Haplogroup C-M130

Haplogroup C
Possible time of origin	53,000 years BP [1]
Possible place of origin	Asia
Ancestor	CF
Descendants	C1 F3393/Z1426 (previously CxC3) C2 (previously C3*) M217.
Defining mutations	M130/RPS4Y711, P184, P255, P260

Haplogroup C is a major Y-chromosome haplogroup, defined by UEPs M130/RPS4Y711, P184, P255, and P260, which are all SNP mutations. One of two primary branches of Haplogroup CF alongside Haplogroup F. Haplogroup C is found in ancient populations on every continent except Africa and is the predominant Y-DNA haplogroup among males belonging to many peoples indigenous to Central Asia/Siberia, North America and Oceania.

In addition to the basal paragroup C*, this haplogroup now has two major branches: C1 (F3393/Z1426; previously CxC3, i.e. old C1, old C2, old C4, old C5 and old C6) and C2 (M217; the former C3).

Origins

Haplogroup C-M130 seems to have come into existence shortly after SNP mutation M168 occurred for the first time, bringing the modern Haplogroup CT into existence, from which Haplogroup CF, and in turn Haplogroup C, derived. This was probably at least 60,000 years before present. Although Haplogroup C-M130 attains its highest frequencies among the indigenous populations of Mongolia, the Russian Far East, Polynesia, Australia, and at moderate frequency in the Korean Peninsula and among the Manchus, it displays high diversity among modern populations of India. It is hypothesized that Haplogroup C-M130 either originated or underwent its longest period of evolution within India or the greater South Asian coastal region. The highest diversity is observed in Southeast Asia, and its northward expansion in East Asia started approximately 40,000 years ago.

It is believed to have migrated to the Americas some 6,000-8,000 years before present, and was carried by Na-Dené-speaking peoples into the northwest Pacific coast of North America. Asia, has another highly divergent lineage named haplogroup D which is related to haplogroup E , this proves (East) Asia has much genetic diversity. However, the distributions of Haplogroups C-M130 and D are entirely and utterly different, with various subtypes of Haplogroup C-M130 being found at high frequency among the Australian aborigines, Polynesians, Vietnamese, Kazakhs, Mongolians, Manchurians, Koreans, and indigenous inhabitants of the Russian Far East; and at moderate frequencies elsewhere throughout Asia and Oceania, including India and Southeast Asia; whereas Haplogroup D is found at high frequencies only among the Tibetans, Japanese peoples, and Andaman Islanders, and has been found neither in India nor among the aboriginal inhabitants of the Americas or Oceania.

Structure

C* (M130/Page51/RPS4Y711, M216)

• C1 (F3393)
  • C1a (CTS11043)
    • C1a1 M8
      • C1a1a P121
        • C1a1a1 CTS6678
        • C1a1a2 Z1356
    • C1a2 (previously C6) V20
      • C1a2a V222
      • C1a2b Z29329
  • C1b F1370
    • C1b1 K281
      • C1b1a B66/Z16458
        • C1b1a1 (previously C5) M356
        • C1b1a2 B65
    • C1b2 B477/Z31885
      • C1b2a (previously C2) M38
        • C1b2a1 M208
          • C1b2a1a P33
          • C1b2a1b P54
      • C1b2b (previously C4) M347
        • C1b2b1 M210
• C2 (previously C3) M217
  • C2a M93
  • C2b L1373, F1396
    • C2b1
      • C2b1a
        • C2b1a1
          • C2b1a1a P39
      • C2b1b (previously C3c) M48
  • C2c C-P53.1
  • C2d P62
  • C2e F2613/Z1338
    • C2e1
      • C2e1a
        • C2e1a1a M407
• Other, untaxonimised subclades:
  • C-P343: outside C1a1 (M8), C1b2a (M38), C1b1a1 (previously C5; M356), C1b2b (previously C4; M347), and C2 (ex-C3; M217), but its relation to other branches is not yet tested.
  • C-P55: outside C1b2a (M38), but its relation to other branches has not yet been verified, and;

(The above phylogenetic structure of haplogroup C-M130 subclades is based on the ISOGG 2015 tree, YCC 2008 tree and subsequent published research. )

Distribution

The distribution of Haplogroup C-M130 is generally limited to populations of northern Asia, eastern Asia, Oceania, and the Americas. There is a tendency for Haplogroup C-M130 to appear as the minor component of Y-chromosome diversity among a population in which the major component is accounted for by subclades of Haplogroup K (M9). Haplogroup C-M130 also rarely co-occurs alongside Haplogroup D, which is also common among populations of northern Eurasia. Due to the tremendous age of Haplogroup C, numerous secondary mutations have had time to accumulate, and many regionally important subbranches of Haplogroup C-M130 have been identified.

Basal paragroup C* is carried by up to 2.7% of indigenous Australian males, according to a 2015 study by Nagle et al. (That is, 1.0% of the Y-chromosomes of 657 individuals, before 56% of those samples were excluded as "non-indigenous".) C-M130* is also carried by smaller proportions of males from the Indian subcontinent, Sri Lanka and South East Asia. In Europe, it has also been found in males with the surname Llach originating from Garrotxa, Catalonia, Spain (but not males with the same surname from other areas). C* (M130) was also identified in prehistoric remains, dating from 34,000 years BP, found in Russia and known as "Kostenki 14".

C-M347 (C1b2b; previously known as C4) is the most common haplogroup amongst indigenous Australian males, was probably carried by approximately 43% of them before European settlement in Australia and it has not been found outside of that continent.

Haplogroup C-M217 – the most numerous and widely dispersed C lineage – which is believed to have originated in South East/Central Asia, spread from there into Northern Asia and the Americas. C-M130 stretches longitudinally from Central Europe and Turkey, to the Wayuu people of Colombia and Venezuela, and latitudinally from the Athabaskan peoples of Alaska to Vietnam to the Malay Archipelago. Found at low concentrations in Eastern Europe, where it may be a legacy of the invasions/migrations of the Huns, Turks and/or Mongols during the Middle Ages. Found at especially high frequencies in Buryats, Daurs, Hazaras, Itelmens, Kalmyks, Koryaks, Manchus, Mongolians, Oroqens, and Sibes, with a moderate distribution among other Tungusic peoples, Koreans, Ainus, Nivkhs, Altaians, Tuvinians, Uzbeks, Han Chinese, Tujia, Hani, and Hui. The highest frequencies of Haplogroup C-M217 are found among the populations of Mongolia and Far East Russia, where it is the modal haplogroup. Haplogroup C-M217 is the only variety of Haplogroup C-M130 to be found among Native Americans, among whom it reaches its highest frequency in Na-Dené populations.

Other subclades are specific to certain populations, within a restricted geographical range; even where these other branches are found, they tend to appear as a very low-frequency, minor component of the palette of Y-chromosome diversity within those territories:

• C-P33 (C1b2a1a ): found at high frequencies among Polynesian males.
• C-M8, an ancient but at present extremely rare lineage, is specific to the Japanese and Ryukyuan populations of Japan, among whom it occurs with a frequency of about 5%.
• C-M38 (C1b2a; previously C2), among some local populations within Indonesia, Melanesia (especially New Guinea), Micronesia, and some islands of Polynesia, C-M38 has become the modal haplogroup, probably due to severe founder effects and genetic drift.
• C-M356 has been detected with low frequency in samples from India, Nepal, Pakistan, Afghanistan, Arabia, and northern China.
• C-V20 (C1a2; previously C6) is found at low frequencies amongst Southern Europeans. The 7,000-year-old remains of a hunter-gatherer from La Braña, Asturias, Spain carried it, and C1a2 was also present in Hungary at around the same time.
• C-B66/Z16458 (C1b1a) is found at low frequencies in South Asia, Central Asia, and Southwest Asia.
• C-M93 (C2a) is found sporadically in Japanese people.
• C-M4 (C2b1b; previously C3c) is found at high frequencies in northern Tungusic peoples, Kazakhs, Oirats, Kalmyks, Mongolians, Yukaghirs, Nivkhs, Koryaks, Itelmens, and Udegeys, with a moderate distribution among southern Tungusic peoples, Buryats, Tuvinians, Yakuts, Chukchi, Kyrgyz, Uyghurs, Uzbeks, Karakalpaks, and Tajiks..
• C-P53.1 (C2c) is borne by about 10% of Xinjiang Sibe males, with low frequency in Mongolia and among Evenks, Ningxia Hui, Xizang Tibetan, Xinjiang Uyghur, and Gansu Han.
• C-P343 occurs at a high frequency among males from Lembata (17.4% of 92 samples), with lower frequencies in Flores, Pantar, and Timor. P343 is outside C1a1 (M8), C1b2a (M38), C2 (ex-C3; M217), C1b2b (previously C4; M347), or C1b1a1 (previously C5; M356), but its relation to other branches is not yet tested. It is outside C1a1 (M8), C1b2a (M38), C2 (ex-C3; M217), C1b2b (previously C4; M347), or C1b1a1 (previously C5; M356), but its relation to other branches is not yet tested.
• C-P55 is found in the New Guinea Highlands.
• C-L1373/F1396 (C2b) has been identified in Central Asia.
• C-P39 (C2b1a1a) is found among several indigenous peoples of North America, including some Na-Dené-, Algonquian- and Siouan-speaking populations.
• C-F2613/Z1338 (C2e): both Central Asia and East Asia.
• C-M407 (C2e1a1a) has been found at low frequencies in Bai, Cambodian, Han Chinese, Manchu, Tujia, Uyghur, and Yakut populations.
• Unspecified instances of C-130, which possibly belong to one of the above subclades, include:
  • C-RPS4Y (now C-RPS4Y711) (xM38) Y-DNA is quite common among populations of the Indonesian province of East Nusa Tenggara and independent East Timor: 13/31 = 41.9% Lembata, 16/71 = 22.5% Flores, 5/43 = 11.6% Solor, 10/96 = 10.4% Adonara, 3/39 = 7.7% East Timor, 1/26 = 3.8% Alor, 1/38 = 2.6% Pantar. All C-RPS4Y(xM38) individuals except the singleton from Alor were described as Austronesian speakers.
  • C-RPS4Y (now C-RPS4Y711) (xM38, M217) Y-DNA occurs, according to a study published in 2010, at rather high frequencies in most populations of central Indonesia (115/394 = 29.2% Flores, 21/92 = 22.8% Lembata, 19/86 = 22.1% Borneo, 6/54 = 11.1% Mandar, 1/9 = 11.1% Timor, but only 1/350 = 0.3% Sumba). C-RPS4Y(xM38, M217) Y-DNA generally becomes rare toward the west (2/61 = 3.3% Java, 1/32 = 3.1% Malaysia, 9/641 = 1.4% Balinese, 0/38 Batak Toba, 0/60 Nias, but 10/74 = 13.5% Mentawai) and toward the east (1/28 = 3.6% Alor, 0/30 Moluccas, 1/15 = 6.7% PNG Coast, 0/33 PNG Highland, 0/10 Nasioi, 0/44 Maewo (Vanuatu), 1/16 = 6.3% Micronesia, 0/64 Polynesia). C-RPS4Y711 (xM8, xM217) Y-DNA has also been found in 17% (6/35) of a sample of Yao from Bama, Guangxi in south-central China, 4/35 = 11% of a sample of Hui and 2/70 = 3% of a pair of samples of Uyghur from northwestern China, and 3/45 = 7% of a sample of Hezhe and 1/26 = 4% of a sample of Ewenki from northeastern China.
  • C-RPS4Y711 (xM8, M38, xM217) has been found in 48.5% (16/33) of a sample of indigenous Australians, 20% (12/60) of a sample of Yao, 6.1% (3/49) of a sample of Tujia, 5.9% (1/17) of a sample of Micronesians, 5.5% (3/55) of a sample of eastern Indonesians, 4.0% (1/25) of a sample of western Indonesians, 3.3% (3/91) of a sample of Sri Lankans, 3.1% (1/32) of a sample of Malays, 2.5% (10/405) of a sample of Indians, 2.2% (1/46) of a sample of Papua New Guineans, 1.7% (1/58) of a sample of Miao, and 1.5% (1/67) of a sample of Uyghurs.
  • "C-M216", an SNP that is now regarded as synonymous with C-M130 – xM8, M38, M217, M210, M356) have been found in 3.9% (3/77) of a sample of the general population of Kathmandu, Nepal. Other examples of C-M216 have been reported among Mongol and Turkic peoples, including the: Jalairs, Tatars, Kazakhs, Crimean Tatars, Merkits, Jochids and Uzbeks;

Phylogenetics

Phylogenetic history

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. 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

Research publications

The following research teams per their publications were represented in the creation of the YCC Tree.

3

Notable members

One particular haplotype within Haplogroup C-M217 has received a great deal of attention for the possibility that it may represent direct patrilineal descent from Genghis Khan.

See also

Genetics

3

Y-DNA C Subclades

3

Y-DNA backbone tree

Evolutionary tree of human Y-chromosome DNA haplogroups
	"Y-chromosomal Adam"
		A00	A0-T
			A0	A1
				A1a	A1b
					A1b1		BT
						B	CT
							DE						CF
						D	E		C		F
															F1	F2		F3	GHIJK
																				G	HIJK
																						H	IJK
																							IJ	K
																						I	J		LT		K2
																										L	T		NO	K2b	K2c	K2d		K2e
																													N	O		K2b1	P
																																	M	S		Q	R
Y-DNA by populations Famous Y-DNA haplotypes

External links

• C3-M217 FTDNA
• Spread of Haplogroup C, from National Geographic
• https://groups.google.com/forum/#!topic/mintamil/k1GofGgPfXY

Evolutionary tree of human Y-chromosome DNA haplogroups
	"Y-chromosomal Adam"
		A00	A0-T
			A0	A1
				A1a	A1b
					A1b1		BT
						B	CT
							DE						CF
						D	E		C		F
															F1	F2		F3	GHIJK
																				G	HIJK
																						H	IJK
																							IJ	K
																						I	J		LT		K2
																										L	T		NO	K2b	K2c	K2d		K2e
																													N	O		K2b1	P
																																	M	S		Q	R
Y-DNA by populations Famous Y-DNA haplotypes