in three individuals from Hunan,[3] one individual from Jiangxi,[3] one individual from Shaanxi,[3] and one individual from Henan.[15] The TMRCA of the three individuals from Hunan plus the singletons from Jiangxi and Shaanxi has been estimated to be 1,250 (95% CI 750 <-> 1,950) ybp.[3]
The aforementioned individuals (except the one from Henan, whose status is unknown) are all known to share the MF61543 and CTS2403 SNPs (among others) besides the F940 and K3 SNPs. According to 23mofang, O-MF61543 is found especially in Hunan and with lower frequency in surrounding parts of south-central China and has an estimated TMRCA of 1,580 years. Other branches of O-F940 are extremely rare and have been found sporadically in individuals from various locations across northern China, with one individual from as far south as Xuzhou in the east and another from as far south as Zigong in the west.[2]
O-L682
Haplogroup O-L682
![]() O1b2a1a2a-L682 | |
---|---|
Possible time of origin | 6,327 [95% CI 4,575 <-> 7,762] ybp[1] |
Possible place of origin | Korean Peninsula or Manchuria |
Ancestor | O-M176, O-F3356 |
Defining mutations | L682 |
Highest frequencies | Koreans, Hezhen, Udege, Japanese, Ryukyuans, Manchus
|
The O-L682 subclade of O-K4 is believed to be related to Native Korean population. One study has found O-L682 Y-DNA in 19% (134/706) of Koreans sampled in Seoul and Daejeon.[28] O-L682 also has been found in Japanese in Tokyo, Okayama, Kōchi, and the US, Chinese in Liaoning and Shanxi, Shandong, and Beijing,[3] and Nanai people in China. Its descendants appear to have begun rapidly increasing in number at approximately the same time as those of its distant cousin O-47z, perhaps 4,000 years ago.[3]
- O1b2a3-CTS10687
- O1b2 - R220
- O1b2 - R144
- O1b2a-CTS3505
Phylogenetics
Phylogenetic history
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.
Phylogenetic trees
This phylogenetic tree of haplogroup O subclades is based on the YCC 2008 tree (Karafet et al. 2008) and subsequent published research.
- O1b2 (IMS-JST022454, L272.2, M176/Page63/SRY465, M302, P49, F1942/Page92)
- O1b2a (F1942/Page92)
- O1b2a1 (CTS9259)
- O1b2a1a (F3356)
- O1b2a1a1 (47z, CTS713, CTS11986)
- O1b2a1a2 (F2868, F3110, K4)
- O1b2a1a2a (L682)
- O1b2a1a2b (F940, F1912, F3390)
- O1b2a1a3 (CTS10687, F1813, F1800)
- O1b2a1b (CTS562)
- O1b2a1a (F3356)
- O1b2a2 (Page90)
- O1b2a1 (CTS9259)
- O1b2a (F1942/Page92)
Table of frequencies of O-M176
See also
Genetics
Y-DNA O subclades
Y-DNA backbone tree
References
Footnotes
- 256/800=32.0% O-M176 in a pool of all Japanese samples of (Xue et al. 2006), (Katoh et al. 2005), (Jin, Kim & Kim 2010), (Nonaka, Minaguchi & Takezaki 2007), (Poznik et al. 2016), and all non-Ainu and non-Okinawan Japanese samples of (Hammer et al. 2006).
- 202/677=29.8% O-M176 in a pool of all ethnic South Korean samples of (Hammer et al. 2006), (Xue et al. 2006), (Katoh et al. 2005), (Kim et al. 2007), and (Park 2013)
- 30/132=22.7% O-M176 in a pool of all Okinawan data from (Hammer et al. 2006) and (Nonaka, Minaguchi & Takezaki 2007)
- 30/123=24.3% O-M176 in a pool of all ethnic North Korea samples of (Jeong 2018)
- 150/628=23.9% O-47z in a pool of all non-Ainu and non-Okinawan Japanese samples of (Jin et al. 2003), (Hammer et al. 2006), (Xue et al. 2006), and (Nonaka, Minaguchi & Takezaki 2007)
- 22/132=16.7% O-47z in a pool of all Okinawan samples of (Hammer et al. 2006) and (Nonaka, Minaguchi & Takezaki 2007)
- 41/519=7.9% O-47z in a pool of all ethnic Korean samples of (Jin et al. 2003), (Hammer et al. 2006), (Xue et al. 2006), and (Kim et al. 2007)
- 9/135=6.7% O-47z in a pool of all "Manchu" or "Manchurian" samples of (Hammer et al. 2006), (Xue et al. 2006), and (Jin, Kim & Kim 2010)
- 41/519=7.9% O-L682 in a pool of all ethnic Korean samples of (Yoo 2014), (Katoh et al. 2005), and (Kim et al. 2011)
- 22/132=16.7% O-47z in a pool of all Okinawan samples of (Hammer et al. 2006) and (Nonaka, Minaguchi & Takezaki 2007)
- 150/628=23.9% O-47z in a pool of all non-Ainu and non-Okinawan Japanese samples of (Jin et al. 2003), (Hammer et al. 2006), (Xue et al. 2006), and (Nonaka, Minaguchi & Takezaki 2007)
- 9/135=6.7% O-47z in a pool of all "Manchu" or "Manchurian" samples of (Hammer et al. 2006), (Xue et al. 2006), and (Jin, Kim & Kim 2010)
Citations
- Monika Karmin, Rodrigo Flores, Lauri Saag, Georgi Hudjashov, Nicolas Brucato, Chelzie Crenna-Darusallam, Maximilian Larena, Phillip L Endicott, Mattias Jakobsson, J Stephen Lansing, Herawati Sudoyo, Matthew Leavesley, Mait Metspalu, François-Xavier Ricaut, and Murray P Cox, "Episodes of Diversification and Isolation in Island Southeast Asian and Near Oceanian Male Lineages," Molecular Biology and Evolution, Volume 39, Issue 3, March 2022, https://doi.org/10.1093/molbev/msac045
- Phylogenetic tree of haplogroup O-M268 at 23mofang
- YFull Haplogroup YTree v5.04 at 16 May 2017
- Kim et al. 2011.
- Balaresque P, Poulet N, Cussat-Blanc S, Gerard P, Quintana-Murci L, Heyer E, Jobling MA (October 2015). "Y-chromosome descent clusters and male differential reproductive success: young lineage expansions dominate Asian pastoral nomadic populations". European Journal of Human Genetics. 23 (10): 1413–1422. doi:10.1038/ejhg.2014.285. PMC 4430317. PMID 25585703.
- Katoh et al. 2005.
- "Kyeongsang Haplogroup (Korean DNA) : 네이버 블로그".
- Karafet et al. 2001.
- Hammer et al. 2006.
- Xue et al. 2006.
- Zhang X, He G, Li W, Wang Y, Li X, Chen Y, et al. (30 September 2021). "Genomic Insight Into the Population Admixture History of Tungusic-Speaking Manchu People in Northeast China". Frontiers in Genetics. 12: 754492. doi:10.3389/fgene.2021.754492. PMC 8515022. PMID 34659368.
- Bogunov et al. 2015.
- Jin, Kim & Kim 2010.
- Kharkov VN (2012). Структура и филогеография генофонда коренного населения Сибири по маркерам Y-хромосомы [The structure and phylogeography of the gene pool of the indigenous population of Siberia by Y-chromosome markers] (PDF) (Thesis) (in Russian).
- 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.
- Trejaut et al. 2014.
- Huang DX, Yang QE, Yin H, Zhai XD, Yang RZ (July 2006). "[Genetic polymorphism of 23 Y chromosome biallelic markers in Wuhan Han population]" [Genetic polymorphism of 23 Y chromosome biallelic markers in Wuhan Han population]. Yi Chuan = Hereditas (in Chinese). 28 (7): 791–798. PMID 16825164.
- Yan S, Wang CC, Li H, Li SL, Jin L (September 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.
- 新日本人の起源 神話からDNA科学へ、崎谷満 (著)
- Wang CC, Wang LX, Shrestha R, Zhang M, Huang XY, Hu K, et al. (4 August 2014). "Genetic structure of Qiangic populations residing in the western Sichuan corridor". PLOS ONE. 9 (8): e103772. Bibcode:2014PLoSO...9j3772W. doi:10.1371/journal.pone.0103772. PMC 4121179. PMID 25090432.
- 陆艳 (2011). 中国西部人群的遗传混合 [Genetic Mixture of People in Western China] (Thesis) (in Chinese).
- Xia ZY, Yan S, Wang CC, Zheng HX, Zhang F, Liu YC, et al. (9 August 2019). "Inland-coastal bifurcation of southern East Asians revealed by Hmong-Mien genomic history" (PDF). doi:10.1101/730903. S2CID 202028061.
{{cite journal}}
: Cite journal requires|journal=
(help) - Yin C, Su K, He Z, Zhai D, Guo K, Chen X, et al. (July 2020). "Genetic Reconstruction and Forensic Analysis of Chinese Shandong and Yunnan Han Populations by Co-Analyzing Y Chromosomal STRs and SNPs". Genes. 11 (7): 743. doi:10.3390/genes11070743. PMC 7397191. PMID 32635262.
- 新日本人の起源 神話からDNA科学へ、崎谷満
- 崎谷 満 (2009). DNA・考古・言語の学際研究が示す新・日本列島史 日本人集団・日本語の成立史 [New Japanese archipelago history shown by interdisciplinary research on DNA, archeology, and language Japanese group, history of establishment of Japanese] (in Japanese). 勉誠出版. ISBN 978-4-585-05394-1. OCLC 429025925.
- "遼河周辺から満洲あたりから見られる日本人の起源" [The origin of the Japanese seen from around Manchuria from around Ryokawa]. HLA haplotypes and Japanese migration (in Japanese). Archived from the original on 2016-08-26.
- Robbeets M, Savelyev A (2017). Language Dispersal Beyond Farming. John Benjamins Publishing Company. ISBN 978-90-272-6464-0.
- Kwon SY, Lee HY, Lee EY, Yang WI, Shin KJ (November 2015). "Confirmation of Y haplogroup tree topologies with newly suggested Y-SNPs for the C2, O2b and O3a subhaplogroups". Forensic Science International. Genetics. 19: 42–46. doi:10.1016/j.fsigen.2015.06.003. PMID 26103100.
- Poznik et al. 2016.
- Sato Y, Shinka T, Ewis AA, Yamauchi A, Iwamoto T, Nakahori Y (2014). "Overview of genetic variation in the Y chromosome of modern Japanese males". Anthropological Science. 122 (3): 131–136. doi:10.1537/ase.140709.
- "Kyeongsang Haplogroup (Korean DNA) : 네이버 블로그".
Sources
- Bogunov YV, Maltseva OV, Bogunova AA, Balanovskaya EV (June 2015). "The Nanai Clan Samar: The structure of gene pool based on Y-chromosome markers". Archaeology, Ethnology and Anthropology of Eurasia. 43 (2): 146–152. doi:10.1016/j.aeae.2015.09.015.
- Capelli C, Wilson JF, Richards M, Stumpf MP, Gratrix F, Oppenheimer S, et al. (February 2001). "A predominantly indigenous paternal heritage for the Austronesian-speaking peoples of insular Southeast Asia and Oceania". American Journal of Human Genetics. 68 (2): 432–443. doi:10.1086/318205. PMC 1235276. PMID 11170891.
- Di Cristofaro J, Pennarun E, Mazières S, Myres NM, Lin AA, Temori SA, 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.
- Guo; et al. (2015).
{{cite journal}}
: Cite journal requires|journal=
(help); Missing or empty|title=
(help) - Hammer MF, Karafet TM, Redd AJ, Jarjanazi H, Santachiara-Benerecetti S, Soodyall H, Zegura SL (July 2001). "Hierarchical patterns of global human Y-chromosome diversity". Molecular Biology and Evolution. 18 (7): 1189–1203. doi:10.1093/oxfordjournals.molbev.a003906. PMID 11420360.
- Hammer MF, Karafet TM, Park H, Omoto K, Harihara S, Stoneking M, Horai S (January 2006). "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.
- Hashiyada M, Umetsu K, Yuasa I, Tamura A, Matsusue A, Suzuki K, et al. (September 2008). "Population genetics of 17 Y-chromosomal STR loci in Japanese". Forensic Science International. Genetics. 2 (4): e69–e70. doi:10.1016/j.fsigen.2008.01.001. PMID 19083832.
- HGDP (2009).
{{cite journal}}
: Cite journal requires|journal=
(help); Missing or empty|title=
(help) - Jeong KS, Shin H, Lee SJ, Kim HS, Kim JY, Han MS, et al. (August 2018). "Genetic characteristics of Y-chromosome short tandem repeat haplotypes from cigarette butt samples presumed to be smoked by North Korean men". Genes & Genomics. 40 (8): 819–824. doi:10.1007/s13258-018-0701-5. PMID 30047114. S2CID 13838807.
- Jin HJ, Kwak KD, Hammer MF, Nakahori Y, Shinka T, Lee JW, et al. (December 2003). "Y-chromosomal DNA haplogroups and their implications for the dual origins of the Koreans". Human Genetics. 114 (1): 27–35. doi:10.1007/s00439-003-1019-0. PMID 14505036. S2CID 1396796.
- Jin HJ, Kim KC, Kim W (June 2010). "Genetic diversity of two haploid markers in the Udegey population from southeastern Siberia". American Journal of Physical Anthropology. 142 (2): 303–313. doi:10.1002/ajpa.21232. PMID 19953529.
- Jobling MA, Tyler-Smith C (August 2000). "New uses for new haplotypes the human Y chromosome, disease and selection". Trends in Genetics. 16 (8): 356–362. doi:10.1016/S0168-9525(00)02057-6. PMID 10904265.
- Kalaydjieva L, Calafell F, Jobling MA, Angelicheva D, de Knijff P, Rosser ZH, et al. (February 2001). "Patterns of inter- and intra-group genetic diversity in the Vlax Roma as revealed by Y chromosome and mitochondrial DNA lineages". European Journal of Human Genetics. 9 (2): 97–104. doi:10.1038/sj.ejhg.5200597. PMID 11313742. S2CID 21432405.
- Karafet T, Xu L, Du R, Wang W, Feng S, Wells RS, et al. (September 2001). "Paternal population history of East Asia: sources, patterns, and microevolutionary processes". American Journal of Human Genetics. 69 (3): 615–628. doi:10.1086/323299. PMC 1235490. PMID 11481588.
- Karafet TM, Mendez FL, Meilerman MB, Underhill PA, Zegura SL, Hammer MF (May 2008). "New binary polymorphisms reshape and increase resolution of the human Y chromosomal haplogroup tree". Genome Research. 18 (5): 830–838. doi:10.1101/gr.7172008. PMC 2336805. PMID 18385274.
- Karafet TM, Hallmark B, Cox MP, Sudoyo H, Downey S, Lansing JS, Hammer MF (August 2010). "Major east-west division underlies Y chromosome stratification across Indonesia". Molecular Biology and Evolution. 27 (8): 1833–1844. doi:10.1093/molbev/msq063. PMID 20207712.
- Katoh T, Munkhbat B, Tounai K, Mano S, Ando H, Oyungerel G, et al. (February 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.
- Kim SH, Kim KC, Shin DJ, Jin HJ, Kwak KD, Han MS, et al. (April 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. doi:10.1186/2041-2223-2-10. PMC 3087676. PMID 21463511.
- Kim W, Yoo TK, Kim SJ, Shin DJ, Tyler-Smith C, Jin HJ, et al. (January 2007). "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.
- Liu J, Guo L, Qi R, Li SY, Yin JY, Zhang W, et al. (October 2013). "Allele frequencies of 19 autosomal STR loci in Manchu population of China with phylogenetic structure among worldwide populations". Gene. 529 (2): 282–287. doi:10.1016/j.gene.2013.07.033. PMID 23928110.
- Lu C, Zhang J, Li Y, Xia Y, Zhang F, Wu B, et al. (March 2009). "The b2/b3 subdeletion shows higher risk of spermatogenic failure and higher frequency of complete AZFc deletion than the gr/gr subdeletion in a Chinese population". Human Molecular Genetics. 18 (6): 1122–1130. doi:10.1093/hmg/ddn427. PMID 19088127.
- Mizuno (2008).
{{cite journal}}
: Cite journal requires|journal=
(help); Missing or empty|title=
(help) - Nonaka I, Minaguchi K, Takezaki N (July 2007). "Y-chromosomal binary haplogroups in the Japanese population and their relationship to 16 Y-STR polymorphisms". Annals of Human Genetics. 71 (Pt 4): 480–495. doi:10.1111/j.1469-1809.2006.00343.x. hdl:10130/491. PMID 17274803. S2CID 1041367.
- Park (2012).
{{cite journal}}
: Cite journal requires|journal=
(help); Missing or empty|title=
(help) - Park (2013).
{{cite journal}}
: Cite journal requires|journal=
(help); Missing or empty|title=
(help) - Poznik GD, Xue Y, Mendez FL, Willems TF, Massaia A, Wilson Sayres MA, 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.
- Semino O, Passarino G, Oefner PJ, Lin AA, Arbuzova S, Beckman LE, et al. (November 2000). "The genetic legacy of Paleolithic Homo sapiens sapiens in extant Europeans: a Y chromosome perspective". Science. 290 (5494): 1155–1159. Bibcode:2000Sci...290.1155S. doi:10.1126/science.290.5494.1155. PMID 11073453.
- Su B, Xiao J, Underhill P, Deka R, Zhang W, Akey J, et al. (December 1999). "Y-Chromosome evidence for a northward migration of modern humans into Eastern Asia during the last Ice Age". American Journal of Human Genetics. 65 (6): 1718–1724. doi:10.1086/302680. PMC 1288383. PMID 10577926.
- Tajima A, Hayami M, Tokunaga K, Juji T, Matsuo M, Marzuki S, et al. (2004). "Genetic origins of the Ainu inferred from combined DNA analyses of maternal and paternal lineages". Journal of Human Genetics. 49 (4): 187–193. doi:10.1007/s10038-004-0131-x. PMID 14997363.
- Trejaut JA, Poloni ES, Yen JC, Lai YH, Loo JH, Lee CL, et al. (June 2014). "Taiwan Y-chromosomal DNA variation and its relationship with Island Southeast Asia". BMC Genetics. 15 (1): 77. doi:10.1186/1471-2156-15-77. PMC 4083334. PMID 24965575.
- Underhill PA, Shen P, Lin AA, Jin L, Passarino G, Yang WH, et al. (November 2000). "Y chromosome sequence variation and the history of human populations". Nature Genetics. 26 (3): 358–361. doi:10.1038/81685. PMID 11062480. S2CID 12893406.
- Xue Y, Zerjal T, Bao W, Zhu S, Shu Q, Xu J, et al. (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.
- Yoo (2014).
{{cite journal}}
: Cite journal requires|journal=
(help); Missing or empty|title=
(help)
Further reading
- Jin HJ, Tyler-Smith C, Kim W (2009). Batzer MA (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.
- Li H, Huang Y, Mustavich LF, Zhang F, Tan JZ, Wang LE, et al. (November 2007). "Y chromosomes of prehistoric people along the Yangtze River". Human Genetics. 122 (3–4): 383–388. doi:10.1007/s00439-007-0407-2. PMID 17657509. S2CID 2533393.