Haplogroup C-F3393

Haplogroup C1 also known as C-F3393, is a major Y-chromosome haplogroup. It is one of two primary branches of the broader Haplogroup C, the other being C2 (also known as C-M217; the former Haplogroup C3).

Haplogroup C1 F3393
Possible time of originabout 49,200 years ago[1]
Possible place of originSouth West Asia[2]
AncestorHaplogroup C
DescendantsC1a CTS11043 (C1a1 M8; C1a2 (previously C6) V20)
C1b1a B66/Z16458; C1b1a1 M356 (previously C5)
C1b2 C-B477 (C1b2a M38 (previously C2); C1b2a1a P33; C1b2b (previously C4) M347)
Defining mutationsF3393

The basal paragroup, C1* (C-F3393*), has not been found in samples from living or dead males.

Of the two primary branches, C1b is common in parts of Oceania and Asia. The other primary branch, C1a, is extremely rare worldwide and has been found mainly amongst individuals native to Japan or Europe and among Upper Paleolithic Europeans, with single cases known from Nepal and Jeju Island through academic studies and from an ethnic Armenian, an ethnic Kabyle, and an ethnic Han from Liaoning province of China through commercial testing.

Distribution
Migration of Haplogroup C (Y-DNA)

Subclades of C1 (C-F3393) are the predominant Y-DNA haplogroups among some Indigenous Australian peoples, some Pacific Islander peoples, and a few of the ethnic groups of the Lesser Sunda Islands of Indonesia. Other subclades are found, at very low frequencies, in isolated locations throughout the Eurasian landmass and adjoining islands.

C1a (CTS11043)

Basal C1a* (CTS11043) was found in an Upper Paleolithic Europeans (Aurignacians), GoyetQ116-1 and Pestera Muerii2.[3]

Among the most interesting findings of recent genetic research is that living members of C1a are also rare and distributed geographically in an extremely bifurcated pattern.

C1a1 or C-M8 is now found regularly only with low frequency (approximately 5% of all samples) in Japan.[4]

C1a2 (known previously as C6) or C-V20 now appears to be found only among European, Kabyle, Armenian, and Nepali males.[5][6]

C1a2 was present in the remains in Europe by the Upper Paleolithic, including the Vestonice cluster (Vestonice16) (i.e. remains found in the modern Czech Republic). It was also found in the 7,000-year-old (Mesolithic) remains of a WHG (Western Hunter-Gatherers) known as "La Braña 1", found in La Braña-Arintero, León, Spain.[7] La Braña 1 was part of the so-called Villabruna cluster, named after a site in northeast Italy. By the time of the Villabruna cluster, however, the dominant Y-DNA haplogroup in Western Europe was I2. (And the balance was again altered by the mass migrations into Europe of Neolithic Middle Eastern farmer and Bronze Age Indo-Europeans.)[8][9] further: a male from the Great Hungarian Plain, approximately contemporaneous to the La Braña man also carried it,[4][10] as did the 30,000-year-old remains of a Vestonice Cluster hunter-gatherer from the Pavlov-Dolní Věstonice area (Czech Republic),[11] as well as a 34,000 years old Russian hunter gatherers from Sungir (Sunghir 1/2/3/4).[12]

C1b (F1370)

Basal C1b* (F1370) has been identified in the remains of an individual known as Kostenki-14 who died circa 37,000 years BP (Upper Paleolithic) that was found at the Kostyonki archaeological site in western Russia. It has also been found in a small number of males from the Middle East.[13]

C1b2 (C-B477) is the common ancestor of C-M38 and C-M347.

It is likely that more than 40% of Indigenous Australian males, before contact with European settlers, belonged to the subclade C1b2b (C-M347) known previously as C4.[14] Within C-M347 at least two subclades have been identified: C1b2b1 (DYS390.1del,M210) and an as yet unresolved offshoot of the C1b2b1 paragroup (i.e. M347xDYS390.1del,M210).

C1b2a (M38), previously known as C2, is virtually restricted to Island South East Asia, New Guinea, Melanesia, and Polynesia.[4] Of its subclades, C1b2a1a (P33) is found at a high frequency among Polynesians.[15][16]

Some members of populations in parts of Asia have been found to carry Y-DNA that belongs to haplogroup C1b1-AM00694/K281. C1b1b-B68 has been found in a Dusun in Brunei.[17] C1b1a-B66/Z16458 has three primary subclades: C1b1a1-M356, C1b1a2-B65, and C1b1a3-Z16582. C1b1a3-Z16582 has been found in some individuals from Saudi Arabia and Iraq. C1b1a2-B65 comprises two subclades, C1b1a2a-B67 and C1b1a2b-F725. C1b1a2a-B67 has been found in two Lebbo' people in Borneo, Indonesia.[17] C1b1a2b-F725 has been found in Han Chinese in China (Guangdong, Hunan, and Shaanxi), Dai people in Yunnan, Murut people in Brunei,[17] Malay people in Singapore,[17] and Aeta people in the Philippines.[17] C1b1a1-M356 has been found with overall low frequency in South Asia, Central Asia, and Southwest Asia.[18][19][20][21][22][23]

Phylogenetic structure
  • C1 F3393
    • C1a CTS11043
      • C1a1 M8
        • C1a1a P121
          • C1a1a1 CTS9336
            • C1a1a1a CTS6678 Japan, South Korea
            • C1a1a1b Z1356 Japan
          • C1a1a2 Z45460 China (Liaoning)
      • C1a2 (previously C6) V20
        • C1a2a V182
          • C1a2a1 V222 United Kingdom, Italy (Calabria), Greece, Hungary, Ukraine
            • C-Y12152 Scotland
              • C-BY1117 Hungary, England
              • C-Y11695 Italy, Greece, Ukraine
            • C-BY67541 Italy, Germany
          • C1a2a2 Z29329 Spain, Poland
        • C1a2b Z38888/F16270/PH428 Lithuania, Ireland, England, Algeria, Armenians
          • C-Z44576 Algeria
          • C-Z44526/F15182 England, Armenian
    • C1b F1370
      • C1b1 K281
        • C1b1a B66/Z16458
          • C1b1a1 (previously C5) M356 India, Sri Lanka, Bangladesh, Nepal, Pakistan, Afghanistan,[24] Iran, United Arab Emirates, Kuwait, Saudi Arabia, China (Xinjiang & Shanxi), Myanmar,[25] Thailand[26]
          • C1b1a2 B65 Borneo, China (Yunnan, Guangdong, Hunan, Shaanxi), Singapore, the Philippines
          • C1b1a3 Z16582 Saudi Arabia, Iraq
        • C1b1b B68 Borneo
      • C1b2 B477/Z31885
        • C1b2a (previously C2) M38
          • C1b2a1 M208
            • C1b2a1a P33 Polynesia
            • C1b2a1b P54
        • C1b2b (previously C4) M347 Australia
          • C1b2b1 M210

See also
Phylogenetic tree of human Y-chromosome DNA haplogroups [χ 1][χ 2]
"Y-chromosomal Adam"
A00 A0-T [χ 3]
A0 A1 [χ 4]
A1a A1b
A1b1 BT
B CT
DE CF
D E C F
F1  F2  F3  GHIJK
G HIJK
IJK H
IJ K
I   J     LT [χ 5]       K2 [χ 6]
L     T    K2a [χ 7]        K2b [χ 8]     K2c     K2d K2e [χ 9]  
K-M2313 [χ 10]     K2b1 [χ 11] P [χ 12]
NO   S [χ 13]  M [χ 14]    P1     P2
N O Q R

Footnotes
  1. C-F3393 tree, Yfull
  2. 崎谷満『DNA・考古・言語の学際研究が示す新・日本列島史』（勉誠出版　2009年）(in Japanese)
  3. Fu, Q.; Posth, C.; Hajdinjak, M.; Petr, M.; Mallick, S.; Fernandes, D.; Furtwängler, A.; Haak, W.; Meyer, M.; Mittnik, A.; Nickel, B.; Peltzer, A.; Rohland, N.; Slon, V.; Talamo, S.; Lazaridis, I.; Lipson, M.; Mathieson, I.; Schiffels, S.; Skoglund, P.; Derevianko, A. P.; Drozdov, N.; Slavinsky, V.; Tsybankov, A.; Cremonesi, R. G.; Mallegni, F.; Gély, B.; Vacca, E.; González Morales, M. R.; et al. (2016). "The genetic history of Ice Age Europe". Nature. 534 (7606): 200–205. Bibcode:2016Natur.534..200F. doi:10.1038/nature17993. PMC 4943878. PMID 27135931.
  4. ISOGG, 2015 "Y-DNA Haplogroup C and its Subclades – 2015" (15 September 2015).
  5. Scozzari R, Massaia A, D'Atanasio E, Myres NM, Perego UA, Trombetta B, Cruciani F (202). "Molecular dissection of the basal clades in the human Y chromosome phylogenetic tree". PLOS ONE. 7 (11): e49170. Bibcode:2012PLoSO...749170S. doi:10.1371/journal.pone.0049170. PMC 3492319. PMID 23145109.
  6. Hallast P, Batini C, Zadik D, Maisano Delser P, Wetton JH, Arroyo-Pardo E, et al. (March 2015). "The Y-chromosome tree bursts into leaf: 13,000 high-confidence SNPs covering the majority of known clades". Molecular Biology and Evolution. 32 (3): 661–73. doi:10.1093/molbev/msu327. PMC 4327154. PMID 25468874.
  7. http://dienekes.blogspot.ru/2014/01/brown-skinned-blue-eyed-y-haplogroup-c.html%5B%5D
  8. Gibbons, Ann (2017). "There's no such thing as a 'pure' European—or anyone else". Science. doi:10.1126/science.aal1186.
  9. Siska V, Jones ER, Jeon S, Bhak Y, Kim HM, Cho YS, Kim H, Lee K, Veselovskaya E, Balueva T, Gallego-Llorente M, Hofreiter M, Bradley DG, Eriksson A, Pinhasi R, Bhak J, Manica A (February 2017). "Genome-wide data from two early Neolithic East Asian individuals dating to 7700 years ago". Science Advances. 3 (2): e1601877. Bibcode:2017SciA....3E1877S. doi:10.1126/sciadv.1601877. PMC 5287702. PMID 28164156. Lay summary – University of Cambridge Research (February 1, 2017).
  10. Haak W, Lazaridis I, Patterson N, Rohland N, Mallick S, Llamas B, et al. (June 2015). "Massive migration from the steppe was a source for Indo-European languages in Europe". Nature. 522 (7555): 207–11. arXiv:1502.02783. Bibcode:2015Natur.522..207H. doi:10.1038/nature14317. PMC 5048219. PMID 25731166.
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  12. Sikora M, Seguin-Orlando A, Sousa VC, Albrechtsen A, Korneliussen T, Ko A, et al. (November 2017). "Ancient genomes show social and reproductive behavior of early Upper Paleolithic foragers". Science. 358 (6363): 659–662. Bibcode:2017Sci...358..659S. doi:10.1126/science.aao1807. PMID 28982795.
  13. https://sites.google.com/site/haplogroupcproject/%5B%5D
  14. Hudjashov G, Kivisild T, Underhill PA, Endicott P, Sanchez JJ, Lin AA, Shen P, Oefner P, Renfrew C, Villems R, Forster P (May 2007). "Revealing the prehistoric settlement of Australia by Y chromosome and mtDNA analysis". Proceedings of the National Academy of Sciences of the United States of America. 104 (21): 8726–30. Bibcode:2007PNAS..104.8726H. doi:10.1073/pnas.0702928104. PMC 1885570. PMID 17496137.
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  16. Cox MP, Redd AJ, Karafet TM, Ponder CA, Lansing S, Sudoyo H, Hammer MF (October 2007). "A Polynesian motif on the Y chromosome: population structure in remote Oceania". Human Biology. 79 (5): 525–35. doi:10.1353/hub.2008.0004. hdl:1808/13585. PMID 18478968. S2CID 4834817.
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