Haplogroup NO1

Last updated
Haplogroup NO1
Haplogroup NO.png
Possible time of originFormed circa 45,400–45,840 years  BP
(NO/NO1, based on YFull 2017, [1] and previous estimates of: 41,500 [95% CI 37,400 <-> 45,600] years BP, [2] 48,871 [95% CI 37,095 <-> 58,831] years BP, [3] and 50,800 or 43,500 years BP [4] )
Coalescence ageCirca 41,500 – 40,067 years BP (NO/NO1, based on YFull 2017, [1] and previous estimates of: 36,800 [95% CI 34,300 <-> 39,300] years BP, [2] 41,900 [31,294 <-> 51,202] years BP, [3] and 44,700 or 38,300 years BP depending on mutation rate [4] )
Possible place of origin Southeast Asia or East Asia (Northern China) [5] [6] [7]
Ancestor K-M2313 (M2313/Z4858)
Descendants N (M231) and O (M175). [8]
Defining mutationsM214/Page39; F176/M2314; CTS5858/M2325/F346; CTS11572 [1] [6]

Haplogroup NO1 (M214/Page39; F176/M2314; CTS5858/M2325/F346; CTS11572), [8] also known as NO-M214, [8] is a human Y-chromosome DNA haplogroup. NO1 is the sole confirmed subclade of Haplogroup K- M2313 (a.k.a. NO-M2313, K2a1), [9] which is the sole subclade of Haplogroup K2a (K-M2308). [6] NO is the dominant Y-DNA haplogroup in most parts of eastern and northern Eurasia, including East Asia, Siberia and northern Fennoscandia.

Contents

The location of NO1 at the SNP M214 follows the taxonomy set out by Karmin et al. 2022, [9] and conforms to a structure shown by ISOGG (2022). [8] (However neither Karmin nor ISOGG has integrated one of the findings of Poznik et al. 2016: [6] that there was a subclade generation both above haplogroup NO1 (M214) and beneath K-M2308. That is, both ISOGG and Karmin et al. continued to equate K2a with haplogroup NO.)

Before 2016, the subclades compromising both NO and NO1 were not recognised, and were regarded as synonymous with K2a. [6] Researchers such as David Poznik (Poznik et al. 2016) documented examples of previously unknown subclades of haplogroup K2, in both ancient remains and living individuals, which: (firstly) had several, varying suites of the SNPs regarded previously as uniquely defining K2a and NO, but also (secondly) lacked any of the SNPs specifically identifying haplogroups Haplogroup N (M231) and Haplogroup O (M175). [6] This demonstrated conclusively that multiple stages of development separated K2a from NO, which therefore constituted "grandparent" and "grandchild" clades. Poznik et al. 2016 used the name "K2a1" (a.k.a. K-M2313) for the Y-DNA of some of the individuals who belonged to K2a(xK2a*,NO), while also mentioning that K-M2313 did not include all examples of K2a(xK2a*,NO).

As of 2022, the International Society of Genetic Genealogy (ISOGG) refers to NO-M214 as "NO1", and to K2a (M2308)/K-M2313 as "NO". [8] There may be at least one other primary branch of NO: the ISOGG official Y-DNA haplogroup tree lists a haplogroup known as "NO1~" [ sic ] (CTS707/M2306) alongside NO-M214 (which ISOGG refers to as "NO1"). [8] The tilde (~) indicates that its exact position of NO1~ in the phylogeny is unknown. It may be a primary branch or sibling of NO, it may be a primary branch or sibling of K2a, K-M2313, or it may instead be a primary branch of K2a.

Based on the projected origins of K2a, K-M2313, and the basal haplogroups N* and O* respectively, NO* probably originated in East Asia. [5] [6]

Distribution

Migration of Haplogroup NO. Migration of the Y chromosome haplogroup N and O in East Asia.png
Migration of Haplogroup NO.

While there is some evidence of NO* being found in living individuals, these examples are not well-researched. Further research may instead identify them as belonging to N* (M231), N1, or the provisional subclade N2 (F3373/M2283/Page56/S323). [11] [12] These cases include:

Members of Haplogroup NO* include a Telugu of Indian origin sampled in the United Kingdom and a Malay sampled in Singapore. [6] [1]

Two sets of ancient remains previously considered as possibly belonging to NO have since been reclassified upstream to K2a.[ citation needed ]

Likewise, cases previously regarded as possible examples of NO* or NO1*, and since ruled out, include:

Subclades

Phylogenetic tree

This phylogeny of haplogroups K2a, K2a1, and NO is based on YFull 2018, [1] Poznik 2016, ISOGG 2018, Karafet 2008. [6] [8] [16]

K2aK-M2308 (M2308) Found only in the ancient remains "Ust'-Ishim man" (c. 45,000 BP) and "Oase 1" (c. 39,500 BP). [6]

The position of NO1~ (CTS707/M2306), a subclade of K2a1 or NO, in this phylogeny is unclear. [8]

See also

Related Research Articles

<span class="mw-page-title-main">Haplogroup</span> Group of similar haplotypes

A haplotype is a group of alleles in an organism that are inherited together from a single parent, and a haplogroup is a group of similar haplotypes that share a common ancestor with a single-nucleotide polymorphism mutation. More specifically, a haplotype is a combination of alleles at different chromosomal regions that are closely linked and that tend to be inherited together. As a haplogroup consists of similar haplotypes, it is usually possible to predict a haplogroup from haplotypes. Haplogroups pertain to a single line of descent. As such, membership of a haplogroup, by any individual, relies on a relatively small proportion of the genetic material possessed by that individual.

Haplogroup E-M96 is a human Y-chromosome DNA haplogroup. It is one of the two main branches of the older and ancestral haplogroup DE, the other main branch being haplogroup D. The E-M96 clade is divided into two main subclades: the more common E-P147, and the less common E-M75.

<span class="mw-page-title-main">Haplogroup F-M89</span> Human Y chromosome DNA grouping indicating common ancestry

Haplogroup F, also known as F-M89 and previously as Haplogroup FT, is a very common Y-chromosome haplogroup. The clade and its subclades constitute over 90% of paternal lineages outside of Africa.

Haplogroup K or K-M9 is a genetic lineage within human Y-chromosome DNA haplogroup. A sublineage of haplogroup IJK, K-M9, and its descendant clades represent a geographically widespread and diverse haplogroup. The lineages have long been found among males on every continent except Antarctica.

<span class="mw-page-title-main">Haplogroup M-P256</span> Human Y chromosome DNA grouping common in New Guinea

Haplogroup M, also known as M-P256 and Haplogroup K2b1b is a Y-chromosome DNA haplogroup. M-P256 is a descendant haplogroup of Haplogroup K2b1, and is believed to have first appeared between 32,000 and 47,000 years ago.

<span class="mw-page-title-main">Haplogroup N-M231</span> Human Y chromosome DNA grouping common in North Eurasia

Haplogroup N (M231) is a Y-chromosome DNA haplogroup defined by the presence of the single-nucleotide polymorphism (SNP) marker M231.

<span class="mw-page-title-main">Human Y-chromosome DNA haplogroup</span> Human DNA groupings

In human genetics, a human Y-chromosome DNA haplogroup is a haplogroup defined by mutations in the non-recombining portions of DNA from the male-specific Y chromosome. Many people within a haplogroup share similar numbers of short tandem repeats (STRs) and types of mutations called single-nucleotide polymorphisms (SNPs).

In human genetics, Haplogroup O-M268, also known as O1b, is a Y-chromosome DNA haplogroup. Haplogroup O-M268 is a primary subclade of haplogroup O-F265, itself a primary descendant branch of Haplogroup O-M175.

In human genetics, Haplogroup O-M119 is a Y-chromosome DNA haplogroup. Haplogroup O-M119 is a descendant branch of haplogroup O-F265 also known as O1a, one of two extant primary subclades of Haplogroup O-M175. The same clade previously has been labeled as O-MSY2.2.

Haplogroup I-M253, also known as I1, is a Y chromosome haplogroup. The genetic markers confirmed as identifying I-M253 are the SNPs M253,M307.2/P203.2, M450/S109, P30, P40, L64, L75, L80, L81, L118, L121/S62, L123, L124/S64, L125/S65, L157.1, L186, and L187. It is a primary branch of Haplogroup I-M170 (I*).

Haplogroup I-M438, also known as I2, is a human DNA Y-chromosome haplogroup, a subclade of haplogroup I-M170. Haplogroup I-M438 originated some time around 26,000–31,000 BCE. It originated in Europe and developed into several main subgroups : I2-M438*, I2a-L460, I2b-L415 and I2c-L596. The haplogroup can be found all over Europe and reaches its maximum frequency in the Dinaric Alps (Balkans) via founder effect. Examples of basal I-M438* have been found in males from Crete and Sicily.

<span class="mw-page-title-main">Haplogroup CT</span> Human Y chromosome DNA grouping indicating common ancestry

Haplogroup CT is a human Y chromosome haplogroup, defining one of the major paternal lineages of humanity.

Haplogroup K2, also known as K-M526 and formerly known as K(xLT) and MNOPS, is a human Y-DNA haplogroup.

<span class="mw-page-title-main">Haplogroup R1b</span> Type of paternal lineage

Haplogroup R1b (R-M343), previously known as Hg1 and Eu18, is a human Y-chromosome haplogroup.

In human population genetics, Y-Chromosome haplogroups define the major lineages of direct paternal (male) lines back to a shared common ancestor in Africa. Men in the same haplogroup share a set of differences, or markers, on their Y-Chromosome, which distinguish them from men in other haplogroups. These UEPs, or markers used to define haplogroups, are SNP mutations. Y-Chromosome Haplogroups all form "family trees" or "phylogenies", with both branches or sub-clades diverging from a common haplogroup ancestor, and also with all haplogroups themselves linked into one family tree which traces back ultimately to the most recent shared male line ancestor of all men alive today, called in popular science Y Chromosome Adam.

<span class="mw-page-title-main">Y-DNA haplogroups in populations of East and Southeast Asia</span>

The tables below provide statistics on the human Y-chromosome DNA haplogroups most commonly found among ethnolinguistic groups and populations from East and South-East Asia.

Haplogroup C-M48 also known as C2b1a2 is a Y-chromosome DNA haplogroup.

Haplogroup S1a is a human Y-DNA haplogroup, defined by SNPs Z41335, Z41336, Z41337, Z41338, Z41339, Z41340, and Z41341.

Haplogroup P1, also known as P-M45 and K2b2a, is a Y-chromosome DNA haplogroup in human genetics. Defined by the SNPs M45 and PF5962, P1 is a primary branch (subclade) of P.

<span class="mw-page-title-main">Haplogroup K2a (Y-DNA)</span>

Haplogroup K2a is a human Y-chromosome DNA haplogroup. K2a is a primary subclade of haplogroup K2 (M526), which in turn is a primary descendant of haplogroup K (M9). Its sole primary descendant is haplogroup K-M2313.

References

  1. 1 2 3 4 5 6 7 8 YFull YTree v5.08, 2017, "K-M2335" (9 December 2017); PhyloTree, 2017, "Details of the Y-SNP markers included in the minimal Y tree" (9 December 2017); GeneticHomeland.com, 2016, DNA Marker Index Chromosome Y V4208 (9 December 2017).
  2. 1 2 YFull Haplogroup YTree v5.06 at 25 September 2017
  3. 1 2 Karmin, Monika; Saag, Lauri; Vicente, Mário; et al. (2015). "", "A recent bottleneck of Y chromosome diversity coincides with a global change in culture". Genome Research. 25 (4): 459–466. doi:10.1101/gr.186684.114. PMC   4381518 . PMID   25770088.
  4. 1 2 G. David Poznik, Yali Xue, Fernando L. Mendez, et al., 2016, "Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences." Nature Genetics vol. 48, no. 6 (June): pp. 593–599. doi:10.1038/ng.3559.
  5. 1 2 Rootsi, Siiri; Zhivotovsky, Lev A; Baldovič, Marian; Kayser, Manfred; Kutuev, Ildus A; Khusainova, Rita; Bermisheva, Marina A; Gubina, Marina; Fedorova, Sardana A; Ilumäe, Anne-Mai; Khusnutdinova, Elza K; Voevoda, Mikhail I; Osipova, Ludmila P; Stoneking, Mark; Lin, Alice A; Ferak, Vladimir; Parik, Jüri; Kivisild, Toomas; Underhill, Peter A; Villems, Richard; et al. (2007). "A counter-clockwise northern route of the Y-chromosome haplogroup N from Southeast Asia towards Europe". European Journal of Human Genetics. 15 (2): 204–211. doi: 10.1038/sj.ejhg.5201748 . PMID   17149388.
  6. 1 2 3 4 5 6 7 8 9 10 11 12 G. David Poznik et al., 2016, "Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences" Nature Genetics, no. 48, pp. 593–599.
  7. 『DNA・考古・言語の学際研究が示す新・日本列島史 日本人集団・日本語の成立史』
  8. 1 2 3 4 5 6 7 8 9 ISOGG, Y-DNA Haplogroup Tree 2018 (17 January 2018).
  9. 1 2 Monika Karmin et al., 2022, "Episodes of Diversification and Isolation in Island Southeast Asian and Near Oceanian Male Lineages", Molecular Biology and Evolution, vol. 39, i. 3 (March). (Access: 25 January 2023.)
  10. Wang, Chuan-Chao; Li, Hui (2013-06-03). "Inferring human history in East Asia from Y chromosomes". Investigative Genetics. 4 (1): 11. doi: 10.1186/2041-2223-4-11 . ISSN   2041-2223. PMC   3687582 . PMID   23731529.
  11. 1 2 3 4 Hammer et al. (2005) "Dual origins of the Japanese: common ground for hunter-gatherer and farmer Y chromosomes," Archived 2009-03-04 at the Wayback Machine The Japan Society of Human Genetics, 2005
  12. 1 2 3 4 5 6 7 8 Xue, Yali; Zerjal, Tatiana; Bao, Weidong; Zhu, Suling; Shu, Qunfang; Xu, Jiujin; Du, Ruofu; Fu, Songbin; Li, Pu; et al. (2006). "Male demography in East Asia: a north-south contrast in human population expansion times". Genetics. 172 (4): 2431–2439. doi:10.1534/genetics.105.054270. PMC   1456369 . PMID   16489223.
  13. "Archived copy" (PDF). Archived from the original (PDF) on 2016-03-24. Retrieved 2017-03-10.{{cite web}}: CS1 maint: archived copy as title (link)
  14. Poznik, GD; Xue, Y; Mendez, FL; Willems, TF; Massaia, A; Wilson Sayres, MA; Ayub, Q; McCarthy, SA; Narechania, A; Kashin, S; Chen, Y; Banerjee, R; Rodriguez-Flores, JL; Cerezo, M; Shao, H; Gymrek, M; Malhotra, A; Louzada, S; Desalle, R; Ritchie, GR; Cerveira, E; Fitzgerald, TW; Garrison, E; Marcketta, A; Mittelman, D; Romanovitch, M; Zhang, C; Zheng-Bradley, X; Abecasis, GR; McCarroll, SA; Flicek, P; Underhill, PA; Coin, L; Zerbino, DR; Yang, F; Lee, C; Clarke, L; Auton, A; Erlich, Y; Handsaker, RE; Bustamante, CD; Tyler-Smith, C (2016). "Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences". Nat Genet. 48 (6): 593–9. doi:10.1038/ng.3559. hdl:11858/00-001M-0000-002A-F024-C. PMC   4884158 . PMID   27111036.
  15. Tatiana M. Karafet, Brian Hallmark, Murray P. Cox et al., "Major East-West Division Underlies Y Chromosome Stratification Across Indonesia," MBE Advance Access published March 5, 2010.
  16. Karafet; Mendez, F. L.; Meilerman, M. B.; Underhill, P. A.; Zegura, S. L.; Hammer, M. F.; et al. (2008). "Abstract New Binary Polymorphisms Reshape and Increase Resolution of the Human Y-Chromosomal Haplogroup Tree". Genome Research. 18 (5): 830–8. doi:10.1101/gr.7172008. PMC   2336805 . PMID   18385274.