Draft:Haplogroup O-M176: Difference between revisions
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===Works Cited=== |
===Works Cited=== |
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{{reflist|refs= |
{{reflist|refs= |
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<ref name="Jin2003">{{cite journal|doi=10.1007/s00439-003-1019-0}}</ref> |
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<ref name="Jin2003">[http://www.springerlink.com/content/b7c224nfknj90ncy/fulltext.html Han-Jun Jin, Kyoung-Don Kwak, Michael F. Hammer, Yutaka Nakahori, Toshikatsu Shinka, Ju-Won Lee, Feng Jin, Xuming Jia, Chris Tyler-Smith and Wook Kim, "Y-chromosomal DNA haplogroups and their implications for the dual origins of the Koreans," ''Human Genetics'' (2003)]</ref> |
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<ref name="Hammer2006"> |
<ref name="Hammer2006">{{cite journal|doi=10.1007/s10038-005-0322-0|title=Dual origins of the Japanese: Common ground for hunter-gatherer and farmer Y chromosomes|year=2005|last1=Hammer|first1=Michael F.|last2=Karafet|first2=Tatiana M.|last3=Park|first3=Hwayong|last4=Omoto|first4=Keiichi|last5=Harihara|first5=Shinji|last6=Stoneking|first6=Mark|last7=Horai|first7=Satoshi|journal=Journal of Human Genetics|volume=51|pages=47–58|pmid=16328082|issue=1}}</ref> |
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<ref name="Jin2009"> |
<ref name="Jin2009">{{cite journal|doi=10.1371/journal.pone.0004210|title=The Peopling of Korea Revealed by Analyses of Mitochondrial DNA and Y-Chromosomal Markers|year=2009|editor1-last=Batzer|editor1-first=Mark A|last1=Jin|first1=Han-Jun|last2=Tyler-Smith|first2=Chris|last3=Kim|first3=Wook|journal=PLoS ONE|volume=4|pages=e4210|pmid=19148289|issue=1|pmc=2615218}}</ref> |
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<ref name="Jin2010"> |
<ref name="Jin2010">{{cite journal|doi=10.1002/ajpa.21232}}</ref> |
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<ref name="Karafet2001">{{cite journal |
<ref name="Karafet2001">{{cite journal|last1=Karafet|doi=10.1086/323299|title=Paternal Population History of East Asia: Sources, Patterns, and Microevolutionary Processes|year=2001|first1=Tatiana|last2=Xu|first2=Liping|last3=Du|first3=Ruofu|last4=Wang|first4=William|last5=Feng|first5=Shi|last6=Wells|first6=R.S.|last7=Redd|first7=Alan J.|last8=Zegura|first8=Stephen L.|last9=Hammer|first9=Michael F.|journal=The American Journal of Human Genetics|volume=69|issue=3|pages=615}}</ref> |
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<ref name="Katoh2004"> |
<ref name="Katoh2004">{{cite journal|doi=10.1016/j.gene.2004.10.023|title=Genetic features of Mongolian ethnic groups revealed by Y-chromosomal analysis|year=2005|last1=Katoh|first1=Toru|last2=Munkhbat|first2=Batmunkh|last3=Tounai|first3=Kenichi|last4=Mano|first4=Shuhei|last5=Ando|first5=Harue|last6=Oyungerel|first6=Ganjuur|last7=Chae|first7=Gue-Tae|last8=Han|first8=Huun|last9=Jia|first9=Guan-Jun|journal=Gene|volume=346|pages=63–70|pmid=15716011}}</ref> |
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<ref name="Kim2007"> |
<ref name="Kim2007">{{cite journal|doi=10.1371/journal.pone.0000172}}</ref> |
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<ref name="Lu2008">{{cite journal|doi=10.1093/hmg/ddn427}}</ref> |
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<ref name="Lu2008">Chuncheng Lu, Jie Zhang, Yingchun Li ''et al.'', "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'' Advance Access originally published online on December 16, 2008.</ref> |
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<ref name="Nonaka2007"> |
<ref name="Nonaka2007">{{cite journal|doi=10.1111/j.1469-1809.2006.00343.x|title=Y-chromosomal Binary Haplogroups in the Japanese Population and their Relationship to 16 Y-STR Polymorphisms|year=2007|last1=Nonaka|first1=I.|last2=Minaguchi|first2=K.|last3=Takezaki|first3=N.|journal=Annals of Human Genetics|volume=71|issue=4|pages=480}}</ref> |
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<ref name="Tajima2004"> |
<ref name="Tajima2004">{{cite journal|doi=10.1007/s10038-004-0131-x}}</ref> |
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<ref name="Xue2006"> |
<ref name="Xue2006">{{cite journal|doi=10.1534/genetics.105.054270}}</ref> |
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}} |
}} |
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Revision as of 00:54, 23 December 2012
Haplogroup O-M176 | |
---|---|
Possible time of origin | 6,300 [95% CI 600–37,000] years ago[1] |
Possible place of origin | Manchuria or a nearby part of northern East Asia |
Ancestor | O-P31 |
Defining mutations | M176/SRY465, P49, 022454 |
Highest frequencies | Japanese, South Koreans, Ryukyuan, and Manchu:
|
Haplogroup O-M176 (aka O-SRY465) is a human Y-chromosome DNA haplogroup. It is a descendant of Haplogroup O-P31.
Origin
This section needs expansion. You can help by adding to it. (December 2012) |
The phylogeography of Haplogroup O-M176 suggests an ancient origin in Manchuria or a nearby part of northern East Asia, followed by a long period of isolated evolution and population increase in the vicinity of the Korean Peninsula.[citation needed]
Distribution
Haplogroup O-M176 is found mainly in the northernmost parts of East Asia, from the Uriankhai and Zakhchin peoples of western Mongolia[1] to the Japanese of Japan, though it also has been detected sporadically in the Buryats[2] and Udegeys[8] of southern Siberia, very rarely among populations of Southeast Asia (including Indonesia,[5][2] the Philippines,[2] Thailand,[2] and Vietnam[5][2]), and Micronesians.[5] This haplogroup is found with its highest frequency and diversity values among modern populations of Japan and Korea and is absent from most populations in China, but it has been detected in some samples of Han Chinese from Beijing[2] and Jiangsu,[9] Daurs,[10] Hezhes,[10] Koreans in China,[10][1] Manchus,[10][1][7] and Sibes.[10]
Subclade Distribution
Paragroup O-M176*
Only branches of this haplogroup that are labeled as Haplogroup O-M176*, i.e., those that do not exhibit the 47z mutation, have been detected among the indigenous populations of Inner Mongolia and northern Manchuria, and even then they are found only at very low frequencies. However, Haplogroup O-M176* Y-chromosomes have been detected with high frequency in Korea, where they account for approximately 14%[2][3][10] to 33%[5] of the Korean male population.
O-47z
Haplogroup O-47z | |
---|---|
Possible time of origin | 7,870 [95% CI 5,720–12,630] years ago[5] |
Possible place of origin | Korean Peninsula or Japanese Archipelago[2][5] |
Ancestor | O-M176 |
Defining mutations | 47z |
Highest frequencies | Japanese 24%[Footnote 5] (19%[2]-25%[5][6]), Okinawans 17%[Footnote 6] (11%[5]-20%[6]), South Koreans 8%[Footnote 7] (4%[5][7]-12%[10]), Manchus 7%[Footnote 8] (0%[7][5][10]-19%[3]) |
A subclade of Haplogroup O-M176, Haplogroup O-47z, is found with high frequency among the Yamato people and Ryukyuan populations of Japan. Haplogroup O-47z has been detected in approximately 22% of all males who speak a Japonic language, while it has not been found at all among a total of twenty Ainu males whose Y-DNA has been sampled in two genetic studies.[5][11] Based on the STR haplotype diversity within Haplogroup O-47z, it has been estimated that this haplogroup began to experience a population expansion among the proto-Japanese of approximately 4,000 years ago, which makes it a good candidate for a marker of the intrusion of a Neolithic population of the prehistoric Korean Peninsula into the southwestern parts of the Japanese Archipelago. However, the parent haplogroup, O-M176*, is also found among Japanese, although at a relatively low frequency of approximately 4%[10] to 8%[6], and the descendant haplogroup O-47z is found only with low frequency among samples of modern Koreans, which suggests the possibility that Haplogroup O-M176* might have colonized the Japanese Archipelago much earlier, with the subgroup O-47z subsequently evolving within the proto-Japanese-Ryukyuan population of the western parts of the archipelago.
Phylogenetics
Phylogenetic History
Prior to 2002, there were in academic literature at least seven naming systems for the Y-Chromosome Phylogenetic tree. This lead 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. Latter, 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 2008) and subsequent published research.
- O-M176 (M176/SRY465, P49, 022454)
- O-47z (47z)
See also
Genetics
Y-DNA O Subclades
Y-DNA Backbone Tree
References
Footnotes
- ^ 238/744=32.0% O-M176 in a pool of all Japanese samples of Xue et al. (2006), Katoh et al. (2004), Han-Jun Jin et al. (2009), Nonaka et al. (2007), 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 Korean samples of Hammer et al. (2006), Xue et al. (2006), Katoh et al. (2004), Wook Kim et al. (2007), and Han-Jun Jin et al. (2009).
- ^ 30/132=22.7% O-M176 in a pool of all Okinawan data from Hammer et al. (2006) and Nonaka et al. (2007)
- ^ 45/232=19.4% O-M176 in a pool of all Manchu samples of Karafet et al. (2001), Han-Jun Jin et al. (2003), Katoh et al. (2004), and Xue et al. (2006)
- ^ 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 et al. (2007)
- ^ 22/132=16.7% O-47z in a pool of all Okinawan samples of Hammer et al. (2006) and Nonaka et al. (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 et al. (2009)
Works Cited
- ^ a b c d e f g Katoh, Toru; Munkhbat, Batmunkh; Tounai, Kenichi; Mano, Shuhei; Ando, Harue; Oyungerel, Ganjuur; Chae, Gue-Tae; Han, Huun; Jia, Guan-Jun (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.
- ^ a b c d e f g h i j k . doi:10.1007/s00439-003-1019-0.
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(help) - ^ a b c 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. doi:10.1371/journal.pone.0004210. PMC 2615218. PMID 19148289.
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(help)CS1 maint: unflagged free DOI (link) - ^ a b c d e f g h i j k l 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.
- ^ a b c d 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. doi:10.1111/j.1469-1809.2006.00343.x.
- ^ a b c d 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. doi:10.1086/323299.
- ^ . doi:10.1002/ajpa.21232.
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(help) - ^ . doi:10.1093/hmg/ddn427.
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(help) - ^ a b c d e f g h i . doi:10.1534/genetics.105.054270.
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(help) - ^ . doi:10.1007/s10038-004-0131-x.
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Further Reading
This section is empty. You can help by adding to it. (December 2012) |