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Haplogroup E-V12

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Haplogroup E-V12
Interpolated frequency distribution.[1]
Possible time of originc. 12,300 years BP[2]
Coalescence agec. 10,500 years BP[2]
Possible place of originLower Egypt/Libya[3] or Upper Egypt/Northern Sudan[4]
AncestorE-V68/M78[5]
Defining mutationsV12, Z1216[5]

The human Y-chromosome haplogroup E-V12 is a subclade of E-M78, which in turn is part of the larger haplogroup E1b1b1.[3] According to Cruciani et al. (2007), the E-V12 sublineage likely originated in Northern Africa. It has two main branches: E-V32 which is most common in the Horn of Africa, and E-CTS693 (previously known as E-V12*) which is most common in Upper Egypt and to a lesser extent in Sudan. E-CTS693 is also scattered in low frequencies across the Levant, Anatolia, the Central Sahel, the African Great Lakes region, and Europe.[6][3]

Ancient DNA

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  • One individual from Bronze Age Alalakh dated c. 1878-1637 BC belonged to haplogroup E-V12.[7] Alalakh was a city in northern Levant settled by Amorites and some Hurrians.[7]
  • One individual from imperial Rome dated c. 2000-1800 ybp (years before present) belonged to haplogroup E-V12.[8]
  • A 1st century Nubian mercenary genome from Serbia (Roman Empire) carried haplogroup E-V32 and L2a1j. On the PCA, positioning of the outlier individual supported an East African ancestral origin.[9][10]
  • One Medieval individual dated c. 1130-520 ybp from Villa Magna, Central Italy belonged to haplogroup E-V12.[8]

Undifferentiated E-V12* lineages

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Undifferentiated E-V12* lineages (not E-V32 or E-M224, so therefore named "E-V12*") peak in frequency among Southern Egyptians (up to 74.5%).[11] The subclades are also scattered widely in small amounts in both Northern Africa and Europe, but with very little sign in Western Asia, apart from Turkey.[3] These E-V12* lineages were formerly included (along with many E-V22* lineages[Note 1]) in Cruciani et al.'s original (2004) "delta cluster", which he had defined using Y-STR profiles. With the discovery of the defining SNP, Cruciani et al. (2007) reported that V12* was found in its highest concentrations in Egypt, especially Southern Egypt.

Hassan et al. (2008) report a significant presence of E-V12* in neighboring Sudan, including 5/33 Copts and 5/39 Nubians. E-V12* made up approximately 20% of the Sudanese E-M78. They propose that the E-V12 and E-V22 sub-clades of E-M78 might have been brought to Sudan from their place of origin in North Africa after the progressive desertification of the Sahara around 6,000–8,000 years ago. Sudden climate change might have forced several Neolithic cultures/people to migrate northward to the Mediterranean and southward to the Sahel and the Nile Valley.[12] The E-V12* paragroup is also observed in Europe (e.g. amongst French Basques) and Eastern Anatolia (e.g. Erzurum Turks).[3]

The non-basal subhaplogroup E1b1b-V12/E3b1a1 has been found at highest frequencies among various Afroasiatic-speaking populations in eastern Africa, including Garreh (74.1%), Gabra (58.6%), Wata (55.6%), Borana (50.0%), Sanye (41.7%), Beja (33.3%) and Rendille (29.0%).[13]

Sub-clades of E-V12

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E-V32

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Cruciani et al. (2007) suggest that this sub-clade of E-V12, which originated in North Africa, and then subsequently expanded further south into the Horn of Africa, where it is now prevalent,[Note 2] with speakers of Cushitic. Before the discovery of V32, Cruciani et al. (2004) referred to the same lineages as the "gamma cluster", which was estimated to have arisen about 8,500 years ago. They stated that "the highest frequencies in the three Cushitic-speaking groups: the Borana from Kenya (71.4%), the Oromo from Ethiopia (32.0%), and the Somali (80%). Outside of eastern Africa, it was found only in two subjects from Egypt (3.6%) and in one Arab from Morocco". Sanchez et al. (2005) found it extremely prominent in Somali men and stated that "the male Somali population is a branch of the Horn African population – closely related to the Oromos in Ethiopia and North Kenya (Boranas)" and that their gamma cluster lineages "probably were introduced into the Somali population 4000–5000 years ago". More recently, Tillmar et al. (2009) typed 147 males from Somalia for 12 Y-STR loci, and observed that 77% (113/147) had typical E-V32 haplotypes. This is currently the highest frequency of E-V32 found in any single sample population. Similarly, Hassan et al. (2008) in their study observed this to be the most common of the sub-clades of E-M78 found in Sudan, especially among the Beja, Masalit and Fur. The Beja, like Somalis and Oromos, speak an Afro-Asiatic language and live along the "corridor" from the Horn of Africa to Egypt. Hassan et al. (2008) interpret this as reinforcing the "strong correlation between linguistic and genetic diversity" and signs of relatedness between the Beja and the peoples of the Horn of Africa such as the Amhara, Oromo, and Somalis. On the other hand, the Masalit and Fur live in Darfur and speak a Nilo-Saharan language. The authors observed in their study that "the Masalit possesses by far the highest frequency of the E-M78 and of the E-V32 haplogroup", which they believe suggests "either a recent bottleneck in the population or a proximity to the origin of the haplogroup." However, More recently, Tillmar et al. (2009) typed 147 males from Somalia for 12 Y-STR loci, and observed that 77% (113/147) had typical E-V32 haplotypes. This is the highest frequency of E-V32 found in any single sample population.

The STR data from Cruciani et al. (2007) concerning E-V12 can be summarized as follows.

Haplotype description YCAIIa YCAIIb DYS413a DYS413b DYS19 DYS391 DYS393 DYS439 DYS460 DYS461 A10
E-V12* modal 19 22 22 22 13 10 13 11 11 9 13
min 18 21 20 21 11 10 12 11 8 8 11
max 19 22 22 23 15 12 14 13 12 10 14
number 40 40 40 40 40 40 40 40 40 40 40
E-V32 modal 19 21 22 23 11 10 13 12 10 10 13
min 19 19 20 21 11 9 12 11 9 10 11
max 20 22 22 24 11 11 13 13 12 11 14
number 35 35 35 35 35 35 35 35 35 35 35
All E-V12 modal 19 22 22 23 11 10 13 11 11 10 13
min 18 19 20 21 11 9 12 11 8 8 11
max 20 22 22 24 15 12 14 13 12 11 14
number 75 75 75 75 75 75 75 75 75 75 75

Sub-clades

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Notes

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  1. ^ Cruciani et al. (2004): "E-V22 and E-V12* chromosomes are intermingled and not clearly differentiated by their microsatellite haplotypes". In Cruciani et al. (2007) the same authors show that a branch of E-V13 found amongst the Druze Arabs is also in the delta cluster. (Contrast the data tables of Cruciani et al. (2007) and Cruciani et al. (2004).)
  2. ^ Cruciani et al. (2007): Fig. 2/C

References

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  1. ^ D'Atanasio E; Trombetta B; Bonito M; Finocchio A; Di Vito G; Seghizzi M; et al. (2018). "The peopling of the last Green Sahara revealed by high-coverage resequencing of trans-Saharan patrilineages". Genome Biol. 19 (1): 20. doi:10.1186/s13059-018-1393-5. PMC 5809971. PMID 29433568.
  2. ^ a b "E-V12 YTree".
  3. ^ a b c d e Cruciani et al. (2007)
  4. ^ Battaglia et al. (2008)
  5. ^ a b ISOGG, Copyright 2016 by. "ISOGG 2017 Y-DNA Haplogroup E". isogg.org. Retrieved 2019-01-07.{{cite web}}: CS1 maint: numeric names: authors list (link)
  6. ^ E-CTS693
  7. ^ a b Ingman, Tara; Eisenmann, Stefanie; Skourtanioti, Eirini; Akar, Murat; Ilgner, Jana; Gnecchi Ruscone, Guido Alberto; le Roux, Petrus; Shafiq, Rula; Neumann, Gunnar U.; Keller, Marcel; Freund, Cäcilia; Marzo, Sara; Lucas, Mary; Krause, Johannes; Roberts, Patrick; Yener, K. Aslıhan; Stockhammer, Philipp W. (2021). "Human mobility at Tell Atchana (Alalakh), Hatay, Turkey during the 2nd millennium BC: Integration of isotopic and genomic evidence". PLOS ONE. 16 (6): e0241883. Bibcode:2021PLoSO..1641883I. doi:10.1371/journal.pone.0241883. PMID 34191795.
  8. ^ a b Antonio, Margaret L.; et al. (8 November 2019). "Ancient Rome: A genetic crossroads of Europe and the Mediterranean". Science. 366 (6466). American Association for the Advancement of Science: 708–714. Bibcode:2019Sci...366..708A. doi:10.1126/science.aay6826. PMC 7093155. PMID 31699931.
  9. ^ Olalde, Iñigo; Carrión, Pablo; Mikić, Ilija; Rohland, Nadin; Mallick, Shop; Lazaridis, Iosif; Korać, Miomir; Golubović, Snežana; Petković, Sofija; Miladinović-Radmilović, Nataša; Vulović, Dragana; Stewardson, Kristin; Lawson, Ann Marie; Zalzala, Fatma; Callan, Kim (2021-08-31). "Cosmopolitanism at the Roman Danubian Frontier, Slavic Migrations, and the Genomic Formation of Modern Balkan Peoples". doi:10.1101/2021.08.30.458211. S2CID 237377452. {{cite journal}}: Cite journal requires |journal= (help)
  10. ^ Olalde, Iñigo; Carrión, Pablo; Mikić, Ilija; Rohland, Nadin; Mallick, Swapan; Lazaridis, Iosif; Mah, Matthew; Korać, Miomir; Golubović, Snežana; Petković, Sofija; Miladinović-Radmilović, Nataša; Vulović, Dragana; Alihodžić, Timka; Ash, Abigail; Baeta, Miriam (2023-12-27). "A genetic history of the Balkans from Roman frontier to Slavic migrations". Cell. 186 (25): 5472–5485.e9. doi:10.1016/j.cell.2023.10.018. ISSN 0092-8674. Archived from the original on 2024-12-16.
  11. ^ Beniamino Trombetta (2015). "Phylogeographic refinement and large scale genotyping of human Y chromosome haplogroup E provide new insights into the dispersal of early pastoralists in the African continent". Genome Biology and Evolution. 7 (7): 1940–1950. doi:10.1093/gbe/evv118. PMC 4524485. PMID 26108492.
  12. ^ Hassan et al. (2008)
  13. ^ Hirbo, Jibril Boru. "Complex Genetic History of East African Human Populations" (PDF). University of Maryland, College Park. Retrieved 13 July 2017.

Sources

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