Haplogroup R (Y-DNA): Difference between revisions
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'''Haplogroup R''', or '''R-M207''', is a [[Human Y-chromosome DNA haplogroup|Y-chromosome DNA haplogroup]]. It is both numerous and widespread amongst modern populations. |
'''Haplogroup R''', or '''R-M207''', is a [[Human Y-chromosome DNA haplogroup|Y-chromosome DNA haplogroup]]. It is both numerous and widespread amongst modern populations. |
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Some descendant [[subclade]]s have been found |
Some descendant [[subclade]]s have been found sice pre-history in [[Europe]], [[Central Asia]] and [[South Asia]]. Others have long been present, at lower levels, in parts of [[West Asia]] and [[Africa]]. Some authorities have also suggested, more controversially, that R-M207 has long been present among [[Indigenous peoples of the Americas|Native Americans]] in [[North America]] – a theory that has not yet been widely accepted. |
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Karafet et al. (2014) and other researchers state that a "rapid diversification ... of [[Haplogroup K2|K-M526]]", also known as K2, into [[Haplogroup K2a (Y-DNA)|K2a]] and [[Haplogroup K2b (Y-DNA)|K2b]] |
Karafet et al. (2014) and other researchers state that a "rapid diversification ... of [[Haplogroup K2|K-M526]]", also known as K2, into [[Haplogroup K2a (Y-DNA)|K2a]] and [[Haplogroup K2b (Y-DNA)|K2b]] |
Revision as of 06:09, 13 November 2019
Haplogroup R | |
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Possible time of origin | about 27,000 years BP[1][2] |
Possible place of origin | possibly Central Asia[3], South Asia,[4] or Siberia[5] |
Ancestor | P1 (P-M45), the only primary clade of P* (P-P295) |
Descendants | R1 (R-M173), R2 (R-M479) (R2) |
Defining mutations | M207/Page37/UTY2, CTS207/M600/PF5992, CTS2426/M661/PF6033, CTS2913/M667, CTS3229/M672/PF6036/YSC0001265, CTS3622/PF6037, CTS5815/M696, CTS6417/Y480, CTS7876/PF6052, CTS7880/M725/PF6053, CTS8311/M732, CTS9005/M741, CTS10663/M788, CTS11075/M795/P6078, CTS11647/Y369, F33/M603/PF6013, F63/M614/PF6016, F82/M620, F154/M636, F295/M685, F356/M703/PF5919, F370/M708/Y479, F459/Y482, F652/M805, F765, FGC1168, L248.3/M705.3, L747/M702/PF5918/YSC0000287, L760/M642/PF5877/YSC0000286, L1225/M789/YSC0000232, L1347/M792/PF6077/YSC0000233, M613, M628/PF5868, M651/Y296, M718, M734/PF6057/S4/YSC0000201, M760/Y506, M764/PF5953, M799, P224/PF6050, P227, P229/PF6019, P232, P280, P285, PF5938, PF6014/S9 (ISOGG 2016) |
Haplogroup R, or R-M207, is a Y-chromosome DNA haplogroup. It is both numerous and widespread amongst modern populations.
Some descendant subclades have been found sice pre-history in Europe, Central Asia and South Asia. Others have long been present, at lower levels, in parts of West Asia and Africa. Some authorities have also suggested, more controversially, that R-M207 has long been present among Native Americans in North America – a theory that has not yet been widely accepted.
Karafet et al. (2014) and other researchers state that a "rapid diversification ... of K-M526", also known as K2, into K2a and K2b , followed by K2b1 and P (also known as K2b2) "likely occurred in Southeast Asia". This was followed by the relatively rapid "westward expansion" of P1 – the immediate ancestor of both Haplogroups Q and R.[6][7]
Structure
Haplogroup R | |||||||||||||||||||||||||||||||||
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Origins
Haplogroup P1 (P-M45), the immediate ancestor of Haplogroup R, likely emerged in Southeast Asia.[6] The SNP M207, which defines Haplogroup R, is believed to have arisen during the Upper Paleolithic era, about 27,000 years ago.[2][1]
Only one confirmed example of basal R* has been found, in 24,000 year old remains, known as MA1, found at Mal'ta–Buret' culture near Lake Baikal in Siberia.[2] (While a living example of R-M207(xM17,M124) was reported in 2012, it was not tested for the SNP M478; the male concerned – among a sample of 158 ethnic Tajik males from Badakshan, Afghanistan – may therefore belong to R2.)
It is possible that neither of the primary branches of R-M207, namely R1 (R-M173) and R2 (R-M479) still exist in their basal, undivergent forms, i.e. R1* and R2*. No confirmed case, either living or dead, has been reported in scientific literature. (Although in the case of R2*, relatively little research has been completed.)
Despite the rarity of R* and R1*, the relatively rapid expansion – geographically and numerically – of subclades from R1 in particular, has often been noted: "both R1a and R1b comprise young, star-like expansions" (Karafet 2008) .
The wide geographical distribution of R1b, in particular, has also been noted. Hallast et al. (2014) mentioned that living examples found in Central Asia included:
- the "deepest subclade" of R-M269 (R1b1a1a2) – the most numerous branch of R1b in Western Europe, and;
- the rare subclade R-PH155 (R1b1b) found only in one Bhutanese individual and one Tajik.
(While Hallast et al. suggested that R-PH155 was "almost as old as the R1a/R1b split",[6] R-PH155 was later discovered to be a subclade of R-L278 (R1b1) and has been given the phylogenetic name R1b1b.)
Distribution
Y-haplogroup R-M207 is common throughout Europe, South Asia and Central Asia (Kayser 2003) . It also occurs in the Caucasus and Siberia. Some minorities in Africa also carry subclades of R-M207 at high frequencies.
While some indigenous peoples of The Americas and Australasia also feature high levels of R-M207, it is unclear whether these are deep-rooted, or an effect of European colonisation during the early modern era.
R (R-M207)
Haplogroup R* Y-DNA (xR1,R2) was found in 24,000-year-old remains from Mal'ta in Siberia near Lake Baikal.[5] In 2013, R-M207 was found in one out of 132 males from the Kyrgyz people of East Kyrgyzstan.[8]
R1 (R-M173)
R-M173, also known as R1, has been common throughout Europe and South Asia since pre-history. It has many branches (Semino 2000 and Rosser 2000 ).
It is the second most common haplogroup in Indigenous peoples of the Americas following haplogroup Q-M242, especially in the Algonquian peoples of Canada and the United States (Malhi 2008). The reasons for high levels of R-M173 among Native Americans are a matter of controversy:
- some scholars claim that this is partly or wholly the result of colonial-era immigration from Europe (see e.g. Malhi 2008), whereas;
- other authorities point to the greater similarity of many R-M173 subclades found in North America to those found in Siberia (e.g. Lell 2002 and Raghavan 2013 ), suggesting prehistoric immigration from Asia and/or Beringia.
R2 (R-M479)
Haplogroup R-M479 is defined by the presence of the marker M479. The paragroup for the R-M479 lineage is found predominantly in South Asia, although deep-rooted examples have also been found among Portuguese, Spanish, Tatar (Bashkortostan, Russia), and Ossetian (Caucasus) populations (Myres 2010) .
One rare subclade may occur only among Ashkenazi Jews, possibly as a result of a founder effect.
See also
Genetics
- Genetic history of Europe
- Genetics and archaeogenetics of South Asia
- Archaeogenetics of the Near East
- Conversion table for Y chromosome haplogroups
- Genetic genealogy
- Haplogroup
- Haplotype
- Human Y-chromosome DNA haplogroup
- Molecular phylogenetics
- Paragroup
- Subclade
- Y-chromosomal Aaron
- Y-chromosome haplogroups in populations of the world
- Y-DNA haplogroups in populations of Europe
- Y-DNA haplogroups in populations of the Near East
- Y-DNA haplogroups in populations of South Asia
- Y-DNA haplogroups in populations of North Africa
- Y-DNA haplogroups in populations of the Caucasus
- Y-DNA haplogroups by ethnic group
Y-DNA R-M207 subclades
Y-DNA backbone tree
References
- ^ a b ISOGG, Y-DNA Haplogroup R and its Subclades – 2016 (12 December 2016).
- ^ a b c Raghavan, M. et al. 2014. Upper Palaeolithic Siberian genome reveals dual ancestry of Native Americans, Nature, 505, 87–91.
- ^ karafet et al 2014.
- ^ Hallast2014.
- ^ a b Raghavan M, Skoglund P, Graf KE, Metspalu M, Albrechtsen A, Moltke I, et al. (January 2014). "Upper Palaeolithic Siberian genome reveals dual ancestry of Native Americans". Nature. 505 (7481): 87–91. Bibcode:2014Natur.505...87R. doi:10.1038/nature12736. PMC 4105016. PMID 24256729.
- ^ a b c Karafet TM, Mendez FL, Sudoyo H, Lansing JS, Hammer MF (March 2015). "Improved phylogenetic resolution and rapid diversification of Y-chromosome haplogroup K-M526 in Southeast Asia". European Journal of Human Genetics. 23 (3): 369–73. doi:10.1038/ejhg.2014.106. PMC 4326703. PMID 24896152.
- ^ See also: Tumonggor MK, Karafet TM, Downey S, Lansing JS, Norquest P, Sudoyo H, Hammer MF, Cox MP (September 2014). "Isolation, contact and social behavior shaped genetic diversity in West Timor". Journal of Human Genetics. 59 (9): 494–503. doi:10.1038/jhg.2014.62. PMC 4521296. PMID 25078354., and Heyer E, Georges M, Pachner M, Endicott P (2013). "Genetic diversity of four Filipino negrito populations from Luzon: comparison of male and female effective population sizes and differential integration of immigrants into Aeta and Agta communities". Human Biology. 85 (1–3): 189–208. doi:10.3378/027.085.0310. PMID 24297226.
- ^ Di Cristofaro J, Pennarun E, Mazières S, Myres NM, Lin AA, Temori SA, et al. (18 October 2013). "Afghan Hindu Kush: where Eurasian sub-continent gene flows converge". PLOS ONE. 8 (10): e76748. doi:10.1371/journal.pone.0076748. PMC 3799995. PMID 24204668.
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Further reading
- Myres NM, Rootsi S, Lin AA, Järve M, King RJ, Kutuev I, et al. (January 2011). "A major Y-chromosome haplogroup R1b Holocene era founder effect in Central and Western Europe". European Journal of Human Genetics. 19 (1): 95–101. doi:10.1038/ejhg.2010.146. PMC 3039512. PMID 20736979.
- Lell JT, Sukernik RI, Starikovskaya YB, Su B, Jin L, Schurr TG, Underhill PA, Wallace DC (January 2002). "The dual origin and Siberian affinities of Native American Y chromosomes". American Journal of Human Genetics. 70 (1): 192–206. doi:10.1086/338457. PMC 384887. PMID 11731934.
- Malhi (2008). "Distribution of Y Chromosomes Among Native North Americans: A Study of Athapaskan Population History" (PDF). Archived from the original (PDF) on 2010-06-17.
{{cite journal}}
: Cite journal requires|journal=
(help)CS1 maint: ref duplicates default (link) - Kivisild T, Rootsi S, Metspalu M, Mastana S, Kaldma K, Parik J, et al. (February 2003). "The genetic heritage of the earliest settlers persists both in Indian tribal and caste populations". American Journal of Human Genetics. 72 (2): 313–32. doi:10.1086/346068. PMC 379225. PMID 12536373.
- Wells RS, Yuldasheva N, Ruzibakiev R, Underhill PA, Evseeva I, Blue-Smith J, et al. (August 2001). "The Eurasian heartland: a continental perspective on Y-chromosome diversity". Proceedings of the National Academy of Sciences of the United States of America. 98 (18): 10244–9. Bibcode:2001PNAS...9810244W. doi:10.1073/pnas.171305098. PMC 56946. PMID 11526236.
- Underhill PA, Myres NM, Rootsi S, Metspalu M, Zhivotovsky LA, King RJ, et al. (April 2010). "Separating the post-Glacial coancestry of European and Asian Y chromosomes within haplogroup R1a". European Journal of Human Genetics. 18 (4): 479–84. doi:10.1038/ejhg.2009.194. PMC 2987245. PMID 19888303.
- Kivisild (2003). "The Genetic Heritage of the Earliest Settlers Persists Both in Indian Tribal and Caste Populations" (PDF).
{{cite journal}}
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(help)CS1 maint: ref duplicates default (link) - The History and Geography of Human Genes. Princeton University Press. 1994. ISBN 978-0-691-08750-4.
- 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): 830–8. doi:10.1101/gr.7172008. PMC 2336805. PMID 18385274.
- 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): 1155–9. doi:10.1126/science.290.5494.1155. PMID 11073453.
- Wells RS, Yuldasheva N, Ruzibakiev R, Underhill PA, Evseeva I, Blue-Smith J, et al. (August 2001). "The Eurasian heartland: a continental perspective on Y-chromosome diversity". Proceedings of the National Academy of Sciences of the United States of America. 98 (18): 10244–9. Bibcode:2001PNAS...9810244W. doi:10.1073/pnas.171305098. PMC 56946. PMID 11526236.
- Passarino G, Cavalleri GL, Lin AA, Cavalli-Sforza LL, Børresen-Dale AL, Underhill PA (September 2002). "Different genetic components in the Norwegian population revealed by the analysis of mtDNA and Y chromosome polymorphisms". European Journal of Human Genetics. 10 (9): 521–9. doi:10.1038/sj.ejhg.5200834. PMID 12173029.
- Behar DM, Thomas MG, Skorecki K, Hammer MF, Bulygina E, Rosengarten D, et al. (October 2003). "Multiple origins of Ashkenazi Levites: Y chromosome evidence for both Near Eastern and European ancestries". American Journal of Human Genetics. 73 (4): 768–79. doi:10.1086/378506. PMC 1180600. PMID 13680527.
- Saha A, Sharma S, Bhat A, Pandit A, Bamezai R (2005). "Genetic affinity among five different population groups in India reflecting a Y-chromosome gene flow". Journal of Human Genetics. 50 (1): 49–51. doi:10.1007/s10038-004-0219-3. PMID 15611834.
- Sengupta S, Zhivotovsky LA, King R, Mehdi SQ, Edmonds CA, Chow CE, et al. (February 2006). "Polarity and temporality of high-resolution y-chromosome distributions in India identify both indigenous and exogenous expansions and reveal minor genetic influence of Central Asian pastoralists". American Journal of Human Genetics. 78 (2): 202–21. doi:10.1086/499411. PMC 1380230. PMID 16400607.
- Cinnioglu (2004). "Excavating Y-chromosome haplotype strata in Anatolia" (PDF). Archived from the original (PDF) on 2006-06-19.
{{cite journal}}
: Cite journal requires|journal=
(help) - Underhill PA, Myres NM, Rootsi S, Metspalu M, Zhivotovsky LA, King RJ, et al. (April 2010). "Separating the post-Glacial coancestry of European and Asian Y chromosomes within haplogroup R1a". European Journal of Human Genetics. 18 (4): 479–84. doi:10.1038/ejhg.2009.194. PMC 2987245. PMID 19888303.
- Kayser M, Brauer S, Weiss G, Schiefenhövel W, Underhill P, Shen P, et al. (February 2003). "Reduced Y-chromosome, but not mitochondrial DNA, diversity in human populations from West New Guinea". American Journal of Human Genetics. 72 (2): 281–302. doi:10.1086/346065. PMC 379223. PMID 12532283.
- Firasat S, Khaliq S, Mohyuddin A, Papaioannou M, Tyler-Smith C, Underhill PA, et al. (January 2007). "Y-chromosomal evidence for a limited Greek contribution to the Pathan population of Pakistan". European Journal of Human Genetics. 15 (1): 121–6. doi:10.1038/sj.ejhg.5201726. PMC 2588664. PMID 17047675.
- Krahn, Thomas. "FTDNA Draft Y-DNA Tree (AKA YTree)". Family Tree DNA. Archived from the original on 2015-08-15.
External links
Discussion and projects