词条 | Haplogroup M (mtDNA) |
释义 |
|name=M |map=Peopling of eurasia.jpg |origin-date=60,000 years before present |origin-place=South Asia[1][2][3][4][1][6]later Southeast Asia[2] [3] |ancestor=L3 |descendants=M1, M2, M3, M4'45, M5, M6, M7, M8, M9, M10'42, M12'G, M13, M14, M15, M21, M27, M28, M29'Q, M31'32, M33, M34, M35, M36, M39, M40, M41, M44, M46, M47'50, M48, M49, M51, D |mutations=263, 489, 10400, 14783, 15043[9] }} Haplogroup M is a human mitochondrial DNA (mtDNA) haplogroup. An enormous haplogroup spanning all the continents, the macro-haplogroup M, like its sibling the macro-haplogroup N, is a descendant of the haplogroup L3. All mtDNA haplogroups considered native outside of Africa are descendants of either haplogroup M or its sibling haplogroup N.[10] Haplogroup M is relatively young, having a younger most recent common ancestor date than some subclades of haplogroup N such as haplogroup R.[4] OriginsThere is a debate concerning geographical origins of Haplogroup M and its sibling haplogroup N. Both lineages are thought to have been the main surviving lineages involved in the out of Africa migration (or migrations) because all indigenous lineages found outside Africa belong to haplogroup M or haplogroup N. Yet to be conclusively determined is whether the mutations that define haplogroups M and N occurred in Africa before the exit from Africa or in Asia after the exit from Africa. Determining the origins of haplogroup M is further complicated by the fact that it is found in Africa and outside of Africa.[5] It is generally accepted that haplogroup M evolved shortly after the emergence of its parent clade haplogroup L3. Apart from haplogroup M and its sibling haplogroup N, the numerous other subclades of L3 are largely restricted to Africa, which suggests that L3 arose in Africa. Haplogroup M1Much of discussion concerning the origins of haplogroup M has been related to its subclade haplogroup M1, which is the only variant of macrohaplogroup M found in Africa.[10] Two possibilities were being considered as potential explanations for the presence of M1 in Africa:
Haplogroup M23In 2009, two independent publications reported a rare, deep-rooted subclade of haplogroup M, referred to as M23, that is present in Madagascar.[7][8] The contemporary populations of Madagascar were formed in the last 2,000 years by the admixture of Bantu and Indonesian (Austronesian) populations. M23 seems to be restricted to Madagascar, as it has not been detected anywhere else. M23 could have been brought to Madagascar from Asia where most deep rooted subclades of Haplogroup M are found. Asian origin hypothesisAccording to this theory, anatomically modern humans carrying ancestral haplogroup L3 lineages were involved in the Out of Africa migration from East Africa into Asia. Somewhere in Asia, the ancestral L3 lineages gave rise to haplogroups M and N. The ancestral L3 lineages were then lost by genetic drift as they are infrequent outside Africa. The hypothesis of Asia as the place of origin of macrohaplogroup M is supported by the following:
African origin hypothesisAccording to this theory, haplogroups M and N arose from L3 in an East African population that had been isolated from other African populations. Members of this population were involved in the out Africa migration and only carried M and N lineages. With the possible exception of haplogroup M1, all other M and N clades in Africa were lost by genetic drift.[14][6] The African origin of Haplogroup M is supported by the following arguments and evidence.
This study provides evidence that M1, or its ancestor, had an Asiatic origin. The earliest M1 expansion into Africa occurred in northwestern instead of northeastern areas; this early spread reached the Iberian Peninsula even affecting the Basques. The majority of the M1a lineages found outside and inside Africa had a more recent eastern Africa origin. Both western and eastern M1 lineages participated in the Neolithic colonization of the Sahara. The striking parallelism between subclade ages and geographic distribution of M1 and its North African U6 counterpart strongly reinforces this scenario. Finally, a relevant fraction of M1a lineages present today in the European Continent and nearby islands possibly had a Jewish instead of the commonly proposed Arab/Berber maternal ascendance.[15] DispersalA number of studies have proposed that the ancestors of modern haplogroup M dispersed from Africa through the southern route across the Horn of Africa along the coastal regions of Asia onwards to New Guinea and Australia. These studies suggested that the migrations of haplogroups M and N occurred separately with haplogroup N heading northwards from East Africa to the Levant. However, the results of numerous recent studies indicate that there was only one migration out of Africa and that haplogroups M and N were part of the same migration. This is based on the analysis of a number of relict populations along the proposed beachcombing route from Africa to Australia, all of which possessed both haplogroups N and M.[16][17] A 2008 study by Abu-Amero et al., suggests that the Arabian Peninsula may have been the main route out of Africa. However, as the region lacks of autochthonous clades of haplogroups M and N the authors suggest that the area has been a more recent receptor of human migrations than an ancient demographic expansion center along the southern coastal route as proposed under the single migration Out-of-Africa scenario of the African origin hypothesis.[18] DistributionM is the single most common mtDNA haplogroup in Asia,[19] and peaks in Japan and Tibet, where it represents on average about 70% of the maternal lineages (160/216 = 74% Tibet,[46] 205/282 = 73% Tōkai,[20] 231/326 = 71% Okinawa,[20] 148/211 = 70% Japanese,[10] 50/72 = 69% Tibet,[46] 150/217 = 69% Hokkaidō,[21] 24/35 = 69% Zhongdian Tibetan, 175/256 = 68% northern Kyūshū,[20] 38/56 = 68% Qinghai Tibetan, 16/24 = 67% Diqing Tibetan, 66/100 = 66% Miyazaki, 33/51 = 65% Ainu, 214/336 = 64% Tōhoku,[20] 75/118 = 64% Tokyo (JPT)[54]) and is ubiquitous in India[9][22][23] and South Korea,[20][24][25][61][26] where it has approximately 60% frequency. Among Chinese people both inside and outside of China, haplogroup M accounts for approximately 50% of all mtDNA on average, but the frequency varies from approximately 40% in Hans from Hunan and Fujian in southern China to approximately 60% in Shenyang, Liaoning in northeastern China.[46][20][54][25] Haplogroup M accounts for approximately 42% of all mtDNA in Filipinos, among whom it is represented mainly by M7c3c and E.[67] In Vietnam, haplogroup M has been found in 37% (52/139) to 48% (20/42) of samples of Vietnamese and in 32% (54/168) of a sample of Chams from Bình Thuận Province.[25][27] Haplogroup M accounts for 43% (92/214) of all mtDNA in a sample of Laotians, with its subclade M7 (M7b, M7c, and M7e) alone accounting for a full third of all haplogroup M, or 14.5% (31/214) of the total sample.[28] In Oceania, Haplogroup M has been found in 35% (17/48) of a sample of Papua New Guinea highlanders from the Bundi area and in 28% (9/32) of a sample of Aboriginal Australians from Kalumburu in northwestern Australia.[29] A study published in 2008 found Haplogroup M in 42% (60/144) of a pool of samples from nine language groups in the Admiralty Islands of Papua New Guinea, of which 50 belonged to typically Near Oceanian subclades (Q1, Q2) and 10 belonged to typically East or Southeast Asian subclades (M7b, M7c1c, E1b).[30] In a study published in 2015, Haplogroup M was found in 21% (18/86) of a sample of Fijians and in 0% (0/21) of a sample of Rotumans.[31] Haplogroup M is also relatively common in Northeast Africa, occurring especially among Somalis, Libyans and Oromos at frequencies over 20%.[32][33] Toward the northwest, the lineage is found at comparable frequencies among the Tuareg in Mali and Burkina Faso; particularly the M1a2 subclade (18.42%).[34] Due to its great age, haplogroup M is an mtDNA lineage which does not correspond well to present-day ethnic groups. It is found among Siberian, Native American, East Asian, Southeast Asian, Central Asian, South Asian, Melanesian, European, Northeast African, and various Middle Eastern populations at varying frequencies. Among the descendant lineages of haplogroup M are C, D, E, G, Q, and Z. Z and G are found in North Eurasian populations, C and D exists among North Eurasian and Native American populations, E is observed in Southeast Asian populations, and Q is common among Melanesian populations. The lineages M2, M3, M4, M5, M6, M18 and M25 are exclusive to South Asia, with M2 reported to be the oldest lineage on the Indian sub-continent.[9] In 2013, four ancient specimens dated to around 2,500 BC-500 AD, which were excavated from the Tell Ashara (Terqa) and Tell Masaikh (Kar-Assurnasirpal) archaeological sites in the Euphrates Valley, were found to belong to mtDNA haplotypes associated with the M4b1, M49 and/or M61 haplogroups. Since these clades are not found among the current inhabitants of the area, they are believed to have been brought at a more remote period from east of Mesopotamia; possibly by either merchants or the founders of the ancient Terqa population.[35] In 2016, three Late Pleistocene European hunter-gatherers were also found to carry M lineages. Two of the specimens were from the Goyet archaeological site in Belgium and were dated to 34,000 and 35,000 years ago, respectively. The other ancient individual hailed from the La Rochette site in France, and was dated to 28,000 years ago.[36] Ancient DNA analysis of Iberomaurusian skeletal remains at the Taforalt site in Morocco, which have been dated to between 15,100 and 13,900 ybp, observed the M1b subclade among one of the fossils (1/7; ~14%).[37] Ancient individuals belonging to the Late Iron Age settlement of Çemialo Sırtı in Batman, southeast Turkey were found to carry haplogroup M; specifically the M1a1 subclade (1/12; ~8.3%). Haplogroup M was also detected in ancient specimens from Southeast Anatolia (0.4%).[38] Additionally, M1 has been observed among ancient Egyptian mummies excavated at the Abusir el-Meleq archaeological site in Middle Egypt, which date from the Pre-Ptolemaic/late New Kingdom and Roman periods.[39] Fossils at the Early Neolithic site of Ifri n'Amr or Moussa in Morocco, which have been dated to around 5,000 BCE, have also been found to carry the M1 subclade. These ancient individuals bore an autochthonous Maghrebi genomic component that peaks among modern Berbers, indicating that they were ancestral to populations in the area.[40] The ancient Egyptian aristocrats Nakht-Ankh and Khnum-Nakht were also found to belong to the M1a1 subclade. The half-brothers lived during the 12th Dynasty, with their tomb located at the Deir Rifeh cemetery in Middle Egypt.[41] Subgroups distribution
SubcladesTreeThis phylogenetic tree of haplogroup M subclades is based on the paper by Mannis van Oven and Manfred Kayser Updated comprehensive phylogenetic tree of global human mitochondrial DNA variation[68] and subsequent published research.
See also{{Commons category|Haplogroup M (mtDNA)}}
References1. ^{{cite journal|title=Most of the extant mtDNA boundaries in South and Southwest Asia were likely shaped during the initial settlement of Eurasia by anatomically modern humans|last=Kivisild|year=2004|doi=10.1186/1471-2156-5-26|pmid=15339343|first1=M|last2=Kivisild|first2=T|last3=Metspalu|first3=E|last4=Parik|first4=J|last5=Hudjashov|first5=G|last6=Kaldma|first6=K|last7=Serk|first7=P|last8=Karmin|first8=M|last9=Behar|first9=DM|last10=Gilbert|first10=M Thomas P|last11=Endicott|first11=Phillip|last12=Mastana|first12=Sarabjit|last13=Papiha|first13=Surinder S|last14=Skorecki|first14=Karl|last15=Torroni|first15=Antonio|last16=Villems|first16=Richard|volume=5|pages=26|pmc=516768|journal=BMC Genetics}} 2. ^{{Cite journal | doi=10.1186/s12862-016-0816-8| pmid=27832758| pmc=5105315|title = Carriers of human mitochondrial DNA macrohaplogroup M colonized India from southeastern Asia| journal=BMC Evolutionary Biology| volume=16| issue=1| pages=246|year = 2016|last1 = Marrero|first1 = Patricia| last2=Abu-Amero| first2=Khaled K.| last3=Larruga| first3=Jose M.| last4=Cabrera| first4=Vicente M.}} 3. ^{{cite journal | last1 = Quintana-Murci | first1 = Lluís | display-authors = etal | year = 1999 | title = Where West Meets East: The Complex mtDNA Landscape of the Southwest and Central Asian Corridor | url = | journal = Am. J. Hum. Genet. | volume = 74 | issue = 5| pages = 827–45 | doi=10.1086/383236| pmid = 15077202 | pmc = 1181978 }} 4. ^{{cite journal|title=Carriers of Mitochondrial DNA Macrohaplogroup N Lineages Reached Australia around 50,000 Years Ago following a Northern Asian Route |journal= PLOS ONE | pmc=4460043|pmid=26053380|doi=10.1371/journal.pone.0129839|volume=10|issue = 6|year=2015|page=e0129839 | last1 = Fregel | first1 = R | last2 = Cabrera | first2 = V | last3 = Larruga | first3 = JM | last4 = Abu-Amero | first4 = KK | last5 = González | first5 = AM}} 5. ^1 2 3 4 5 6 7 8 9 {{cite journal | last1 = Gonzalez | display-authors = etal | year = 2007 | title = Mitochondrial lineage M1 traces an early human backflow to Africa | journal = BMC Genomics | volume = 8 | issue = | page = 223 | doi = 10.1186/1471-2164-8-223 | pmc=1945034 | pmid=17620140}} 6. ^1 2 {{cite journal|last=Quintana|year=1999|url=http://www.clas.ufl.edu/users/krigbaum/proseminar/quintana-murci_naturegenetics_1999.pdf|title= Genetic evidence of an early exit of Homo sapiens sapiens from Africa through eastern Africa|display-authors=etal}} 7. ^{{cite journal|doi=10.3378/027.081.0407|title=Complete mitochondrial sequences for haplogroups M23 and M46: insights into the Asian ancestry of the Malagasy population|last=Dubut|year=2009|journal=Human Biology|pmid=20067372|first1=V|last2=Cartault|first2=F|last3=Payet|first3=C|last4=Thionville|first4=MD|last5=Murail|first5=P|volume=81|issue=4|pages=495–500|display-authors=etal}} 8. ^{{cite journal|title=A new deep branch of eurasian mtDNA macrohaplogroup M reveals additional complexity regarding the settlement of Madagascar|last=Ricaut|year=2009|doi=10.1186/1471-2164-10-605|journal=BMC Genomics|pmid=20003445|first1=FX|last2=Razafindrazaka|first2=H|last3=Cox|first3=MP|last4=Dugoujon|first4=JM|last5=Guitard|first5=E|last6=Sambo|first6=C|last7=Mormina|first7=M|last8=Mirazon-Lahr|first8=M|last9=Ludes|first9=B|last10=Crubézy|first10=Eric|volume=10|pages=605|pmc=2808327|display-authors=etal}} 9. ^1 2 3 4 5 6 7 {{cite journal | last1 = Rajkumar | display-authors = etal | year = 2005 | title = Phylogeny and antiquity of M macrohaplogroup inferred from complete mt DNA sequence of Indian specific lineages | journal = BMC Evolutionary Biology | volume = 5 | issue = | page = 26 | doi = 10.1186/1471-2148-5-26 | pmid=15804362 | pmc=1079809}} 10. ^1 {{cite journal | last1 = Maruyama | first1 = Sayaka | last2 = Minaguchi | first2 = Kiyoshi | last3 = Saitou | first3 = Naruya | year = 2003 | title = Sequence polymorphisms of the mitochondrial DNA control region and phylogenetic analysis of mtDNA lineages in the Japanese population | url = | journal = Int J Legal Med | volume = 117 | issue = 4| pages = 218–225 | doi = 10.1007/s00414-003-0379-2 | pmid = 12845447 }} 11. ^1 2 3 4 5 6 7 8 9 10 11 12 13 Thangaraj et al. (2006), In situ origin of deep rooting lineages of mitochondrial Macrohaplogroup 'M' in India, BMC Genomics 2006, 7:151 12. ^{{cite journal | last1 = Chandrasekar Adimoolam | first1 = Kumar S | last2 = Sreenath | first2 = J | last3 = Sarkar | first3 = BN | last4 = Urade | first4 = BP | display-authors = etal | year = 2009 | title = Updating Phylogeny of Mitochondrial DNA Macrohaplogroup M in India: Dispersal of Modern Human in South Asian Corridor | journal = PLoS ONE | volume = 4 | issue = 10| page = e7447 | doi = 10.1371/journal.pone.0007447 | pmid=19823670 | pmc=2757894}} 13. ^1 2 Olivieri et al. (2006), The mtDNA legacy of the Levantine early Upper Palaeolithic in Africa, Science. 2006 Dec 15;314(5806):1767-70 14. ^1 2 {{cite journal|last=Kivisild |year=2003|title=The Genetic Heritage of the Earliest Settlers Persists Both in Indian Tribal and Caste Populations|pmid=12536373|first1=T|last2=Rootsi|first2=S|last3=Metspalu|first3=M|last4=Mastana|first4=S|last5=Kaldma|first5=K|last6=Parik|first6=J|last7=Metspalu|first7=E|last8=Adojaan|first8=M|last9=Tolk|first9=HV|last10=Stepanov|first10=V.|last11=Gölge|first11=M.|last12=Usanga|first12=E.|last13=Papiha|first13=S.S.|last14=Cinnioğlu|first14=C.|last15=King|first15=R.|last16=Cavalli-Sforza|first16=L.|last17=Underhill|first17=P.A.|last18=Villems|first18=R.|volume=72|issue=2|pages=313–32|doi=10.1086/346068|pmc=379225|journal=American Journal of Human Genetics|display-authors=8}} 15. ^{{cite journal | last1 = Gonzalez | display-authors = etal | year = 2007 | title = Mitochondrial lineage M1 traces an early human backflow to Africa | journal = BMC Genomics | volume = 8 | issue = | page = 223 | doi = 10.1186/1471-2164-8-223 | pmc=1945034 | pmid=17620140}} 16. ^1 {{cite journal|last=Macaulay |title=Single, Rapid Coastal Settlement of Asia Revealed by Analysis of Complete Mitochondrial Genomes|year=2005|doi=10.1126/science.1109792|url=|pmid=15890885|first1=V|last2=Hill|first2=C|last3=Achilli|first3=A|last4=Rengo|first4=C|last5=Clarke|first5=D|last6=Meehan|first6=W|last7=Blackburn|first7=J|last8=Semino|first8=O|last9=Scozzari|first9=R|last10=Cruciani|first10=F|last11=Taha|first11=A|last12=Shaari|first12=N. K.|last13=Raja|first13=J. M.|last14=Ismail|first14=P|last15=Zainuddin|first15=Z|last16=Goodwin|first16=W|last17=Bulbeck|first17=D|last18=Bandelt|first18=H. J.|last19=Oppenheimer|first19=S|last20=Torroni|first20=A|last21=Richards|first21=M|volume=308|issue=5724|pages=1034–6|journal=Science|display-authors=8}}: "Haplogroup L3 (the African clade that gave rise to the two basal non-African clades, haplogroups M and N) is 84,000 years old, and haplogroups M and N themselves are almost identical in age at 63,000 years old, with haplogroup R diverging rapidly within haplogroup N 60,000 years ago." 17. ^{{cite journal|title=Revealing the prehistoric settlement of Australia by Y chromosome and mtDNA analysis|year=2007|pmid=17496137|doi=10.1073/pnas.0702928104|display-authors=8|last1=Hudjashov|first1=G|last2=Kivisild|first2=T|last3=Underhill|first3=PA|last4=Endicott|first4=P|last5=Sanchez|first5=JJ|last6=Lin|first6=AA|last7=Shen|first7=P|last8=Oefner|first8=P|last9=Renfrew|first9=C|last10=Villems|first10=R.|last11=Forster|first11=P.|volume=104|issue=21|pages=8726–30|pmc=1885570|journal=Proceedings of the National Academy of Sciences of the United States of America}} 18. ^1 {{cite journal|last=Abu-Amero|year=2008|title=Mitochondrial DNA structure in the Arabian Peninsula|doi=10.1186/1471-2148-8-45|pmid=18269758|first1=KK|last2=Larruga|first2=JM|last3=Cabrera|first3=VM|last4=González|first4=AM|volume=8|pages=45|pmc=2268671|journal=BMC Evolutionary Biology|display-authors=etal}} 19. ^{{cite journal | last1 = Ghezzi | display-authors = etal | year = 2005 | title = Mitochondrial DNA haplogroup K is associated with a lower risk of Parkinson's disease in Italians | journal = European Journal of Human Genetics | volume = 13 | issue = 6| pages = 748–752 | doi=10.1038/sj.ejhg.5201425 | pmid=15827561}} 20. ^1 2 3 4 5 {{cite journal | last1 = Umetsu | first1 = Kazuo | last2 = Tanaka | first2 = Masashi | last3 = Yuasa | first3 = Isao | display-authors = etal | year = 2005 | title = Multiplex amplified product-length polymorphism analysis of 36 mitochondrial single-nucleotide polymorphisms for haplogrouping of East Asian populations | url = | journal = Electrophoresis | volume = 26 | issue = 1| pages = 91–98 | doi=10.1002/elps.200406129| pmid = 15624129 }} 21. ^{{cite journal | last1 = Asari | first1 = Masaru | last2 = Umetsu | first2 = Kazuo | last3 = Adachi | first3 = Noboru | display-authors = etal | year = 2007 | title = ", "Utility of haplogroup determination for forensic mtDNA analysis in the Japanese population | url = | journal = Legal Medicine | volume = 9| issue = 5| pages = 237–240| doi = 10.1016/j.legalmed.2007.01.007 | pmid = 17467322 }} 22. ^1 2 3 4 5 6 7 {{ cite journal|last=Metspalu |title=Most of the extant mtDNA boundaries in South and Southwest Asia were likely shaped during the initial settlement of Eurasia by anatomically modern humans|doi=10.1186/1471-2156-5-26|pmid=15339343|year=2004|first1=M|last2=Kivisild|first2=T|last3=Metspalu|first3=E|last4=Parik|first4=J|last5=Hudjashov|first5=G|last6=Kaldma|first6=K|last7=Serk|first7=P|last8=Karmin|first8=M|last9=Behar|first9=DM|last10=Gilbert|first10=M Thomas P|last11=Endicott|first11=Phillip|last12=Mastana|first12=Sarabjit|last13=Papiha|first13=Surinder S|last14=Skorecki|first14=Karl|last15=Torroni|first15=Antonio|last16=Villems|first16=Richard|volume=5|pages=26|pmc=516768|journal=BMC Genetics|display-authors=etal}} 23. ^{{cite journal | last1 = Edwin | display-authors = etal | year = 2002 | title = Mitochondrial DNA diversity among five tribal populations of southern India | url = http://www.iisc.ernet.in/currsci/jul252002/158.pdf | journal = Current Science | volume = 83 | issue = | page = }} 24. ^{{cite journal | last1 = Kim | first1 = W | last2 = Yoo | first2 = T-K | last3 = Shin | first3 = D-J | last4 = Rho | first4 = H-W | last5 = Jin | first5 = H-J | display-authors = etal | year = 2008 | title = Mitochondrial DNA Haplogroup Analysis Reveals no Association between the Common Genetic Lineages and Prostate Cancer in the Korean Population | journal = PLoS ONE | volume = 3 | issue = 5| page = e2211 | doi = 10.1371/journal.pone.0002211 | pmid=18493608 | pmc=2376063}} 25. ^1 2 {{cite journal | last1 = Jin | first1 = H-J | last2 = Tyler-Smith | first2 = C | last3 = Kim | first3 = W | year = 2009 | title = The Peopling of Korea Revealed by Analyses of Mitochondrial DNA and Y-Chromosomal Markers | journal = PLoS ONE | volume = 4 | issue = 1| page = e4210 | doi = 10.1371/journal.pone.0004210 | pmid=19148289 | pmc=2615218}} 26. ^{{cite journal | last1 = Beom Hong | first1 = Seung | last2 = Cheol Kim | first2 = Ki | last3 = Kim | first3 = Wook | year = 2014 | title = Mitochondrial DNA haplogroups and homogeneity in the Korean population | url = | journal = Genes & Genomics | volume = 36| issue = 5| pages = 583–590| doi = 10.1007/s13258-014-0194-9 }} 27. ^1 {{cite journal | last1 = Peng | first1 = Min-Sheng | last2 = Ho Quang | first2 = Huy | last3 = Pham Dang | first3 = Khoa | display-authors = etal | year = 2010 | title = Tracing the Austronesian Footprint in Mainland Southeast Asia: A Perspective from Mitochondrial DNA | url = | journal = Mol. Biol. Evol. | volume = 27 | issue = 10| pages = 2417–2430 | doi = 10.1093/molbev/msq131 | pmid=20513740}} 28. ^1 {{cite journal | last1 = Bodner | first1 = Martin | last2 = Zimmermann | first2 = Bettina | last3 = Röck | first3 = Alexander | display-authors = etal | year = 2011 | title = Southeast Asian diversity: first insights into the complex mtDNA structure of Laos | journal = BMC Evolutionary Biology | volume = 11 | issue = | page = 49 | doi=10.1186/1471-2148-11-49 | pmid=21333001 | pmc=3050724}} 29. ^{{cite journal | last1 = Hudjashov | first1 = Georgi | last2 = Kivisild | first2 = Toomas | last3 = Underhill | first3 = Peter A. | display-authors = etal | year = 2007 | title = Revealing the prehistoric settlement of Australia by Y chromosome and mtDNA analysis | journal = PNAS | volume = 104 | issue = 21| pages = 8726–8730 | doi = 10.1073/pnas.0702928104 | pmid=17496137 | pmc=1885570}} 30. ^{{cite journal | last1 = Kayser | first1 = Manfred | last2 = Choi | first2 = Ying | last3 = van Oven | first3 = Mannis | display-authors = etal | title = ", (2008) "The Impact of the Austronesian Expansion: Evidence from mtDNA and Y Chromosome Diversity in the Admiralty Islands of Melanesia | url = | journal = Molecular Biology and Evolution | volume = 25 | issue = 7| pages = 1362–1374 | doi = 10.1093/molbev/msn078 | pmid = 18390477 | date=July 2008}} 31. ^{{cite journal | last1 = Shipley | first1 = G. P. | last2 = Taylor | first2 = D. A. | last3 = Tyagi | first3 = A. | last4 = Tiwari | first4 = G. | last5 = Redd | first5 = A. | year = 2015 | title = Genetic structure among Fijian island populations | url = | journal = Journal of Human Genetics | volume = 60 | issue = 2| pages = 69–75 | doi=10.1038/jhg.2014.105| pmid = 25566758 }} 32. ^{{cite web|last1=Non|first1=Amy|title=ANALYSES OF GENETIC DATA WITHIN AN INTERDISCIPLINARY FRAMEWORK TO INVESTIGATE RECENT HUMAN EVOLUTIONARY HISTORY AND COMPLEX DISEASE|url=http://etd.fcla.edu/UF/UFE0041981/non_a.pdf|publisher=University of Florida|accessdate=12 April 2016}} 33. ^{{cite web|last1=Holden|title=MtDNA variation in North, East, and Central African populations gives clues to a possible back-migration from the Middle East|url=http://konig.la.utk.edu/AJPA_Suppl_40_web.htm|publisher=American Association of Physical Anthropologists|accessdate=13 April 2016|deadurl=yes|archiveurl=https://web.archive.org/web/20160303212239/http://konig.la.utk.edu/AJPA_Suppl_40_web.htm|archivedate=3 March 2016|df=}} 34. ^{{cite journal|author1=Luísa Pereira |author2=Viktor Černý |author3=María Cerezo |author4=Nuno M Silva |author5=Martin Hájek |author6=Alžběta Vašíková |author7=Martina Kujanová |author8=Radim Brdička |author9=Antonio Salas |title=Linking the sub-Saharan and West Eurasian gene pools: maternal and paternal heritage of the Tuareg nomads from the African Sahel|journal=European Journal of Human Genetics|date=17 March 2010|volume=18|issue=8 |pages=915–923|doi=10.1038/ejhg.2010.21|pmid=20234393 |pmc=2987384}} 35. ^{{cite journal|vauthors=Witas HW, Tomczyk J, Jędrychowska-Dańska K, Chaubey G, Płoszaj T |title=mtDNA from the Early Bronze Age to the Roman Period Suggests a Genetic Link between the Indian Subcontinent and Mesopotamian Cradle of Civilization|journal=PLoS ONE|date=2013|volume=8|issue=9|doi=10.1371/journal.pone.0073682|pages=e73682|pmid=24040024|pmc=3770703}} 36. ^{{cite journal|author1=Cosimo Posth |author2=Gabriel Renaud |author3=Alissa Mittnik |author4=Dorothée G. Drucker |author5=Hélène Rougier |author6=Christophe Cupillard |author7=Frédérique Valentin |author8=Corinne Thevenet |author9=Anja Furtwängler |author10=Christoph Wißing |author11=Michael Francken |author12=Maria Malina |author13=Michael Bolus |author14=Martina Lari |author15=Elena Gigli |author16=Giulia Capecchi |author17=Isabelle Crevecoeur |author18=Cédric Beauval |author19=Damien Flas |author20=Mietje Germonpré |author21=Johannes van der Plicht |author22=Richard Cottiaux |author23=Bernard Gély |author24=Annamaria Ronchitelli |author25=Kurt Wehrberger |author26=Dan Grigorescu |author27=Jiří Svoboda |author28=Patrick Semal |author29=David Caramelli |author30=Hervé Bocherens |author31=Katerina Harvati |author32=Nicholas J. Conard |author33=Wolfgang Haak |author34=Adam Powell |title=Pleistocene Mitochondrial Genomes Suggest a Single Major Dispersal of Non-Africans and a Late Glacial Population Turnover in Europe|journal=Current Biology|date=March 21, 2016|volume=26|issue=6 |pages=827–833|doi=10.1016/j.cub.2016.01.037|url=http://www.cell.com/current-biology/abstract/S0960-9822%2816%2900087-7?_returnURL=http%3A%2F%2Flinkinghub.elsevier.com%2Fretrieve%2Fpii%2FS0960982216000877%3Fshowall%3Dtrue|accessdate=5 June 2016 |pmid=26853362}} 37. ^{{cite journal|author=van de Loosdrecht|display-authors=etal|title=Pleistocene North African genomes link Near Eastern and sub-Saharan African human populations|journal=Science|volume=360|issue=6388|pages=548–552|date=2018-03-15|issn=0036-8075|doi=10.1126/science.aar8380|pmid=29545507}} 38. ^{{cite biorxiv|author=Reyhan Yaka|title=Archaeogenetics of Late Iron Age Çemialo Sırtı, Batman: Investigating maternal genetic continuity in North Mesopotamia since the Neolithic|biorxiv=172890}} 39. ^{{cite journal|last1=Schuenemann, Verena J.|display-authors=etal|title=Ancient Egyptian mummy genomes suggest an increase of Sub-Saharan African ancestry in post-Roman periods|journal=Nature Communications|date=2017|volume=8|page=15694|pmid=28556824|doi=10.1038/ncomms15694|pmc=5459999}} 40. ^{{cite biorxiv|last1=Fregel|display-authors=etal|year=2018|title=Ancient genomes from North Africa evidence prehistoric migrations to the Maghreb from both the Levant and Europe|biorxiv=191569}} 41. ^{{cite journal|author=Konstantina Drosou |author2=Campbell Price |author3=Terence A. Brown|title=The kinship of two 12th Dynasty mummies revealed by ancient DNA sequencing|journal=Journal of Archaeological Science|date=February 2018|volume=17|pages=793–797|doi=10.1016/j.jasrep.2017.12.025}} 42. ^1 Kong, Qing-Peng et al 2010, Large-Scale mtDNA Screening Reveals a Surprising Matrilineal Complexity in East Asia and Its Implications to the Peopling of the Region 43. ^Hartmann et al. 2009, [https://archive.today/20120630045855/http://www3.interscience.wiley.com/journal/120756713/abstract?CRETRY=1&SRETRY=0 Validation of microarray-based resequencing of 93 worldwide mitochondrial genomes] 44. ^1 2 Derenko M, Malyarchuk B, Bahmanimehr A, Denisova G, Perkova M, et al. (2013), "Complete Mitochondrial DNA Diversity in Iranians." PLoS ONE 8(11): e80673. doi:10.1371/journal.pone.0080673 45. ^1 2 3 {{cite journal | last1 = Fornarino | first1 = Simona | last2 = Pala | first2 = Maria | last3 = Battaglia | first3 = Vincenza | display-authors = etal | year = 2009 | title = Mitochondrial and Y-chromosome diversity of the Tharus (Nepal): a reservoir of genetic variation | journal = BMC Evolutionary Biology | volume = 9 | issue = | page = 154 | doi = 10.1186/1471-2148-9-154 | pmid=19573232 | pmc=2720951}} 46. ^1 2 3 4 5 6 7 8 Chandrasekar A, Kumar S, Sreenath J, Sarkar BN, Urade BP, et al. (2009), "Updating Phylogeny of Mitochondrial DNA Macrohaplogroup M in India: Dispersal of Modern Human in South Asian Corridor. PLoS ONE 4(10): e7447. doi:10.1371/journal.pone.0007447 47. ^B. A. Malyarchuk, M. A. Perkova, M. V. Derenko, T. Vanecek, J. Lazur, and P. Gomolcak, "Mitochondrial DNA Variability in Slovaks, with Application to the Roma Origin." Annals of Human Genetics (2008) 72, 228–240. doi: 10.1111/j.1469-1809.2007.00410.x 48. ^{{cite journal | last1 = Peng | display-authors = etal | year = 2011 | title = Tracing the legacy of the early Hainan Islanders - a perspective from mitochondrial DNA| journal = BMC Evolutionary Biology | volume = 11 | issue = | page = 46 | doi = 10.1186/1471-2148-11-46 | pmid=21324107 | pmc=3048540}} 49. ^Rem I. Sukernik, Natalia V. Volodko, Ilya O. Mazunin, Nikolai P. Eltsov, Stanislav V. Dryomov, and Elena B. Starikovskaya, "Mitochondrial Genome Diversity in the Tubalar, Even, and Ulchi: Contribution to Prehistory of Native Siberians and Their Affinities to Native Americans." American Journal of Physical Anthropology 148:123–138 (2012). DOI 10.1002/ajpa.22050 50. ^Sardana A Fedorova, Maere Reidla, Ene Metspalu, et al., "Autosomal and uniparental portraits of the native populations of Sakha (Yakutia): implications for the peopling of Northeast Eurasia." BMC Evolutionary Biology 2013, 13:127. http://www.biomedcentral.com/1471-2148/13/127 51. ^1 2 3 4 5 6 7 8 9 Duggan AT, Whitten M, Wiebe V, Crawford M, Butthof A, et al. (2013), "Investigating the Prehistory of Tungusic Peoples of Siberia and the Amur-Ussuri Region with Complete mtDNA Genome Sequences and Y-chromosomal Markers." PLoS ONE 8(12): e83570. doi:10.1371/journal.pone.0083570 52. ^1 2 3 4 5 6 7 8 9 {{cite journal | last1 = Derenko | first1 = Miroslava | last2 = Malyarchuk | first2 = Boris | last3 = Grzybowski | first3 = Tomasz | display-authors = etal | year = 2007 | title = Phylogeographic Analysis of Mitochondrial DNA in Northern Asian Populations | journal = Am. J. Hum. Genet. | volume = 81 | issue = 5| pages = 1025–1041 | doi = 10.1086/522933 | pmid=17924343 | pmc=2265662}} 53. ^{{cite journal | last1 = Tanaka | first1 = Masashi | last2 = Cabrera | first2 = Vicente M. | last3 = González | first3 = Ana M. | display-authors = etal | date = October 2004 | title = Mitochondrial Genome Variation in Eastern Asia and the Peopling of Japan | journal = Genome Res. | volume = 14 | issue = 10| pages = 1832–1850 | doi = 10.1101/gr.2286304 | pmid = 15466285 | pmc=524407}} 54. ^1 2 3 4 5 6 7 8 9 10 11 12 Min-Sheng Peng, Weifang Xu, Jiao-Jiao Song, et al. (2017), "Mitochondrial genomes uncover the maternal history of the Pamir populations." European Journal of Human Genetics https://doi.org/10.1038/s41431-017-0028-8 55. ^1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 Behar et al., 2012b 56. ^{{cite journal |title=Early Austronesians: into and out of Taiwan |given1=Albert Min-Shan |surname1=Ko |given2=Chung-Yu |surname2=Chen |given3=Qiaomei |surname3=Fu |given4=Frederick |surname4=Delfin |given5=Mingkun |surname5=Li |given6=Hung-Lin |surname6=Chiu |given7=Mark |surname7=Stoneking |given8=Ying-Chin |surname8=Ko |journal=The American Journal of Human Genetics |volume=94 |issue=3 |pages=426–436 |year=2014 |doi=10.1016/j.ajhg.2014.02.003 |pmid=24607387 |pmc=3951936 }} 57. ^1 2 3 4 5 6 7 8 9 {{cite journal | last1 = Ji | first1 = Fuyun | last2 = Sharpley | first2 = Mark S. | last3 = Derbeneva | first3 = Olga | display-authors = etal | year = 2012| title = Mitochondrial DNA variant associated with Leber hereditary optic neuropathy and high-altitude Tibetans | journal = PNAS | volume = 109 | issue = 19| pages = 7391–7396 | doi = 10.1073/pnas.1202484109 | pmid=22517755 | pmc=3358837}} 58. ^{{cite journal | last1 = Yao | first1 = Yong-Gang | last2 = Kong | first2 = Qing-Peng | last3 = Wang | first3 = Cheng-Ye | display-authors = etal | year = 2004| title = Different Matrilineal Contributions to Genetic Structure of Ethnic Groups in the Silk Road Region in China | url = | journal = Mol. Biol. Evol. | volume = 21 | issue = 12| pages = 2265–2280 | doi = 10.1093/molbev/msh238 | pmid = 15317881 }} 59. ^{{cite journal | last1 = Derenko | first1 = M | last2 = Malyarchuk | first2 = B | last3 = Denisova | first3 = G | last4 = Perkova | first4 = M | last5 = Rogalla | first5 = U | display-authors = etal | year = 2012 | title = Complete Mitochondrial DNA Analysis of Eastern Eurasian Haplogroups Rarely Found in Populations of Northern Asia and Eastern Europe | journal = PLoS ONE | volume = 7 | issue = 2| page = e32179 | doi = 10.1371/journal.pone.0032179 | pmid=22363811 | pmc=3283723}} 60. ^Qing-Peng Kong, Hans-Jürgen Bandelt, Chang Sun, et al., "Updating the East Asian mtDNA phylogeny: a prerequisite for the identification of pathogenic mutations." Human Molecular Genetics, 2006, Vol. 15, No. 13 2076–2086. doi:10.1093/hmg/ddl130 61. ^{{cite journal | last1 = Fedorova | first1 = Sardana A | last2 = Reidla | first2 = Maere | last3 = Metspalu | first3 = Ene | display-authors = etal | year = 2013 | title = Autosomal and uniparental portraits of the native populations of Sakha (Yakutia): implications for the peopling of Northeast Eurasia | journal = BMC Evolutionary Biology | volume = 13 | issue = | page = 127 | doi=10.1186/1471-2148-13-127 | pmid=23782551 | pmc=3695835}} 62. ^1 {{cite journal | last1 = Tabbada | first1 = Kristina A. | last2 = Trejaut | first2 = Jean | last3 = Loo | first3 = Jun-Hun | display-authors = etal | title = Philippine Mitochondrial DNA Diversity: A Populated Viaduct between Taiwan and Indonesia? | url = | journal = Mol. Biol. Evol. | volume = 27 | issue = 1| pages = 21–31 | doi = 10.1093/molbev/msp215 | pmid=19755666 | date=Jan 2010}} 63. ^1 2 3 4 5 6 7 8 9 10 11 {{cite journal | last1 = Kutanan | first1 = Wibhu | last2 = Kampuansai | first2 = Jatupol | last3 = Changmai | first3 = Piya | display-authors = etal | year = 2018 | title = Contrasting maternal and paternal genetic variation of hunter-gatherer groups in Thailand | url = | journal = Scientific Reports | volume = 8 | issue = 1| page = 1536 | doi = 10.1038/s41598-018-20020-0 | pmid = 29367746 | pmc = 5784115 }} 64. ^1 2 {{cite journal | last1 = Scholes | first1 = Clarissa | last2 = Siddle | first2 = Katherine | last3 = Ducourneau | first3 = Axel | display-authors = etal | year = 2011 | title = Genetic Diversity and Evidence for Population Admixture in Batak Negritos from Palawan | url = | journal = American Journal of Physical Anthropology | volume = 146| issue = 1| pages = 62–72| doi = 10.1002/ajpa.21544 | pmid=21796613}} 65. ^1 2 3 {{cite journal | last1 = Zheng | first1 = H-X | last2 = Yan | first2 = S | last3 = Qin | first3 = Z-D | last4 = Wang | first4 = Y | last5 = Tan | first5 = J-Z | display-authors = etal | year = 2011 | title = Major Population Expansion of East Asians Began before Neolithic Time: Evidence of mtDNA Genomes | journal = PLoS ONE | volume = 6 | issue = 10| page = e25835 | doi = 10.1371/journal.pone.0025835 | pmid=21998705 | pmc=3188578}} 66. ^Malyarchuk, B. et al 2008c, [https://archive.today/20120630045858/http://www3.interscience.wiley.com/cgi-bin/fulltext/119387744/HTMLSTART Mitochondrial DNA Variability in Slovaks, with Application to the Roma Origin] 67. ^Comas et al. (2004), Admixture, migrations, and dispersals in Central Asia: evidence from maternal DNA lineages, European Journal of Human Genetics (2004) 12, 495–504. 68. ^1 {{cite journal|title=Updated comprehensive phylogenetic tree of global human mitochondrial DNA variation|journal=Human Mutation|year=2009|last=van Oven|volume=30|issue=2|pages=E386–E394|doi=10.1002/humu.20921|pmid=18853457|first1=M|last2=Kayser|first2=M|display-authors=etal}} External links
1 : Human mtDNA haplogroups |
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