Jump to content

Haplogroup C-M217

From Wikipedia, the free encyclopedia
(Redirected from Haplogroup C2 (Y-DNA))

Haplogroup C-M217
C2 (previously C3)[1]
Possible time of origin50,865 [95% CI 38,317 <-> 61,900] ybp[2]

52,500 or 44,900 ybp[3]

48,400 [95% CI 46,000 <-> 50,900] ybp[4]
Coalescence age35,383 [95% CI 25,943 <-> 44,092] ybp[2]

34,000 [95% CI 31,500 <-> 36,700] ybp[4]
Possible place of originProbably Central Asia or East Asia
AncestorC-M130
DescendantsC-M93 (C2a); C-CTS117 (C2b); C-P53.1 (C2c); C-P62 (C2d); C-F2613/Z1338 (C2e)
Defining mutationsM217, P44, PK2
Highest frequenciesOroqen 61%[5]-91%,[6] Evenks 12.9%[7] - 71%,[8][9] Ulchi 69%,[10] Nivkhs 38%[11]-71%,[12] Kazakhs 30%[13] (5.3% Ysty[13] - 80.3% Baiuly[13]),[14] Buryats 7%[15]-84%,[11] Evens 5%[9]-74%,[16] Mongolians 52.3%[16] (22.9% China,[17] 24.39% China,[18] 45% Northeast Mongolia,[19] 46.7% Oroqen Autonomous Banner,[5] 47.8% Southeast Mongolia,[19] 52.6% Northwest Mongolia,[19] 53.8% Batsümber,[5] 55% Central and Southwest Mongolia[19]), Tanana 42%,[20] Koryaks 33%[8][9]-48%,[12] Hazaras 35%[19]–40%,[21] Yukaghir 31%,[22] Daur 30.8%[5]-42.5%,[23] Sibe (Xinjiang) 26.8% (11/41)[5] - 29.5% (18/61),[24] Hezhe (Heilongjiang) 23%,[5][17] Manchu 17.67%[25] (9.3% Bijie[26] - 44.0% Heilongjiang[24]), Tujia ≈21% (16%,[27] 18% Jishou,[16] 21% Guizhou,[24] 23% Hubei,[24] 27% Hunan[28]), North Korean 23% (19%[citation needed]-27%[24]), Altai 22%[16]-24%,[6] Dong 21% (6% Guangxi,[24] 20% Hunan,[28] 22% Hunan,[24] 30% Guizhou[24]), Kyrgyz 20%[19]-26.6%,[29] Uzbeks 20% (Uzbekistan[6]) - 54% (Takhar[30]), Hani 18% (12% Mường Tè,[31] 18%,[5] 22% Yunnan[24]), South Korean 16% (11.6%-21%[citation needed]), Cheyenne 16%,[20] Apache 15%,[20] Northern Han 14.7% (4.3%-29.6%),[24] Tuvans 11%[32] – 15%,[22] Ainu 12.5%[11]-25%,[16] Hui 11%,[5][6] Sioux 11%,[20] Nogais 14%,[33] Crimean Tatars 9%,[33] Uyghurs 8.27% (0% Ürümqi,[5] 0% Turpan area,[24] 2.6% Keriya,[34] 3.1% Lopnur,[34] 6.0%,[16] 6.0% Ürümqi area,[24] 6.3% Bortala area,[24] 7.0% Yining area,[24] 7.7% Yili,[5] 8.37% Hetian area,[35] 11.8% Horiqol Township,[34] 16.08% Turpan area[35]), Vietnamese 7.6% (4.3%-12.5%[36]), Tajiks (Afghanistan) 7.6% (3.6%[30]-9.2%[19]), Southern Han 7.1% (0%-23.5%),[24] Tabassarans 7%[37]}, Abazinians 7%,[38] Japanese 5.9% (0% Tokyo,[39][40] Okinawa,[16] Aomori,[16] - 7.8% Fukuoka[41]), Adygei 2.9%,[37] Kabardians 2.4%,[37] Pashtuns 2.04%[30]

Haplogroup C-M217, also known as C2 (and previously as C3),[1] is a Y-chromosome DNA haplogroup. It is the most frequently occurring branch of the wider Haplogroup C (M130). It is found mostly in Central Asia, Eastern Siberia and significant frequencies in parts of East Asia and Southeast Asia including some populations in the Caucasus, Middle East, South Asia, East Europe. It is found in a much more widespread area with a low frequency of less than 2%.

The haplogroup C-M217 is now found at high frequencies among Central Asian peoples, indigenous Siberians, and some Native peoples of North America. In particular, males belonging to peoples such as the Buryats,[16][32] Evens,[16] Evenks,[16] Itelmens,[15] Tom Tatars,[42] Kalmyks,[32][43][44] Kazakhs, Koryaks,[15] Mongolians,[16][19] Negidals,[15] Nivkhs,[15] Udege,[15] and Ulchi[10] have high levels of M217.[6][16][45]

One particular haplotype within Haplogroup C2-M217 has received a great deal of attention, because of the possibility that it may represent direct patrilineal descent from Genghis Khan,[46] though that hypothesis is controversial. According to the recent result, C2's subgroups are divided into C2b and C2e, and in Mongolia, most belong to C2b(Genghis Khan modal), while very few are C2e. On the other hand, C2b takes minority and most are C2e in Japan and Korea and Southern East Asia. The specific subclade Haplogroup C3b2b1*-M401(xF5483) of the broader C-M48 subclade, which has been identified as a possible marker of the Manchu Aisin Gioro and has been found in ten different ethnic minorities in northern China, is totally absent from all Han Chinese populations (Heilongjiang, Gansu, Guangdong, Sichuan and Xinjiang).[47][48][49][50]

Y chromosome haplogroup C2c1a1a1-M407 is carried by Mongol descendants of the Northern Yuan ruler from 1474 to 1517, Dayan Khan, who is a male line descendant of Genghis Khan which was found out after geneticists in Mongolia conducted tests on them.
C2b1a3a1c2-F5481 clade of C2*-ST which is also widespread in Central Asia among Kazakhs, Hazaras and ordinary commoner Mongols.[51] The Kerey clan of the Kazakhs have a high amount of the C3* star-cluster (C2*-ST) Y chromosome and is very high among Hazaras, Kazakhs and Mongols in general.[52]

Toghan, Genghis Khan's sixth son has claimed descendants who have Y haplogroup C2b1a1b1-F1756 just like the first son of Genghis Khan, Jochi's descendants in the Kazakh Tore clan.[53]

Origin

[edit]

After sharing a most recent common ancestor with Haplogroup C-F3393 approximately 48,400 [95% CI 46,000 <-> 50,900] years before present,[2] Haplogroup C-M217 is believed to have begun spreading approximately 34,000 [95% CI 31,500 <-> 36,700] years before present[2] in eastern or central Asia.

The extremely broad distribution of Haplogroup C-M217 Y-chromosomes, coupled with the fact that the ancestral paragroup C is not found among any of the modern Siberian or North American populations among whom Haplogroup C-M217 predominates, makes the determination of the geographical origin of the defining M217 mutation exceedingly difficult. The presence of Haplogroup C-M217 at a low frequency but relatively high diversity throughout East Asia and parts of Southeast Asia makes that region one likely source. In addition, the C-M217 haplotypes found with high frequency among North Asian populations appear to belong to a different genealogical branch from the C-M217 haplotypes found with low frequency among East and Southeast Asians, which suggests that the marginal presence of C-M217 among modern East and Southeast Asian populations may not be due to recent admixture from Northeast or Central Asia.[54]

More precisely, haplogroup C2-M217 is now divided into two primary subclades: C2a-L1373 (sometimes called the "northern branch" of C2-M217) and C2b-F1067 (sometimes called the "southern branch" of C2-M217). The oldest sample with C2-M217 is AR19K in the Amur River basin (19,587-19,175 cal BP).[55]

C2a-L1373 (estimated TMRCA 16,000 [95% CI 14,300 <-> 17,800] ybp[4]) has been found often in populations from Central Asia through North Asia to the Americas, and rarely in individuals from some neighboring regions, such as Europe or East Asia. C2a-L1373 subsumes two subclades: C2a1-F3447 and C2a2-BY63635/MPB374. C2a1-F3447 includes all extant Eurasian members of C2a-L1373, whereas C2a2-BY63635/MPB374 contains extant South American members of C2a-L1373 as well as ancient archaeological specimens from South America and Chertovy Vorota Cave in Primorsky Krai. C2a1-F3447 (estimated TMRCA 16,000 [95% CI 14,700 <-> 17,400] ybp[4]) includes the Y-DNA of an approximately 14,000-year-old specimen from the Ust'-Kyakhta 3 site (located on the right bank of the Selenga River in Buryatia, near the present-day international border with Mongolia) and C2a1b-BY101096/ACT1942 (found in individuals from present-day Liaoning Province of China, South Korea, Japan, and a Nivkh from Russia) in addition to the expansive C2a1a-F1699 clade. C2a1a-F1699 (estimated TMRCA 14,000 [95% CI 12,700 <-> 15,300] ybp[4]) subsumes four subclades: C2a1a1-F3918, C2a1a2-M48, C2a1a3-M504, and C2a1a4-M8574. C2a1a1-F3918 subsumes C2a1a1a-P39, which has been found at high frequency in samples of some indigenous North American populations, and C2a1a1b-FGC28881, which is now found with varying (but generally quite low) frequency all over the Eurasian steppe, from Heilongjiang and Jiangsu in the east to Jihočeský kraj, Podlaskie Voivodeship, and Giresun in the west.[4] Haplogroup C2a1a2-M48 is especially frequent and diverse among present-day Tungusic peoples, but branches of it also constitute the most frequently observed Y-DNA haplogroup among present-day Mongols in Mongolia, Alshyns in western Kazakhstan, and Kalmyks in Kalmykia. Extant members of C2a1a3-M504 all share a relatively recent common ancestor (estimated TMRCA 3,900 [95% CI 3,000 <-> 4,800] ybp[4]), and they are found often among Mongols, Manchus (e.g. Aisin Gioro), Kazakhs (most tribes of the Senior Zhuz as well as the Kerei tribe of the Middle Zhuz), Kyrgyz, and Hazaras. C2a1a4-M8574 is sparsely attested and deeply bifurcated into C-Y176542, which has been observed in an individual from Ulsan and an individual from Japan,[4] and C-Y11990. C-Y11990 is likewise quite ancient (estimated TMRCA 9,300 [95% CI 7,900 <-> 10,700] ybp according to YFull[4] or 8,946 [99% CI 11,792 - 6,625] ybp according to FTDNA[56]) but rare, with one branch (C-Z22425) having been found sporadically in Jammu and Kashmir, Germany, and the United States and another branch (C-ZQ354/C-F8513) having been found sporadically in Slovakia (Prešov Region), China, Turkey, and Kipchak of the central steppe (Lisakovsk 23 Kipchak in Kazakhstan, medieval nomad from 920 ± 25 BP uncal or 1036 - 1206 CE).[4][56]

The predominantly East Asian distributed C-F1067 subsumes a major clade, C-F2613, and a minor clade, C-CTS4660. The minor clade C-CTS4660 has been found in China (including a Dai and several Han from southern China as well as a Han from Anhui and a Han from Inner Mongolia; according to Chinese genomics company 23mofang, C-CTS4660 is currently mainly concentrated in the Liangguang region of China, accounting for about 0.24% of the national male population[57]) and Thailand[56] (including Northern Thai and Lao Isan[58]). The major clade C-F2613 has known representatives from China (Oroqen,[59] Hezhe,[59] Manchu,[60] Uyghur,[60] Han, Tibetan,[60] Tujia,[59] Dai), Korea, Japan, Laos, Thailand, Vietnam, Bhutan, Bangladesh, Mongolia,[19][60] Kyrgyzstan (Dungan, Kyrgyz),[19] Tajikistan (Tajik[60]), Afghanistan (Hazara, Tajik),[19] Pakistan (Burusho, Hazara),[19] Nakhchivan, Chechnya, and Syria and includes the populous subclades C-F845, C-CTS2657, and C-Z8440. C-M407, a notable subclade of C-CTS2657, has expanded in a post-Neolithic time frame[61] to include large percentages of modern Buryat, Soyot, and Hamnigan males in Buryatia and Barghut males in Hulunbuir[62] in addition to many Kalmyks and other Mongols[32][43][19][63] and members of the Qongirat tribe in Kazakhstan[13] (but only 2 or 0.67% of a sample of 300 Korean males[64]).

The specific subclade haplogroup C3b2b1*-M401(xF5483)[65][66][67] has been identified as a possible marker of the Aisin Gioro and is found in ten different ethnic minorities in northern China, but completely absent from Han Chinese.[68][69][67]

Genetic testing also showed that the haplogroup C3b1a3a2-F8951 of the Aisin Gioro family came to southeastern Manchuria after migrating from their place of origin in the Amur river's middle reaches, originating from ancestors related to Daurs in the Transbaikal area. The Tungusic speaking peoples mostly have C3c-M48 as their subclade of C3 which drastically differs from the C3b1a3a2-F8951 haplogroup of the Aisin Gioro which originates from Mongolic speaking populations like the Daur. Jurchen (Manchus) are a Tungusic people. The Mongol Genghis Khan's haplogroup C3b1a3a1-F3796 (C3*-Star Cluster) is a fraternal "brother" branch of C3b1a3a2-F8951 haplogroup of the Aisin Gioro.[70] A genetic test was conducted on seven men who claimed Aisin Gioro descent with three of them showing documented genealogical information of all their ancestors up to Nurhaci. Three of them turned out to share the C3b2b1*-M401(xF5483) haplogroup, out of them, two of them were the ones who provided their documented family trees. The other four tested were unrelated.[71] The Daur Ao clan carries the unique haplogroup subclade C2b1a3a2-F8951, the same haplogroup as Aisin Gioro and both Ao and Aisin Gioro only diverged merely a couple of centuries ago from a shared common ancestor. Other members of the Ao clan carry haplogroups like N1c-M178, C2a1b-F845, C2b1a3a1-F3796 and C2b1a2-M48. People from northeast China, the Daur Ao clan and Aisin Gioro clan are the main carriers of haplogroup C2b1a3a2-F8951. The Mongolic C2*-Star Cluster (C2b1a3a1-F3796) haplogroup is a fraternal branch to Aisin Gioro's C2b1a3a2-F8951 haplogroup.[72]

Distribution

[edit]

Haplogroup C-M217 is the modal haplogroup among Mongolians and most indigenous populations of the Russian Far East, such as the Buryats, Northern Tungusic peoples, Nivkhs, Koryaks, and Itelmens. The subclade C-P39 is common among males of the indigenous North American peoples whose languages belong to the Na-Dené phylum. The frequency of Haplogroup C-M217 tends to be negatively correlated with distance from Mongolia and the Russian Far East, but it still comprises more than ten percent of the total Y-chromosome diversity among the Manchus, Koreans, Ainu, and some Turkic peoples of Central Asia. Beyond this range of high-to-moderate frequency, which contains mainly the northeast quadrant of Eurasia and the northwest quadrant of North America, Haplogroup C-M217 continues to be found at low frequencies, and it has even been found as far afield as Northwest Europe, Turkey, Pakistan, Bhutan,[73] Bangladesh,[4] Nepal[74] and adjacent regions of India,[75][76][77] Vietnam, Maritime Southeast Asia, and the Wayuu people of South America. It is found in Ossetians 4.7% (1/21),[37] and in Russians 0.73% (3/406),frequency ranges depending on the district.[32]), It's found 0.2% in Central/Southern Russia but 0.9% Rovslav and 0.7% Belgorod. It is found 0.5% in ethnic Bulgarians but 1.2% in Montana Province, 0.8% Sofia Province and 1.4% in an unknown area[78] some of whom exhibit divergent Y-STR haplotypes.[24] Haplogroup C-M127 also has been found with high frequency in a small sample of Uzbeks from Takhar, Afghanistan (7/13 = 54% C-M217[30]).

In an early study of Japanese Y-chromosomes, haplogroup C-M217 was found relatively frequently among Ainus (2/16=12.5%[11] or 1/4=25%[16]) and among Japanese of the Kyūshū region (8/104=7.7%[11]). However, in other samples of Japanese, the frequency of haplogroup C-M217 was found to be only about one to three percent.[11][5][16][39] In a study published in 2014, large samples of males from seven different Japanese cities were examined, and the frequency of C-M217 varied between a minimum of 5.0% (15/302 university students in Sapporo) and a maximum of 7.8% (8/102 adult males in Fukuoka), with a total of 6.1% (146/2390) of their sampled Japanese males belonging to this haplogroup; the authors noted that no marked geographical gradient was detected in the frequencies of haplogroups C-M217 or C-M8 in that study.[41]

The frequency of Haplogroup C-M217 in samples of Han from various areas has ranged from 0% (0/27) in a sample of Han from Guangxi[7] in southern China to 23.5% (4/17) in a sample of Han from Shanghai[7] in eastern China, 23.5% (8/34) in a sample of Han from Xi'an[36] in northwestern China, and 29.6% (8/27) in a sample of Han from Jilin[7] in northeastern China, with the frequency of this haplogroup in several studies' pools of all Han samples ranging between 6.0% and 12.0%.[5][6][16][11][24][36] C-M217 also has been found in many samples of ethnic minority populations from central and southern China, such as Dong (8/27 = 29.6% from Guizhou,[24] 10/45 = 22.2% from Hunan,[24] 1/17 = 5.9% from Guangxi[24]), Bulang (3/11 = 27.3% from Yunnan[24]), Tujia (6/26 = 23.1% from Hubei,[24] 7/33 = 21.2% from Guizhou,[24] 9/49 = 18.4% from Jishou, Hunan), Hani (13/60 = 21.7% from Yunnan,[24] 6/34 = 17.6%[5]), Yi (4/32 = 12.5% Boren from Yunnan,[24] 3/24 = 12.5% Yi from Sichuan,[24] 4/61 = 6.6% Yi from Yunnan[24]), Mulao (1/11 = 9.1% from Guangxi[24]), Naxi (1/12 = 8.3% from Yunnan[24]), Miao (7/92 = 7.6% from Guizhou,[24] 2/58 = 3.4%), Shui (2/29 = 6.9% from Guizhou[24]), She (3/47 = 6.4% from Fujian,[24] 1/34 = 2.9%[5]), Wa (1/16 = 6.3% from Yunnan[24]), Dai (1/18 = 5.6% from Yunnan[24]), Gelao (1/21 = 4.8% from Guizhou[24]), ethnic Vietnamese (2/45 = 4.4% from Guangxi[24]), Yao (1/28 = 3.6% from Guangdong,[24] 1/35 = 2.9% from Liannan, Guangdong,[5] 2/113 = 1.8% from Guangxi[24]), Bai (1/34 = 2.9% from Yunnan[24]), Tibetans (4/156 = 2.6%), Buyi (2/109 = 1.8% from Guizhou[24]), and Taiwanese aborigines (1/48 = 2.1%).[79][5][74]

In Vietnam, Y-DNA that belongs to haplogroup C-M217 has been found in about 7.5% of all published samples, including 12.5% (6/48) of a sample of Vietnamese from Hanoi, Vietnam,[36] 11.8% (9/76) of another sample of Kinh ("ethnic Vietnamese") from Hanoi, Vietnam, 10% (1/10) of a sample from Vietnam,[80] 8.5% (5/59) of a sample of Cham people from Binh Thuan, Vietnam, 8.3% (2/24) of another sample of Vietnamese from Hanoi,[81] 4.3% (3/70) of a sample of Vietnamese from an unspecified location in Vietnam,[79] 2.2% (1/46) of the KHV ("Kinh in Ho Chi Minh City, Vietnam") sample of the 1000 Genomes Project,[4][3] and 0% (0/27) of one study's samples of Kinh and Muong.[82] Macholdt et al. (2020) have found Y-DNA that belongs to haplogroup C-M217 in 4.67% (28/600) of a set of samples from Vietnam, including 26.8% (11/41) of a sample of Hmong from Điện Biên Phủ, 13.9% (5/36) of a sample of Pathen from Quang Bình District, 12.1% (4/33) of a sample of Hanhi from Mường Tè District, 10.3% (3/29) of a sample of Sila from Mường Tè District, and 10.0% (5/50) of a sample of Kinh (n=42 from Hanoi, including all five members of haplogroup C-M217).[31]

Haplogroup C-M217 has been found less frequently in other parts of Southeast Asia and nearby areas, including Myanmar (3/72 = 4.2% Bamar and Rakhine[83]), Laos (1/25 = 4.0% Lao from Luang Prabang), Malaysia (2/18 = 11.1% Malaysia,[80] 0/8 Malaysia,[81] 0/12 Malaysian (ordinary Malay near Kuala Lumpur),[11] 0/17 Orang Asli,[84] 0/27 Malay,[84] 0/32 Malaysia[79]), Java (1/37 = 2.7%, 1/141 = 0.71%[81]), Nepal (2/77 = 2.6% general population of Kathmandu), Thailand (1/40 = 2.5% Thai, mostly sampled in Chiang Mai;[36] 13/500 = 2.6% Northern Thailand, or 11/290 = 3.8% Northern Thai people and 2/91 = 2.2% Tai Lü[85]), the Philippines (1/48 = 2.1%, 1/64 = 1.6%), and Bali (1/641 = 0.2%).[74][79]

Although C-M217 is generally found with only low frequency (<5%) in Tibet and Nepal, there may be an island of relatively high frequency of this haplogroup in Meghalaya, India. The indigenous tribes of this state of Northeast India, where they comprise the majority of the local population, speak Khasian languages or Tibeto-Burman languages. A study published in 2007 found C-M217(xM93, P39, M86) Y-DNA in 8.5% (6/71) of a sample of Garos, who primarily inhabit the Garo Hills in the western half of Meghalaya, and in 7.6% (27/353) of a pool of samples of eight Khasian tribes from the eastern half of Meghalaya (6/18 = 33.3% Nongtrai from the West Khasi Hills, 10/60 = 16.7% Lyngngam from the West Khasi Hills, 2/29 = 6.9% War-Khasi from the East Khasi Hills, 3/44 = 6.8% Pnar from the Jaintia Hills, 1/19 = 5.3% War-Jaintia from the Jaintia Hills, 3/87 = 3.4% Khynriam from the East Khasi Hills, 2/64 = 3.1% Maram from the West Khasi Hills, and 0/32 Bhoi from Ri-Bhoi District).[76]

Subclade distribution

[edit]

The subclades of Haplogroup C-M217 with their defining mutation(s), according to the 2017 ISOGG tree:

Others

[edit]

P53.1 has been used in multiple studies, but at testing in the commercial labs it appears in too many parts of the Y tree, including multiple parts of haplogroup C. Listed 16 April 2016.

Phylogenetics

[edit]

Phylogenetic history

[edit]
Main article: Conversion table for Y chromosome haplogroups

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
C-M216 10 V 1F 16 Eu6 H1 C C* C C C C C C C C C C
C-M8 10 V 1F 19 Eu6 H1 C C1 C1 C1 C1 C1 C1 C1 C1 C1 C1 C1
C-M38 10 V 1F 16 Eu6 H1 C C2* C2 C2 C2 C2 C2 C2 C2 C2 C2 C2
C-P33 10 V 1F 18 Eu6 H1 C C2a C2a C2a1 C2a1 C2a C2a C2a1 C2a1 C2a1 removed removed
C-P44 10 V 1F 17 Eu6 H1 C C3* C3 C3 C3 C3 C3 C3 C3 C3 C3 C3
C-M93 10 V 1F 17 Eu6 H1 C C3a C3a C3a C3a C3a C3a C3a C3a C3a C3a C3a1
C-M208 10 V 1F 17 Eu6 H1 C C3b C2b C2a C2a C2b C2b C2a C2a C2a C2a C2a
C-M210 36 V 1F 17 Eu6 H1 C C3c C2c C4a C4a C4b C4b C4a C4a C4a C4a C4a

Phylogenetic trees

[edit]

See also

[edit]

Genetics

[edit]

Y-DNA C subclades

[edit]

Y-DNA backbone tree

[edit]

References

[edit]
  1. ^ a b ISOGG, 2015 "Y-DNA Haplogroup C and its Subclades – 2015" (15 September 2015).
  2. ^ a b c d e f g h i Monika Karmin, Lauri Saag, Mário Vicente, et al. (2015), "A recent bottleneck of Y chromosome diversity coincides with a global change in culture." Genome Research 25:1–8 Published by Cold Spring Harbor Laboratory Press; ISSN 1088-9051/15; http://www.genome.org/cgi/doi/10.1101/gr.186684.114.
  3. ^ a b Poznik GD, Xue Y, Mendez FL, 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.
  4. ^ a b c d e f g h i j k l m n o p q r s t u v w x y z aa ab ac ad ae af ag ah ai aj ak al am an ao ap aq ar as at au av aw ax ay az ba bb bc bd be bf bg bh bi bj bk bl bm bn bo bp bq br bs bt bu bv bw bx by bz ca cb cc cd ce cf cg ch ci cj ck cl cm cn co cp cq cr cs ct cu cv cw cx cy cz da db dc dd de df dg dh di dj dk dl dm dn do dp dq dr ds dt du dv dw dx dy dz ea eb ec ed ee ef eg eh ei ej ek el em en eo ep eq er es et eu ev ew ex ey ez fa fb fc fd fe ff fg fh fi fj fk fl fm fn fo fp fq fr fs ft fu fv fw fx fy fz ga gb gc gd ge gf YFull Haplogroup YTree v7.02.01 as of 15 March 2019
  5. ^ a b c d e f g h i j k l m n o p q Xue Y, Zerjal T, Bao W, et al. (April 2006). "Male demography in East Asia: a north-south contrast in human population expansion times". Genetics. 172 (4): 2431–9. doi:10.1534/genetics.105.054270. PMC 1456369. PMID 16489223.
  6. ^ a b c d e f Karafet T, Xu L, Du R, et al. (September 2001). "Paternal population history of East Asia: sources, patterns, and microevolutionary processes". Am. J. Hum. Genet. 69 (3): 615–28. doi:10.1086/323299. PMC 1235490. PMID 11481588.
  7. ^ a b c d Zhong H, Shi H, Qi XB, Duan ZY, Tan PP, Jin L, Su B, Ma RZ (January 2011). "Extended Y Chromosome Investigation Suggests Postglacial Migrations of Modern Humans into East Asia via the Northern Route". Molecular Biology and Evolution. 28 (1): 717–727. doi:10.1093/molbev/msq247. PMID 20837606.
  8. ^ a b Karafet TM, Osipova LP, Gubina MA, Posukh OL, Zegura SL, Hammer MF (December 2002). "High levels of Y-chromosome differentiation among native Siberian populations and the genetic signature of a boreal hunter-gatherer way of life". Hum. Biol. 74 (6): 761–89. doi:10.1353/hub.2003.0006. PMID 12617488. S2CID 9443804.
  9. ^ a b c Pakendorf B, Novgorodov IN, Osakovskij VL, Stoneking M (July 2007). "Mating patterns amongst Siberian reindeer herders: inferences from mtDNA and Y-chromosomal analyses". Am. J. Phys. Anthropol. 133 (3): 1013–27. doi:10.1002/ajpa.20590. PMID 17492671.
  10. ^ a b c d E. V. Balanovska, Y. V. Bogunov, E. N. Kamenshikova, et al., "Demographic and Genetic Portraits of the Ulchi Population." ISSN 1022-7954, Russian Journal of Genetics, 2018, Vol. 54, No. 10, pp. 1245–1253. doi:10.1134/S1022795418100046
  11. ^ a b c d e f g h i Tajima, Atsushi; Hayami, Masanori; Tokunaga, Katsushi; Juji, T; Matsuo, M; Marzuki, S; Omoto, K; Horai, S (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.
  12. ^ a b "KHARKOV, Vladimir Nikolaevich, "СТРУКТУРА И ФИЛОГЕОГРАФИЯ ГЕНОФОНДА КОРЕННОГО НАСЕЛЕНИЯ СИБИРИ ПО МАРКЕРАМ Y-ХРОМОСОМЫ," Genetika 03.02.07 and "АВТОРЕФЕРАТ диссертации на соискание учёной степени доктора биологических наук, Tomsk 2012" (PDF).
  13. ^ a b c d e f g h i E. E. Ashirbekov, D. M. Botbaev, A. M. Belkozhaev, A. O. Abayldaev, A. S. Neupokoeva, J. E. Mukhataev, B. Alzhanuly, D. A. Sharafutdinova, D. D. Mukushkina, M. B. Rakhymgozhin, A. K. Khanseitova, S. A. Limborska, and N. A. Aytkhozhina, "Distribution of Y-Chromosome Haplogroups of the Kazakh from the South Kazakhstan, Zhambyl, and Almaty Regions." Reports of the National Academy of Sciences of the Republic of Kazakhstan, ISSN 2224-5227, Volume 6, Number 316 (2017), 85 – 95.
  14. ^ Dulik MC, Osipova LP, Schurr TG (2011). "Y-chromosome variation in Altaian Kazakhs reveals a common paternal gene pool for Kazakhs and the influence of Mongolian expansions". PLOS ONE. 6 (3): e17548. Bibcode:2011PLoSO...617548D. doi:10.1371/journal.pone.0017548. PMC 3055870. PMID 21412412.
  15. ^ a b c d e f g h Lell JT, Sukernik RI, Starikovskaya YB, et al. (January 2002). "The dual origin and Siberian affinities of Native American Y chromosomes". Am. J. Hum. Genet. 70 (1): 192–206. doi:10.1086/338457. PMC 384887. PMID 11731934.
  16. ^ a b c d e f g h i j k l m n o p q Hammer MF, Karafet TM, Park H, et al. (2006). "Dual origins of the Japanese: common ground for hunter-gatherer and farmer Y chromosomes". J. Hum. Genet. 51 (1): 47–58. doi:10.1007/s10038-005-0322-0. PMID 16328082.
  17. ^ a b Guang‐Lin He, Meng‐Ge Wang, Xing Zou, Hui‐Yuan Yeh, Chang‐Hui Liu, Chao Liu, Gang Chen, and Chuan‐Chao Wang, "Extensive ethnolinguistic diversity at the crossroads of North China and South Siberia reflects multiple sources of genetic diversity." J. Syst. Evol. 00 (0): 1–21, 2022. doi: 10.1111/jse.12827
  18. ^ a b c d e f g h i j k l m n o p q r s t u v w x y z aa ab ac ad ae af ag ah ai aj ak al am an ao ap aq ar as at au av aw ax ay az ba bb bc bd be bf bg bh bi bj bk bl bm bn bo bp bq br bs bt bu bv bw bx by bz ca cb cc cd ce cf cg ch ci cj ck cl cm cn co cp cq cr cs ct cu cv cw cx cy cz da db dc dd de df dg dh di dj dk dl dm dn do dp dq dr ds dt du dv dw dx dy dz ea eb ec Phylogenetic tree of Haplogroup C2-M217 at 23mofang
  19. ^ a b c d e f g h i j k l m n o p q r s t u v Di Cristofaro J, Pennarun E, Mazières S, Myres NM, Lin AA, et al. (2013). "Afghan Hindu Kush: Where Eurasian Sub-Continent Gene Flows Converge". PLOS ONE. 8 (10): e76748. Bibcode:2013PLoSO...876748D. doi:10.1371/journal.pone.0076748. PMC 3799995. PMID 24204668.
  20. ^ a b c d e Zegura SL, Karafet TM, Zhivotovsky LA, Hammer MF (January 2004). "High-resolution SNPs and microsatellite haplotypes point to a single, recent entry of Native American Y chromosomes into the Americas". Mol. Biol. Evol. 21 (1): 164–75. doi:10.1093/molbev/msh009. PMID 14595095.
  21. ^ a b c d Sengupta S, Zhivotovsky LA, King R, 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". Am. J. Hum. Genet. 78 (2): 202–21. doi:10.1086/499411. PMC 1380230. PMID 16400607.
  22. ^ a b c Pakendorf B, Novgorodov IN, Osakovskij VL, Danilova AP, Protod'jakonov AP, Stoneking M (October 2006). "Investigating the effects of prehistoric migrations in Siberia: genetic variation and the origins of Yakuts". Hum. Genet. 120 (3): 334–53. doi:10.1007/s00439-006-0213-2. PMID 16845541. S2CID 31651899.
  23. ^ Wang Chi-zao，Shi Mei-sen, and Li Hui (2018), "The Origin of Daur from the Perspective of Molecular Anthropology" [分子人类学视野下的达斡尔族族源研究], Journal of North Minzu University (Philosophy and Social Science Edition) [北方民族大学学报(哲学社会科学版)], No. 5, Gen. No. 143.
  24. ^ a b c d e f g h i j k l m n o p q r s t u v w x y z aa ab ac ad ae af ag ah ai aj ak al am an ao ap Zhong, Hua; Shi, Hong; Xue-, XB; Qi, Bin; Jin, L; Ma, RZ; Su, B (2010). "Global distribution of Y-chromosome haplogroup C reveals the prehistoric migration routes of African exodus and early settlement in East Asia". Journal of Human Genetics. 55 (7): 428–35. doi:10.1038/jhg.2010.40. PMID 20448651.
  25. ^ A brief introduction to patrilineal haplogroups and national ancestry composition of the Manchu population in China by 23mofang (2021/1/21)
  26. ^ Chen J, He G, Ren Z, Wang Q, Liu Y, Zhang H, Yang M, Zhang H, Ji J, Zhao J, Guo J, Zhu K, Yang X, Wang R, Ma H, Wang C-C, and Huang J (2021), "Genomic Insights Into the Admixture History of Mongolic- and Tungusic-Speaking Populations From Southwestern East Asia." Front. Genet. 12:685285. doi: 10.3389/fgene.2021.685285
  27. ^ A brief introduction to the patrilineal haplogroups and national ancestry composition of the Tujia people in China by 23mofang (2021/1/21)
  28. ^ a b Xia, Zi-Yang; Yan, Shi; Wang, Chuan-Chao; et al. (2019), Inland-coastal bifurcation of southern East Asians revealed by Hmong-Mien genomic history, doi:10.1101/730903, S2CID 202028061
  29. ^ Guo, Y.; Xia, Z.; Cui, W.; Chen, C.; Jin, X.; Zhu, B. Joint Genetic Analyses of Mitochondrial and Y-Chromosome Molecular Markers for a Population from Northwest China. Genes 2020, 11, 564. doi:10.3390/genes11050564
  30. ^ a b c d e Haber, Marc; Platt, Daniel E.; Ashrafian Bonab, Maziar; Youhanna, Sonia C.; Soria-Hernanz, David F.; Martínez-Cruz, Begoña; Douaihy, Bouchra; Ghassibe-Sabbagh, Michella; et al. (28 March 2012). "Afghanistan's Ethnic Groups Share a Y-Chromosomal Heritage Structured by Historical Events". PLOS ONE. 7 (3): e34288. Bibcode:2012PLoSO...734288H. doi:10.1371/journal.pone.0034288. hdl:10230/23537. PMC 3314501. PMID 22470552.
  31. ^ a b c d e f g h i Enrico Macholdt, Leonardo Arias, Nguyen Thuy Duong, et al., "The paternal and maternal genetic history of Vietnamese populations." European Journal of Human Genetics (2020) 28:636–645. https://doi.org/10.1038/s41431-019-0557-4
  32. ^ a b c d e f Malyarchuk B, Derenko M, Denisova G, et al. (2010). "Phylogeography of the Y-chromosome haplogroup C in northern Eurasia". Annals of Human Genetics. 74 (6): 539–546. doi:10.1111/j.1469-1809.2010.00601.x. PMID 20726964. S2CID 40763875.
  33. ^ a b c Marchani EE, Watkins WS, Bulayeva K, Harpending HC, Jorde LB (2008). "Culture creates genetic structure in the Caucasus: autosomal, mitochondrial, and Y-chromosomal variation in Daghestan". BMC Genet. 9: 47. doi:10.1186/1471-2156-9-47. PMC 2488347. PMID 18637195.
  34. ^ a b c LIU Shuhu, NIZAM Yilihamu, RABIYAMU Bake, ABDUKERAM Bupatima, and DOLKUN Matyusup, "A study of genetic diversity of three isolated populations in Xinjiang using Y-SNP." Acta Anthropologica Sinica, 2018, 37(1): 146-156.
  35. ^ a b Lu Yan (2011), "Genetic Mixture of Populations in Western China." Shanghai: Fudan University, 2011: 1-84. (Doctoral dissertation in Chinese: 陆艳, "中国西部人群的遗传混合", 上海：复旦大学，2011: 1-84.)
  36. ^ a b c d e Kim SH, Kim KC, Shin DJ, et al. (2011). "High frequencies of Y-chromosome haplogroup O2b-SRY465 lineages in Korea: a genetic perspective on the peopling of Korea". Investig Genet. 2 (1): 10. doi:10.1186/2041-2223-2-10. PMC 3087676. PMID 21463511.
  37. ^ a b c d e Bayazit Yunusbayev, Mait Metspalu, Mari Järve, et al. (2012), "The Caucasus as an Asymmetric Semipermeable Barrier to Ancient Human Migrations." Molecular Biology and Evolution 29(1):359–365. doi:10.1093/molbev/msr221 Advance Access publication 13 September 2011.
  38. ^ a b Nasidze2004a
  39. ^ a b 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): 480–495. doi:10.1111/j.1469-1809.2006.00343.x. hdl:10130/491. PMID 17274803. S2CID 1041367.
  40. ^ a b Sae Naitoh, Iku Kasahara-Nonaka, Kiyoshi Minaguchi, and Phrabhakaran Nambiar, "Assignment of Y-chromosomal SNPs found in Japanese population to Y-chromosomal haplogroup tree." Journal of Human Genetics (2013) 58, 195–201; doi:10.1038/jhg.2012.159; published online 7 February 2013.
  41. ^ a b 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.
  42. ^ https://www.medgen-journal.ru/jour/article/view/2212/0?locale=en_US The structure of the gene pool of Tomsk Tatars according to Y-chromosome markers
  43. ^ a b Boris Malyarchuk, Miroslava Derenko, Galina Denisova, Sanj Khoyt, Marcin Wozniak, Tomasz Grzybowski, and Ilya Zakharov, "Y-chromosome diversity in the Kalmyks at the ethnical and tribal levels." Journal of Human Genetics (2013) 58, 804–811; doi:10.1038/jhg.2013.108; published online 17 October 2013.
  44. ^ a b c d e f g h i Natalia Balinova, Helen Post, Alena Kushniarevich, Siiri Rootsi, et al. (2019), "Y-chromosomal analysis of clan structure of Kalmyks, the only European Mongol people, and their relationship to Oirat-Mongols of Inner Asia." European Journal of Human Genetics. https://doi.org/10.1038/s41431-019-0399-0
  45. ^ a b Wells RS, Yuldasheva N, Ruzibakiev R, et al. (August 2001). "The Eurasian heartland: a continental perspective on Y-chromosome diversity". Proc. Natl. Acad. Sci. U.S.A. 98 (18): 10244–9. Bibcode:2001PNAS...9810244W. doi:10.1073/pnas.171305098. PMC 56946. PMID 11526236.
  46. ^ Zerjal T, Xue Y, Bertorelle G, et al. (March 2003). "The genetic legacy of the Mongols". Am. J. Hum. Genet. 72 (3): 717–21. doi:10.1086/367774. PMC 1180246. PMID 12592608. as PDF Archived 10 July 2012 at the Wayback Machine
  47. ^ Xue, Y; Zerjal, T; Bao, W; Zhu, S; Lim, SK; Shu, Q; Xu, J; Du, R; Fu, S; Li, P; Yang, H; Tyler-Smith, C (28 September 2015). "Recent Spread of a Y-Chromosomal Lineage in Northern China and Mongolia". Am. J. Hum. Genet. 77 (6): 1112–6. doi:10.1086/498583. PMC 1285168. PMID 16380921.
  48. ^ Xue, Y; Zerjal, T; Bao, W; Zhu, S; Lim, SK; Shu, Q; Xu, J; Du, R; Fu, S; Li, P; Yang, H; Tyler-Smith, C (2005). "Recent Spread of a Y-Chromosomal Lineage in Northern China and Mongolia". The American Journal of Human Genetics. 77 (6): 1112–1116. doi:10.1086/498583. PMC 1285168. PMID 16380921.
  49. ^ Xue, Y.; Zerjal, T.; Bao, W.; Zhu, S.; Lim, S. K.; Shu, Q.; Xu, J.; Du, R.; Fu, S.; Li, P.; Yang, H.; Tyler-Smith, C. (December 2005). "Recent Spread of a Y-Chromosomal Lineage in Northern China and Mongolia". Am J Hum Genet. 77 (6): 1112–1116. doi:10.1086/498583. PMC 1285168. PMID 16380921.
  50. ^ Yan, S.; Tachibana, H.; Wei, LH (2015). "Y chromosome of Aisin Gioro, the imperial house of the Qing dynasty". J Hum Genet. 60 (6): 295–298. arXiv:1412.6274. doi:10.1038/jhg.2015.28. PMID 25833470. S2CID 7505563.
  51. ^ Wei, Lan-Hai; Yan, Shi; Lu, Yan; Wen, Shao-Qing; Huang, Yun-Zhi; Wang, Ling-Xiang; Li, Shi-Lin; Yang, Ya-Jun; Wang, Xiao-Feng; Zhang, Chao; Xu, Shu-Hua; Yao, Da-Li; Jin, Li; Li, Hui (22 January 2018). "Whole-sequence analysis indicates that the Y chromosome C2*-Star Cluster traces back to ordinary Mongols, rather than Genghis Khan". European Journal of Human Genetics. 26 (2): 230–237. doi:10.1038/s41431-017-0012-3. PMC 5839053. PMID 29358612.
  52. ^ Abilev, Serikbai; Malyarchuk, Boris; Derenko, Miroslava; Wozniak, Marcin; Grzybowski, Tomasz; Zakharov, Ilya (2012). "The Y-chromosome C3* star-cluster attributed to Genghis Khan's descendants is present at high frequency in the Kerey clan from Kazakhstan". Human Biology. 84 (1, Article 12): 79–89. doi:10.3378/027.084.0106. PMID 22452430. S2CID 46684406.
  53. ^ Wen, Shao-Qing; Yao, Hong-Bing; Du, Pan-Xin; Wei, Lan-Hai; Tong, Xin-Zhu; Wang, Ling-Xiang; Wang, Chuan-Chao; Zhou, Bo-Yan; Shi, Mei-Sen; Zhabagin, Maxat; Wang, Jiucun (August 2019). "Molecular genealogy of Tusi Lu's family reveals their paternal relationship with Jochi, Genghis Khan's eldest son". Journal of Human Genetics. 64 (8): 815–820. doi:10.1038/s10038-019-0618-0. ISSN 1434-5161. PMID 31164702. S2CID 174810181.
  54. ^ Redd AJ, Roberts-Thomson J, Karafet T, et al. (April 2002). "Gene flow from the Indian subcontinent to Australia: evidence from the Y chromosome". Curr. Biol. 12 (8): 673–7. Bibcode:2002CBio...12..673R. doi:10.1016/S0960-9822(02)00789-3. PMID 11967156. S2CID 7752658. as PDF Archived 28 November 2007 at the Wayback Machine
  55. ^ Mao, Xiaowei; Zhang, Hucai; Qiao, Shiyu; Liu, Yichen; Chang, Fengqin; Xie, Ping; Zhang, Ming; Wang, Tianyi; Li, Mian; Cao, Peng; Yang, Ruowei; Liu, Feng; Dai, Qingyan; Feng, Xiaotian; Ping, Wanjing (June 2021). "The deep population history of northern East Asia from the Late Pleistocene to the Holocene". Cell. 184 (12): 3256–3266.e13. doi:10.1016/j.cell.2021.04.040. ISSN 0092-8674. PMID 34048699.
  56. ^ a b c d e f g h i j k l m n Haplogroup C-M217 on Discover by FamilyTreeDNA
  57. ^ "C-Cts4660单倍群详情".
  58. ^ Phylogenetic tree of Haplogroup O-F175 at TheYtree
  59. ^ a b c Lippold S, Xu H, Ko A, Li M, Renaud G, Butthof A, Schröder R, Stoneking M (2014). "Human paternal and maternal demographic histories: insights from high-resolution Y chromosome and mtDNA sequences". Investigative Genetics. 2014 (5): 13. doi:10.1186/2041-2223-5-13. PMC 4174254. PMID 25254093.
  60. ^ a b c d e Tatiana M. Karafet, Ludmila P. Osipova, Olga V. Savina, Brian Hallmark, and Michael F. Hammer (2018), "Siberian genetic diversity reveals complex origins of the Samoyedic-speaking populations." Am J Hum Biol. 2018;e23194. https://doi.org/10.1002/ajhb.23194. doi:10.1002/ajhb.23194
  61. ^ Yan S, Wang CC, Zheng HX, Wang W, Qin ZD, 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.
  62. ^ Boris A Malyarchuk, Miroslava Derenko, Galina Denisova, Marcin Woźniak, Urszula Rogalla, Irina Dambueva, and Tomasz Grzybowski, "Y chromosome haplotype diversity in Mongolic-speaking populations and gene conversion at the duplicated STR DYS385a,b in haplogroup C3-M407." Journal of Human Genetics (2016) 61, 491–496; doi:10.1038/jhg.2016.14; published online 25 February 2016.
  63. ^ V. N. Kharkov, K. V. Khamina, O. F. Medvedeva, K. V. Simonova, E. R. Eremina, and V. A. Stepanov, "Gene Pool of Buryats: Clinal Variability and Territorial Subdivision Based on Data of Y-Chromosome Markers." Russian Journal of Genetics, 2014, Vol. 50, No. 2, pp. 180–190. doi:10.1134/S1022795413110082
  64. ^ a b Park, Jin; Lee, Young; Kim, Young; -1#Myung, Hwan Na; et al. (2013). "Y-SNP miniplexes for East Asian Y-chromosomal haplogroup determination in degraded DNA". Forensic Science International: Genetics. 7 (1): 75–81. doi:10.1016/j.fsigen.2012.06.014. PMID 22818129.{{cite journal}}: CS1 maint: numeric names: authors list (link)
  65. ^ Wei, Ryan Lan-Hai; Yan, Shi; Yu, Ge; Huang, Yun-Zhi (November 2016). "Genetic trail for the early migrations of Aisin Gioro, the imperial house of the Qing dynasty". Journal of Human Genetics. 62 (3): 407–411. doi:10.1038/jhg.2016.142. PMID 27853133. S2CID 7685248.
  66. ^ Yan, Shi; Tachibana, Harumasa; Wei, Lan-Hai; Yu, Ge; Wen, Shao-Qing; Wang, Chuan-Chao (June 2015). "Y chromosome of Aisin Gioro, the imperial house of the Qing dynasty". Journal of Human Genetics. 60 (6): 295–8. arXiv:1412.6274. doi:10.1038/jhg.2015.28. PMID 25833470. S2CID 7505563.
  67. ^ a b "Did you know DNA was used to uncover the origin of the House of Aisin Gioro?". Did You Know DNA... 14 November 2016. Retrieved 5 November 2020.
  68. ^ Xue, Yali; Zerjal, Tatiana; Bao, Weidong; Zhu, Suling; Lim, Si-Keun; Shu, Qunfang; Xu, Jiujin; Du, Ruofu; Fu, Songbin; Li, Pu; Yang, Huanming; Tyler-Smith, Chris (2005). "Recent Spread of a Y-Chromosomal Lineage in Northern China and Mongolia". The American Journal of Human Genetics. 77 (6): 1112–1116. doi:10.1086/498583. PMC 1285168. PMID 16380921.
  69. ^ "Asian Ancestry based on Studies of Y-DNA Variation: Part 3. Recent demographics and ancestry of the male East Asians – Empires and Dynasties". Genebase Tutorials. Archived from the original on 25 November 2013.
  70. ^ Wei, Ryan Lan-Hai; Yan, Shi; Yu, Ge; Huang, Yun-Zhi (November 2016). "Genetic trail for the early migrations of Aisin Gioro, the imperial house of the Qing dynasty". Journal of Human Genetics. 62 (3). The Japan Society of Human Genetics: 407–411. doi:10.1038/jhg.2016.142. PMID 27853133. S2CID 7685248.
  71. ^ Yan, Shi; Tachibana, Harumasa; Wei, Lan-Hai; Yu, Ge; Wen, Shao-Qing; Wang, Chuan-Chao (June 2015). "Y chromosome of Aisin Gioro, the imperial house of the Qing dynasty". Journal of Human Genetics. 60 (6). Nature Publishing Group on behalf of the Japan Society of Human Genetics (Japan): 295–298. arXiv:1412.6274. doi:10.1038/jhg.2015.28. PMID 25833470. S2CID 7505563.
  72. ^ Wang, Chi-Zao; Wei, Lan-Hai; Wang, Ling-Xiang; Wen, Shao-Qing; Yu, Xue-Er; Shi, Mei-Sen; Li, Hui (August 2019). "Relating Clans Ao and Aisin Gioro from northeast China by whole Y-chromosome sequencing". Journal of Human Genetics. 64 (8). Japan Society of Human Genetics: 775–780. doi:10.1038/s10038-019-0622-4. PMID 31148597. S2CID 171094135.
  73. ^ a b Pille Hallast, Chiara Batini, Daniel Zadik, et al., "The Y-Chromosome Tree Bursts into Leaf: 13,000 High-Confidence SNPs Covering the Majority of Known Clades." Molecular Biology and Evolution doi:10.1093/molbev/msu327 Advance Access publication 2 December 2014.
  74. ^ a b c Gayden T, Cadenas AM, Regueiro M, et al. (May 2007). "The Himalayas as a directional barrier to gene flow". Am. J. Hum. Genet. 80 (5): 884–94. doi:10.1086/516757. PMC 1852741. PMID 17436243. 2/77=2.6% C-M217 in a sample of the general population of Kathmandu.
  75. ^ Fornarino S, Pala M, Battaglia V, et al. (2009). "Mitochondrial and Y-chromosome diversity of the Tharus (Nepal): a reservoir of genetic variation". BMC Evol. Biol. 9 (1): 154. Bibcode:2009BMCEE...9..154F. doi:10.1186/1471-2148-9-154. PMC 2720951. PMID 19573232. 1/26=3.8% C-M217 in a sample of Hindu Indians from the Terai.
  76. ^ a b Reddy BM, Langstieh BT, Kumar V, et al. (2007). "Austro-Asiatic tribes of Northeast India provide hitherto missing genetic link between South and Southeast Asia". PLOS ONE. 2 (11): e1141. Bibcode:2007PLoSO...2.1141R. doi:10.1371/journal.pone.0001141. PMC 2065843. PMID 17989774. Haplogroup C-M217 in 8.5% of a sample of 71 Garos and 7.7% of a pool of eight samples of Khasians totalling 353 individuals
  77. ^ Kivisild T, Rootsi S, Metspalu M, et al. (February 2003). "The genetic heritage of the earliest settlers persists both in Indian tribal and caste populations". Am. J. Hum. Genet. 72 (2): 313–32. doi:10.1086/346068. PMC 379225. PMID 12536373. C-M217 in 1/31=3.2% of a sample from West Bengal.
  78. ^ Y-Chromosome Diversity in Modern Bulgarians: New Clues about Their Ancestry, Karachanak S, Grugni V, Fornarino S, Nesheva D, Al-Zahery N, et al. (2013) Retrieved Oct 2013.
  79. ^ a b c d Karafet, Tatiana M.; Hallmark, Brian; Cox, Murray P.; et al. (2010). "Major East–West Division Underlies Y Chromosome Stratification across Indonesia". Mol. Biol. Evol. 27 (8): 1833–1844. doi:10.1093/molbev/msq063. PMID 20207712.
  80. ^ a b Kayser M, Brauer S, Cordaux R, Casto A, Lao O, Zhivotovsky LA, Moyse-Faurie C, Rutledge RB, Schiefenhoevel W, Gil D, Lin AA, Underhill PA, Oefner PJ, Trent RJ, Stoneking M (2006). "Melanesian and Asian Origins of Polynesians: mtDNA and Y Chromosome Gradients Across the Pacific". Molecular Biology and Evolution. 23 (11): 2234–2244. doi:10.1093/molbev/msl093. hdl:11858/00-001M-0000-0010-0145-0. PMID 16923821.
  81. ^ a b c Trejaut JA, Poloni ES, Yen JC, et al. (2014). "Taiwan Y-chromosomal DNA variation and its relationship with Island Southeast Asia". BMC Genetics. 15: 77. doi:10.1186/1471-2156-15-77. PMC 4083334. PMID 24965575.
  82. ^ Cai X, Qin Z, Wen B, Xu S, Wang Y, et al. (2011). "Human Migration through Bottlenecks from Southeast Asia into East Asia during Last Glacial Maximum Revealed by Y Chromosomes". PLOS ONE. 6 (8): e24282. Bibcode:2011PLoSO...624282C. doi:10.1371/journal.pone.0024282. PMC 3164178. PMID 21904623.
  83. ^ Peng MS, He JD, Fan L, Liu J, Adeola AC, Wu SF, et al. (August 2014). "Retrieving Y chromosomal haplogroup trees using GWAS data". European Journal of Human Genetics. 22 (8): 1046–50. doi:10.1038/ejhg.2013.272. PMC 4350590. PMID 24281365.
  84. ^ a b Bing Su, Li Jin, Peter Underhill, Jeremy Martinson, Nilmani Saha, Stephen T. McGarvey, Mark D. Shriver, Jiayou Chu, Peter Oefner, Ranajit Chakraborty, and Ranjan Deka, "Polynesian origins: Insights from the Y chromosome." PNAS (18 July 2000), vol. 97, no. 15, 8225–8228.
  85. ^ Brunelli A, Kampuansai J, Seielstad M, Lomthaisong K, Kangwanpong D, Ghirotto S, et al. (2017). "Y chromosomal evidence on the origin of northern Thai people". PLOS ONE. 12 (7): e0181935. Bibcode:2017PLoSO..1281935B. doi:10.1371/journal.pone.0181935. PMC 5524406. PMID 28742125.
  86. ^ Nasidze I, Quinque D, Dupanloup I, Cordaux R, Kokshunova L, Stoneking M (December 2005). "Genetic evidence for the Mongolian ancestry of Kalmyks". Am. J. Phys. Anthropol. 128 (4): 846–54. doi:10.1002/ajpa.20159. PMID 16028228.
  87. ^ a b c d e f g h i j k l m n o p q r s t u v w x y z aa ab ac ad ae af Phylogenetic tree of haplogroup C-M217 at TheYtree
  88. ^ a b c d e f g h i j k l m n o p q r s t u v w x y z aa ab ac ad ae af ag ah ai aj ak al am an ao ap aq ar as at au "FamilyTreeDNA – Genetic Testing for Ancestry, Family History & Genealogy". www.familytreedna.com.
  89. ^ a b Lan-Hai Wei, Yun-Zhi Huang, Shi Yan, et al., "Phylogeny of Y-chromosome haplogroup C3b-F1756, an important paternal lineage in Altaic-speaking populations." Journal of Human Genetics advance online publication, 1 June 2017; doi:10.1038/jhg.2017.60
  90. ^ "C-F3830 夏商东北大族". 祖源树. 2024. Retrieved 29 August 2024.
  91. ^ Khar'kov VN, Stepanov VA, Medvedev OF, et al. (2008). "[The origin of Yakuts: analysis of Y-chromosome haplotypes]". Mol. Biol. (Mosk.) (in Russian). 42 (2): 226–37. PMID 18610830.
  92. ^ a b Peter de Barros Damgaard, Nina Marchi, Simon Rasmussen, et al. (2018), "137 ancient human genomes from across the Eurasian steppes." Nature, volume 557, pages 369–374 (2018). https://doi.org/10.1038/s41586-018-0094-2
  93. ^ Lan-Hai Wei, Shi Yan, Ge Yu, et al. (2016), "Genetic trail for the early migrations of Aisin Gioro, the imperial house of the Qing dynasty." Journal of Human Genetics (2016), 1–5. doi:10.1038/jhg.2016.142
  94. ^ a b c d e f g h i Wibhu Kutanan, Jatupol Kampuansai, Metawee Srikummool, Andrea Brunelli, Silvia Ghirotto, Leonardo Arias, Enrico Macholdt, Alexander Hübner, Roland Schröder, and Mark Stoneking, "Contrasting Paternal and Maternal Genetic Histories of Thai and Lao Populations." Mol. Biol. Evol. Advance Access publication 12 April 2019. doi:10.1093/molbev/msz083
  95. ^ a b c d e f g h Wibhu Kutanan, Rasmi Shoocongdej, Metawee Srikummool, et al. (2020), "Cultural variation impacts paternal and maternal genetic lineages of the Hmong-Mien and Sino-Tibetan groups from Thailand." European Journal of Human Genetics. https://doi.org/10.1038/s41431-020-0693-x
  96. ^ "C-F5477单倍群详情".
  97. ^ "C-Mf10317单倍群详情".
  98. ^ Underhill PA, Shen P, Lin AA, et al. (November 2000). "Y chromosome sequence variation and the history of human populations". Nat. Genet. 26 (3): 358–61. doi:10.1038/81685. PMID 11062480. S2CID 12893406.
  99. ^ "C-Sk1037单倍群详情".
  100. ^ "C-Mf1020单倍群详情".
  101. ^ "C-Z45203单倍群详情".
[edit]
Retrieved from "https://en.wikipedia.org/w/index.php?title=Haplogroup_C-M217&oldid=1250261978"