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Haplogroup E-M215

E-M215, also known as E1b1b-M215, is a human Y-chromosome DNA haplogroup. E-M215 has two basal branches, E-M35 and E-M281. E-M35 is primarily distributed in North Africa and the Horn of Africa, and occurs at lower frequencies in the Middle East, Europe, and Southern Africa. E-M281 occurs at a low frequency in Ethiopia.

Haplogroup E-M215 (former E3b / E1b1b)
Possible time of origin47,500 - 22,400 BP[1][2][3]
Coalescence age34,800 BP[4]
Possible place of originEast Africa[5][1]
AncestorE-P2
DescendantsE-M35, E-M281
Defining mutationsM215

Origins edit

 
E1b1b1 origins map

The origins of E-M215 were dated by Cruciani in 2007 to about 22,400 years ago in East Africa.[3][Note 1]

Ancient DNA edit

According to Lazaridis et al. (2016), Natufian skeletal remains from the ancient Levant predominantly carried the Y-DNA haplogroup E1b1b. Of the five Natufian specimens analysed for paternal lineages, three belonged to the E1b1b1b2(xE1b1b1b2a,E1b1b1b2b), E1b1(xE1b1a1,E1b1b1b1) and E1b1b1b2(xE1b1b1b2a,E1b1b1b2b) subclades (60%). Haplogroup E1b1b was also found at moderate frequencies among fossils from the ensuing Pre-Pottery Neolithic B culture, with the E1b1b1 and E1b1b1b2(xE1b1b1b2a,E1b1b1b2b) subclades observed in two of seven PPNB specimens (~29%). The scientists suggest that the Levantine early farmers may have spread southward into East Africa, bringing along Western Eurasian and Basal Eurasian ancestral components separate from that which would arrive later in North Africa.

Additionally, haplogroup E1b1b1 has been found in an ancient Egyptian mummy excavated at the Abusir el-Meleq archaeological site in Middle Egypt, which dates from a period between the late New Kingdom and the Roman era.[6] Fossils at the Iberomaurusian site of Ifri N'Amr Ou Moussa in Morocco, which have been dated to around 5,000 BCE, also carried haplotypes related to the E1b1b1b1a (E-M81) subclade. These ancient individuals bore an autochthonous Maghrebi genomic component that peaks among modern North Africans, indicating that they were ancestral to populations in the area.[7] The E1b1b haplogroup has likewise been observed in ancient Guanche fossils excavated in Gran Canaria and Tenerife on the Canary Islands, which have been radiocarbon-dated to between the 7th and 11th centuries CE. The clade-bearing individuals that were analysed for paternal DNA were inhumed at the Tenerife site, with all of these specimens found to belong to the E1b1b1b1a1 or E-M183 subclade (3/3; 100%).[8]

Loosdrecht et al. (2018) analysed genome-wide data from seven ancient Iberomaurusian individuals from the Grotte des Pigeons near Taforalt in eastern Morocco. The fossils were directly dated to between 15,100 and 13,900 calibrated years before present. The scientists found that five male specimens with sufficient nuclear DNA preservation belonged to the E1b1b1a1 (M78) subclade, with one skeleton bearing the E1b1b1a1b1 parent lineage to E-V13, another male specimen belonged to E1b1b (M215*).[9]

Distribution edit

In Africa, E-M215 is distributed in highest frequencies in the Horn of Africa and North Africa, specifically in the countries Somalia and Morocco, whence it has in recent millennia expanded as far south as South Africa, and northwards into Western Asia and Europe (especially the Mediterranean and the Balkans).[10][11][12][13] E-M281 has been found in Ethiopia.[11]

Almost all E-M215 men are also in E-M35. In 2004, M215 was found to be older than M35 when individuals were found who have the M215 mutation, but do not have M35 mutation.[10] In 2013, Di Cristofaro et al. (2013) found one individual in Khorasan, North-East Iran to be positive for M215 but negative for M35.[14]

 
Geographic distribution of Y-chromosome haplogroups of select African, Middle Eastern and European populations.[15]

E-M215 and E-M35 are quite common among Afroasiatic speakers. The linguistic group and carriers of E-M35 lineage have a high probability to have arisen and dispersed together from the Afroasiatic Urheimat.[16] Amongst populations with an Afro-Asiatic speaking history, a significant proportion of Jewish male lineages are E-M35.[17] Haplogroup E-M35, which accounts for approximately 18%[11] to 20%[18][19] of Ashkenazi and 8.6%[20] to 30%[11] of Sephardi Y-chromosomes, appears to be one of the major founding lineages of the Jewish population.[21][Note 2]

E-M215 association with endurance edit

Moran et al. (2004) observed that among Y-DNA (paternal) clades borne by elite endurance athletes in Ethiopia, the haplogroup E3b1 was negatively correlated with elite athletic endurance performance,[22] whereas the haplogroups E*, E3*, K*(xP),[22] and J*(xJ2) were significantly more frequent among the elite endurance athletes.[22]

Subclades edit

E-M35 edit

Haplogroup E-M35 is a subclade of E-M215.

E-M281 edit

Haplogroup E-M281 is a subclade of E-M215.

Phylogenetics edit

Phylogenetic history edit

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
E-P29 21 III 3A 13 Eu3 H2 B E* E E E E E E E E E E
E-M33 21 III 3A 13 Eu3 H2 B E1* E1 E1a E1a E1 E1 E1a E1a E1a E1a E1a
E-M44 21 III 3A 13 Eu3 H2 B E1a E1a E1a1 E1a1 E1a E1a E1a1 E1a1 E1a1 E1a1 E1a1
E-M75 21 III 3A 13 Eu3 H2 B E2a E2 E2 E2 E2 E2 E2 E2 E2 E2 E2
E-M54 21 III 3A 13 Eu3 H2 B E2b E2b E2b E2b1 - - - - - - -
E-P2 25 III 4 14 Eu3 H2 B E3* E3 E1b E1b1 E3 E3 E1b1 E1b1 E1b1 E1b1 E1b1
E-M2 8 III 5 15 Eu2 H2 B E3a* E3a E1b1 E1b1a E3a E3a E1b1a E1b1a E1b1a E1b1a1 E1b1a1
E-M58 8 III 5 15 Eu2 H2 B E3a1 E3a1 E1b1a1 E1b1a1 E3a1 E3a1 E1b1a1 E1b1a1 E1b1a1 E1b1a1a1a E1b1a1a1a
E-M116.2 8 III 5 15 Eu2 H2 B E3a2 E3a2 E1b1a2 E1b1a2 E3a2 E3a2 E1b1a2 E1b1a2 E1ba12 removed removed
E-M149 8 III 5 15 Eu2 H2 B E3a3 E3a3 E1b1a3 E1b1a3 E3a3 E3a3 E1b1a3 E1b1a3 E1b1a3 E1b1a1a1c E1b1a1a1c
E-M154 8 III 5 15 Eu2 H2 B E3a4 E3a4 E1b1a4 E1b1a4 E3a4 E3a4 E1b1a4 E1b1a4 E1b1a4 E1b1a1a1g1c E1b1a1a1g1c
E-M155 8 III 5 15 Eu2 H2 B E3a5 E3a5 E1b1a5 E1b1a5 E3a5 E3a5 E1b1a5 E1b1a5 E1b1a5 E1b1a1a1d E1b1a1a1d
E-M10 8 III 5 15 Eu2 H2 B E3a6 E3a6 E1b1a6 E1b1a6 E3a6 E3a6 E1b1a6 E1b1a6 E1b1a6 E1b1a1a1e E1b1a1a1e
E-M35 25 III 4 14 Eu4 H2 B E3b* E3b E1b1b1 E1b1b1 E3b1 E3b1 E1b1b1 E1b1b1 E1b1b1 removed removed
E-M78 25 III 4 14 Eu4 H2 B E3b1* E3b1 E1b1b1a E1b1b1a1 E3b1a E3b1a E1b1b1a E1b1b1a E1b1b1a E1b1b1a1 E1b1b1a1
E-M148 25 III 4 14 Eu4 H2 B E3b1a E3b1a E1b1b1a3a E1b1b1a1c1 E3b1a3a E3b1a3a E1b1b1a3a E1b1b1a3a E1b1b1a3a E1b1b1a1c1 E1b1b1a1c1
E-M81 25 III 4 14 Eu4 H2 B E3b2* E3b2 E1b1b1b E1b1b1b1 E3b1b E3b1b E1b1b1b E1b1b1b E1b1b1b E1b1b1b1 E1b1b1b1a
E-M107 25 III 4 14 Eu4 H2 B E3b2a E3b2a E1b1b1b1 E1b1b1b1a E3b1b1 E3b1b1 E1b1b1b1 E1b1b1b1 E1b1b1b1 E1b1b1b1a E1b1b1b1a1
E-M165 25 III 4 14 Eu4 H2 B E3b2b E3b2b E1b1b1b2 E1b1b1b1b1 E3b1b2 E3b1b2 E1b1b1b2a E1b1b1b2a E1b1b1b2a E1b1b1b2a E1b1b1b1a2a
E-M123 25 III 4 14 Eu4 H2 B E3b3* E3b3 E1b1b1c E1b1b1c E3b1c E3b1c E1b1b1c E1b1b1c E1b1b1c E1b1b1c E1b1b1b2a
E-M34 25 III 4 14 Eu4 H2 B E3b3a* E3b3a E1b1b1c1 E1b1b1c1 E3b1c1 E3b1c1 E1b1b1c1 E1b1b1c1 E1b1b1c1 E1b1b1c1 E1b1b1b2a1
E-M136 25 III 4 14 Eu4 H2 B E3ba1 E3b3a1 E1b1b1c1a E1b1b1c1a1 E3b1c1a E3b1c1a E1b1b1c1a1 E1b1b1c1a1 E1b1b1c1a1 E1b1b1c1a1 E1b1b1b2a1a1

Research publications edit

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

Discussion edit

E-M215 and E1b1b1 are the currently accepted names found in the proposals of the Y Chromosome Consortium (YCC), for the clades defined by mutation M215 and M35 respectively, which can also be referred to as E-M215 and E-M35.[23] The nomenclature E3b (E-M215) and E3b1 (E-M35) respectively were the YCC defined names used to designate the same haplogroups in older literature with E-M35 branching as a separate subclade of E-M215 in 2004.[10] Prior to 2002 these haplogroups were not designated in a consistent way, and nor was their relationship to other related clades within haplogroup E and haplogroup DE. But in non-standard or older terminologies, E-M215 is for example approximately the same as "haplotype V", still used in publications such as Gérard et al. (2006).[24]

Phylogenetic trees edit

Cladogram with the main subclades:

E1b1b (M215

The following phylogenetic tree is based on the YCC 2008 tree and subsequent published research as summarized by ISOGG. It includes all known subclades as of June 2015 (Trombetta et al. 2015)[25][23][24]

  • E-M215 (E1b1b)
    • E-M215*. Rare or non-existent.
    • E-M35 (E1b1b1)
      • E-V68 (E1b1b1a)
        • E-V2009. Found in individuals in Sardinia and Morocco.
        • E-M78 (E1b1b1a1). North Africa, Horn of Africa, West Asia, Sicily. (Formerly "E1b1b1a".)
          • E-M78*
          • E-V1477. Found in Tunisian Jews.
          • E-V1083.
            • E-V1083*. Found only in Eritrea (1.1%) and Sardinia (0.3%).
            • E-V13
            • E-V22
          • E-V1129
            • E-V12
              • E-V12*
              • E-V32
            • E-V264
              • E-V259. Found in North Cameroon.
              • E-V65
                • E-CTS194
      • E-Z827 (E1b1b1b)[26]
        • E-V257/L19 (L19, V257) – E1b1b1b1[26]
          • E-PF2431
          • E-M81 (M81)
            • E-PF2546
              • E-PF2546*
              • E-CTS12227
                • E-MZ11
                  • E-MZ12
              • E-A929
                • E-Z5009
                  • E-Z5009*
                  • E-Z5010
                  • E-Z5013
                    • E-Z5013*
                    • E-A1152
                • E-A2227
                  • E-A428
                  • E-MZ16
                • E-PF6794
                  • E-PF6794*
                  • E-PF6789
                    • E-MZ21
                    • E-MZ23
                    • E-MZ80
                • E-A930
                • E-Z2198/E-MZ46
                  • E-A601
                  • E-L351
        • E-Z830 (Z830) – E1b1b1b2[26]
          • E-M123 (M123)
            • E-M34 (M34)
              • E-M84 (M84)
                • E-M136 (M136)
              • E-M290 (M290)
              • E-V23 (V23)
              • E-L791 (L791,L792)
          • E-V1515. E-V1515 and its subclades are mainly restricted to eastern Africa.
            • E-V1515*
            • E-V1486
              • E-V1486*
              • E-V2881
                • E-V2881*
                • E-V1792
                • E-V92
              • E-M293 (M293)
                • E-M293*
                • E-P72 (P72)
                • E-V3065*
            • E-V1700
              • E-V42 (V42)
              • E-V1785
                • E-V1785*
                • E-V6 (V6)
      • E-V16/E-M281 (E1b1b2). Rare. Found in individuals in Ethiopia, Yemen and Saudi Arabia.

See also edit

Genetics edit

Y-DNA E subclades edit

Y-DNA backbone tree edit

Notes edit

  1. ^ Cruciani et al. (2004): "Several observations point to eastern Africa as the homeland for haplogroup E3b—that is, it had (1) the highest number of different E3b clades (table 1), (2) a high frequency of this haplogroup and a high microsatellite diversity, and, finally, (3) the exclusive presence of the undifferentiated E3b* paragroup." As mentioned above, "E3b" is the old name for E-M215. Semino et al. (2004): "This inference is further supported by the presence of additional Hg E lineal diversification and by the highest frequency of E-P2* and E-M35* in the same region. The distribution of E-P2* appears limited to eastern African peoples. The E-M35* lineage shows its highest frequency (19.2%) in the Ethiopian Oromo but with a wider distribution range than E-P2*." For E-M215 Cruciani et al. (2007) reduced their estimate to 22,400 from 25,600 in Cruciani et al. (2004), re-calibrating the same data.
  2. ^ "Paragroup E-M35 * and haplogroup J-12f2a* fit the criteria for major AJ founding lineages because they are widespread both in AJ populations and in Near Eastern populations, and occur at much lower frequencies in European non-Jewish populations." Behar et al. (2004)

References edit

  1. ^ a b Trombetta 2015.
  2. ^ Haber M, Jones AL, Connel BA, Asan, Arciero E, Huanming Y, Thomas MG, Xue Y, Tyler-Smith C (June 2019). "A Rare Deep-Rooting D0 African Y-chromosomal Haplogroup and its Implications for the Expansion of Modern Humans Out of Africa". Genetics. 212 (4): 1421–1428. doi:10.1534/genetics.119.302368. PMC 6707464. PMID 31196864.
  3. ^ a b Cruciani et al. (2007)
  4. ^ "E-M215 YTree".
  5. ^ Cruciani et al. (2004).
  6. ^ Schuenemann, Verena J.; et al. (2017). "Ancient Egyptian mummy genomes suggest an increase of Sub-Saharan African ancestry in post-Roman periods". Nature Communications. 8: 15694. Bibcode:2017NatCo...815694S. doi:10.1038/ncomms15694. PMC 5459999. PMID 28556824.
  7. ^ Fregel; et al. (2018). "Ancient genomes from North Africa evidence prehistoric migrations to the Maghreb from both the Levant and Europe". bioRxiv 10.1101/191569.
  8. ^ Rodrı́guez-Varela; et al. (2017). "Genomic Analyses of Pre-European Conquest Human Remains from the Canary Islands Reveal Close Affinity to Modern North Africans". Current Biology. 27 (1–7): 3396–3402.e5. doi:10.1016/j.cub.2017.09.059. hdl:2164/13526. PMID 29107554.
  9. ^ Van De Loosdrecht, Marieke; Bouzouggar, Abdeljalil; Humphrey, Louise; Posth, Cosimo; Barton, Nick; Aximu-Petri, Ayinuer; Nickel, Birgit; Nagel, Sarah; Talbi, El Hassan; El Hajraoui, Mohammed Abdeljalil; Amzazi, Saaïd; Hublin, Jean-Jacques; Pääbo, Svante; Schiffels, Stephan; Meyer, Matthias; Haak, Wolfgang; Jeong, Choongwon; Krause, Johannes (4 May 2018). "Pleistocene North African genomes link Near Eastern and sub-Saharan African human populations". Science. 360 (6388): 548–552. Bibcode:2018Sci...360..548V. doi:10.1126/science.aar8380. PMID 29545507. S2CID 206666517.
  10. ^ a b c Cruciani et al. (2004)
  11. ^ a b c d Semino et al. (2004)
  12. ^ Rosser et al. (2000)
  13. ^ Firasat et al. (2006)
  14. ^ Di Cristofaro, Julie; et al. (October 18, 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. ISSN 1932-6203. OCLC 5534533323. PMC 3799995. PMID 24204668. S2CID 16455960.
  15. ^ Badro, Danielle A.; Douaihy, Bouchra; Haber, Marc; Youhanna, Sonia C.; Salloum, Angélique; Ghassibe-Sabbagh, Michella; Johnsrud, Brian; Khazen, Georges; Matisoo-Smith, Elizabeth; Soria-Hernanz, David F.; Wells, R. Spencer; Tyler-Smith, Chris; Platt, Daniel E.; Zalloua, Pierre A.; Consortium, The Genographic (2013-01-30). "Y-Chromosome and mtDNA Genetics Reveal Significant Contrasts in Affinities of Modern Middle Eastern Populations with European and African Populations". PLOS ONE. 8 (1): e54616. Bibcode:2013PLoSO...854616B. doi:10.1371/journal.pone.0054616. ISSN 1932-6203. PMC 3559847. PMID 23382925.
  16. ^ Ehret, Keita & Newman (2004); Keita & Boyce (2005); Keita (2008).
  17. ^ Behar et al. (2003)
  18. ^ Behar et al. (2004)
  19. ^ Shen et al. (2004)
  20. ^ Adams et al. (2008)
  21. ^ Nebel et al. (2001)
  22. ^ a b c Moran, Colin N.; et al. (2004). "Y chromosome haplogroups of elite Ethiopian endurance runners". Human Genetics. 115 (6): 492–7. doi:10.1007/s00439-004-1202-y. PMID 15503146. S2CID 13960753. Retrieved 6 February 2017.
  23. ^ a b Karafet et al. (2008)
  24. ^ a b Y Chromosome Consortium "YCC" (2002)
  25. ^ ISOGG (2011)
  26. ^ a b c ISOGG 2015

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Sources for conversion tables edit

  • Capelli, Cristian; Wilson, James F.; Richards, Martin; Stumpf, Michael P.H.; et al. (February 2001). "A Predominantly Indigenous Paternal Heritage for the Austronesian-Speaking Peoples of Insular Southeast Asia and Oceania". The American Journal of Human Genetics. 68 (2): 432–443. doi:10.1086/318205. PMC 1235276. PMID 11170891.
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  • Karafet, Tatiana; Xu, Liping; Du, Ruofu; Wang, William; et al. (September 2001). "Paternal Population History of East Asia: Sources, Patterns, and Microevolutionary Processes". The American Journal of Human Genetics. 69 (3): 615–628. doi:10.1086/323299. PMC 1235490. PMID 11481588.
  • Semino, O.; Passarino, G; Oefner, PJ; Lin, AA; et al. (2000), "The Genetic Legacy of Paleolithic Homo sapiens sapiens in Extant Europeans: A Y Chromosome Perspective", Science, 290 (5494): 1155–9, Bibcode:2000Sci...290.1155S, doi:10.1126/science.290.5494.1155, PMID 11073453
  • Su, Bing; Xiao, Junhua; Underhill, Peter; Deka, Ranjan; et al. (December 1999). "Y-Chromosome Evidence for a Northward Migration of Modern Humans into Eastern Asia during the Last Ice Age". The American Journal of Human Genetics. 65 (6): 1718–1724. doi:10.1086/302680. PMC 1288383. PMID 10577926.
  • Underhill, Peter A.; Shen, Peidong; Lin, Alice A.; Jin, Li; et al. (November 2000). "Y chromosome sequence variation and the history of human populations". Nature Genetics. 26 (3): 358–361. doi:10.1038/81685. PMID 11062480. S2CID 12893406.

haplogroup, m215, redirects, here, pennsylvania, railroad, locomotive, m215, also, known, e1b1b, m215, human, chromosome, haplogroup, m215, basal, branches, m281, primarily, distributed, north, africa, horn, africa, occurs, lower, frequencies, middle, east, eu. E3b redirects here For the Pennsylvania Railroad locomotive see PRR E3b E M215 also known as E1b1b M215 is a human Y chromosome DNA haplogroup E M215 has two basal branches E M35 and E M281 E M35 is primarily distributed in North Africa and the Horn of Africa and occurs at lower frequencies in the Middle East Europe and Southern Africa E M281 occurs at a low frequency in Ethiopia Haplogroup E M215 former E3b E1b1b Possible time of origin47 500 22 400 BP 1 2 3 Coalescence age34 800 BP 4 Possible place of originEast Africa 5 1 AncestorE P2DescendantsE M35 E M281Defining mutationsM215 Contents 1 Origins 2 Ancient DNA 3 Distribution 3 1 E M215 association with endurance 4 Subclades 4 1 E M35 4 2 E M281 5 Phylogenetics 5 1 Phylogenetic history 5 1 1 Research publications 5 1 2 Discussion 5 1 3 Phylogenetic trees 6 See also 6 1 Genetics 6 2 Y DNA E subclades 6 3 Y DNA backbone tree 7 Notes 8 References 9 Bibliography 9 1 Sources for conversion tablesOrigins edit nbsp E1b1b1 origins mapThe origins of E M215 were dated by Cruciani in 2007 to about 22 400 years ago in East Africa 3 Note 1 Ancient DNA editAccording to Lazaridis et al 2016 Natufian skeletal remains from the ancient Levant predominantly carried the Y DNA haplogroup E1b1b Of the five Natufian specimens analysed for paternal lineages three belonged to the E1b1b1b2 xE1b1b1b2a E1b1b1b2b E1b1 xE1b1a1 E1b1b1b1 and E1b1b1b2 xE1b1b1b2a E1b1b1b2b subclades 60 Haplogroup E1b1b was also found at moderate frequencies among fossils from the ensuing Pre Pottery Neolithic B culture with the E1b1b1 and E1b1b1b2 xE1b1b1b2a E1b1b1b2b subclades observed in two of seven PPNB specimens 29 The scientists suggest that the Levantine early farmers may have spread southward into East Africa bringing along Western Eurasian and Basal Eurasian ancestral components separate from that which would arrive later in North Africa Additionally haplogroup E1b1b1 has been found in an ancient Egyptian mummy excavated at the Abusir el Meleq archaeological site in Middle Egypt which dates from a period between the late New Kingdom and the Roman era 6 Fossils at the Iberomaurusian site of Ifri N Amr Ou Moussa in Morocco which have been dated to around 5 000 BCE also carried haplotypes related to the E1b1b1b1a E M81 subclade These ancient individuals bore an autochthonous Maghrebi genomic component that peaks among modern North Africans indicating that they were ancestral to populations in the area 7 The E1b1b haplogroup has likewise been observed in ancient Guanche fossils excavated in Gran Canaria and Tenerife on the Canary Islands which have been radiocarbon dated to between the 7th and 11th centuries CE The clade bearing individuals that were analysed for paternal DNA were inhumed at the Tenerife site with all of these specimens found to belong to the E1b1b1b1a1 or E M183 subclade 3 3 100 8 Loosdrecht et al 2018 analysed genome wide data from seven ancient Iberomaurusian individuals from the Grotte des Pigeons near Taforalt in eastern Morocco The fossils were directly dated to between 15 100 and 13 900 calibrated years before present The scientists found that five male specimens with sufficient nuclear DNA preservation belonged to the E1b1b1a1 M78 subclade with one skeleton bearing the E1b1b1a1b1 parent lineage to E V13 another male specimen belonged to E1b1b M215 9 Distribution editIn Africa E M215 is distributed in highest frequencies in the Horn of Africa and North Africa specifically in the countries Somalia and Morocco whence it has in recent millennia expanded as far south as South Africa and northwards into Western Asia and Europe especially the Mediterranean and the Balkans 10 11 12 13 E M281 has been found in Ethiopia 11 Almost all E M215 men are also in E M35 In 2004 M215 was found to be older than M35 when individuals were found who have the M215 mutation but do not have M35 mutation 10 In 2013 Di Cristofaro et al 2013 found one individual in Khorasan North East Iran to be positive for M215 but negative for M35 14 nbsp Geographic distribution of Y chromosome haplogroups of select African Middle Eastern and European populations 15 E M215 and E M35 are quite common among Afroasiatic speakers The linguistic group and carriers of E M35 lineage have a high probability to have arisen and dispersed together from the Afroasiatic Urheimat 16 Amongst populations with an Afro Asiatic speaking history a significant proportion of Jewish male lineages are E M35 17 Haplogroup E M35 which accounts for approximately 18 11 to 20 18 19 of Ashkenazi and 8 6 20 to 30 11 of Sephardi Y chromosomes appears to be one of the major founding lineages of the Jewish population 21 Note 2 E M215 association with endurance edit Moran et al 2004 observed that among Y DNA paternal clades borne by elite endurance athletes in Ethiopia the haplogroup E3b1 was negatively correlated with elite athletic endurance performance 22 whereas the haplogroups E E3 K xP 22 and J xJ2 were significantly more frequent among the elite endurance athletes 22 Subclades editE M35 edit Main article Haplogroup E M35 Haplogroup E M35 is a subclade of E M215 E M281 edit Main article Haplogroup E M281 Haplogroup E M281 is a subclade of E M215 Phylogenetics editPhylogenetic 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 a b g d e z h 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 2012E P29 21 III 3A 13 Eu3 H2 B E E E E E E E E E E EE M33 21 III 3A 13 Eu3 H2 B E1 E1 E1a E1a E1 E1 E1a E1a E1a E1a E1aE M44 21 III 3A 13 Eu3 H2 B E1a E1a E1a1 E1a1 E1a E1a E1a1 E1a1 E1a1 E1a1 E1a1E M75 21 III 3A 13 Eu3 H2 B E2a E2 E2 E2 E2 E2 E2 E2 E2 E2 E2E M54 21 III 3A 13 Eu3 H2 B E2b E2b E2b E2b1 E P2 25 III 4 14 Eu3 H2 B E3 E3 E1b E1b1 E3 E3 E1b1 E1b1 E1b1 E1b1 E1b1E M2 8 III 5 15 Eu2 H2 B E3a E3a E1b1 E1b1a E3a E3a E1b1a E1b1a E1b1a E1b1a1 E1b1a1E M58 8 III 5 15 Eu2 H2 B E3a1 E3a1 E1b1a1 E1b1a1 E3a1 E3a1 E1b1a1 E1b1a1 E1b1a1 E1b1a1a1a E1b1a1a1aE M116 2 8 III 5 15 Eu2 H2 B E3a2 E3a2 E1b1a2 E1b1a2 E3a2 E3a2 E1b1a2 E1b1a2 E1ba12 removed removedE M149 8 III 5 15 Eu2 H2 B E3a3 E3a3 E1b1a3 E1b1a3 E3a3 E3a3 E1b1a3 E1b1a3 E1b1a3 E1b1a1a1c E1b1a1a1cE M154 8 III 5 15 Eu2 H2 B E3a4 E3a4 E1b1a4 E1b1a4 E3a4 E3a4 E1b1a4 E1b1a4 E1b1a4 E1b1a1a1g1c E1b1a1a1g1cE M155 8 III 5 15 Eu2 H2 B E3a5 E3a5 E1b1a5 E1b1a5 E3a5 E3a5 E1b1a5 E1b1a5 E1b1a5 E1b1a1a1d E1b1a1a1dE M10 8 III 5 15 Eu2 H2 B E3a6 E3a6 E1b1a6 E1b1a6 E3a6 E3a6 E1b1a6 E1b1a6 E1b1a6 E1b1a1a1e E1b1a1a1eE M35 25 III 4 14 Eu4 H2 B E3b E3b E1b1b1 E1b1b1 E3b1 E3b1 E1b1b1 E1b1b1 E1b1b1 removed removedE M78 25 III 4 14 Eu4 H2 B E3b1 E3b1 E1b1b1a E1b1b1a1 E3b1a E3b1a E1b1b1a E1b1b1a E1b1b1a E1b1b1a1 E1b1b1a1E M148 25 III 4 14 Eu4 H2 B E3b1a E3b1a E1b1b1a3a E1b1b1a1c1 E3b1a3a E3b1a3a E1b1b1a3a E1b1b1a3a E1b1b1a3a E1b1b1a1c1 E1b1b1a1c1E M81 25 III 4 14 Eu4 H2 B E3b2 E3b2 E1b1b1b E1b1b1b1 E3b1b E3b1b E1b1b1b E1b1b1b E1b1b1b E1b1b1b1 E1b1b1b1aE M107 25 III 4 14 Eu4 H2 B E3b2a E3b2a E1b1b1b1 E1b1b1b1a E3b1b1 E3b1b1 E1b1b1b1 E1b1b1b1 E1b1b1b1 E1b1b1b1a E1b1b1b1a1E M165 25 III 4 14 Eu4 H2 B E3b2b E3b2b E1b1b1b2 E1b1b1b1b1 E3b1b2 E3b1b2 E1b1b1b2a E1b1b1b2a E1b1b1b2a E1b1b1b2a E1b1b1b1a2aE M123 25 III 4 14 Eu4 H2 B E3b3 E3b3 E1b1b1c E1b1b1c E3b1c E3b1c E1b1b1c E1b1b1c E1b1b1c E1b1b1c E1b1b1b2aE M34 25 III 4 14 Eu4 H2 B E3b3a E3b3a E1b1b1c1 E1b1b1c1 E3b1c1 E3b1c1 E1b1b1c1 E1b1b1c1 E1b1b1c1 E1b1b1c1 E1b1b1b2a1E M136 25 III 4 14 Eu4 H2 B E3ba1 E3b3a1 E1b1b1c1a E1b1b1c1a1 E3b1c1a E3b1c1a E1b1b1c1a1 E1b1b1c1a1 E1b1b1c1a1 E1b1b1c1a1 E1b1b1b2a1a1Research publications edit The following research teams per their publications were represented in the creation of the YCC Tree a Jobling amp Tyler Smith 2000 and Kaladjieva 2001 b Underhill 2000 g Hammer 2001 d Karafet 2001 e Semino 2000 z Su 1999 h Capelli 2001 Discussion edit E M215 and E1b1b1 are the currently accepted names found in the proposals of the Y Chromosome Consortium YCC for the clades defined by mutation M215 and M35 respectively which can also be referred to as E M215 and E M35 23 The nomenclature E3b E M215 and E3b1 E M35 respectively were the YCC defined names used to designate the same haplogroups in older literature with E M35 branching as a separate subclade of E M215 in 2004 10 Prior to 2002 these haplogroups were not designated in a consistent way and nor was their relationship to other related clades within haplogroup E and haplogroup DE But in non standard or older terminologies E M215 is for example approximately the same as haplotype V still used in publications such as Gerard et al 2006 24 Phylogenetic trees edit Cladogram with the main subclades E1b1b M215 E1b1b1 M35 E1b1b1a V68 E M78 E V12E V65E V13E V22E V2729E1b1b1b Z827 E M81E M123E1b1b2 M281 The following phylogenetic tree is based on the YCC 2008 tree and subsequent published research as summarized by ISOGG It includes all known subclades as of June 2015 Trombetta et al 2015 25 23 24 E M215 E1b1b E M215 Rare or non existent E M35 E1b1b1 E V68 E1b1b1a E V2009 Found in individuals in Sardinia and Morocco E M78 E1b1b1a1 North Africa Horn of Africa West Asia Sicily Formerly E1b1b1a E M78 E V1477 Found in Tunisian Jews E V1083 E V1083 Found only in Eritrea 1 1 and Sardinia 0 3 E V13 E V22 E V1129 E V12 E V12 E V32 E V264 E V259 Found in North Cameroon E V65 E CTS194 E Z827 E1b1b1b 26 E V257 L19 L19 V257 E1b1b1b1 26 E PF2431 E M81 M81 E PF2546 E PF2546 E CTS12227 E MZ11 E MZ12 E A929 E Z5009 E Z5009 E Z5010 E Z5013 E Z5013 E A1152 E A2227 E A428 E MZ16 E PF6794 E PF6794 E PF6789 E MZ21 E MZ23 E MZ80 E A930 E Z2198 E MZ46 E A601 E L351 E Z830 Z830 E1b1b1b2 26 E M123 M123 E M34 M34 E M84 M84 E M136 M136 E M290 M290 E V23 V23 E L791 L791 L792 E V1515 E V1515 and its subclades are mainly restricted to eastern Africa E V1515 E V1486 E V1486 E V2881 E V2881 E V1792 E V92 E M293 M293 E M293 E P72 P72 E V3065 E V1700 E V42 V42 E V1785 E V1785 E V6 V6 E V16 E M281 E1b1b2 Rare Found in individuals in Ethiopia Yemen and Saudi Arabia See also edit nbsp Wikiquote has quotations related to Haplogroup E M215 Genetics edit African admixture in Europe genetic genealogy Haplogroup D Haplogroup DE Haplogroup Haplotype Human Y chromosome DNA haplogroup Molecular phylogenetics Paragroup Subclade Y chromosome haplogroups in populations of the world Y DNA haplogroups by ethnic group Y DNA haplogroups in populations of Sub Saharan Africa Y DNA E subclades edit Haplogroup E L485 Haplogroup E M123 Haplogroup E M180 Haplogroup E M215 Haplogroup E M33 Haplogroup E M521 Haplogroup E M75 Haplogroup E M96 Haplogroup E P147 Haplogroup E P177 Haplogroup E P2 Haplogroup E V12 Haplogroup E V13 Haplogroup E V22 Haplogroup E M2 Haplogroup E V65 Haplogroup E V68 Haplogroup E Z820 Haplogroup E Z827 Y DNA backbone tree editNotes edit Cruciani et al 2004 Several observations point to eastern Africa as the homeland for haplogroup E3b that is it had 1 the highest number of different E3b clades table 1 2 a high frequency of this haplogroup and a high microsatellite diversity and finally 3 the exclusive presence of the undifferentiated E3b paragroup As mentioned above E3b is the old name for E M215 Semino et al 2004 This inference is further supported by the presence of additional Hg E lineal diversification and by the highest frequency of E P2 and E M35 in the same region The distribution of E P2 appears limited to eastern African peoples The E M35 lineage shows its highest frequency 19 2 in the Ethiopian Oromo but with a wider distribution range than E P2 For E M215 Cruciani et al 2007 reduced their estimate to 22 400 from 25 600 in Cruciani et al 2004 re calibrating the same data Paragroup E M35 and haplogroup J 12f2a fit the criteria for major AJ founding lineages because they are widespread both in AJ populations and in Near Eastern populations and occur at much lower frequencies in European non Jewish populations Behar et al 2004 References edit a b Trombetta 2015 Haber M Jones AL Connel BA Asan Arciero E Huanming Y Thomas MG Xue Y Tyler Smith C June 2019 A Rare Deep Rooting D0 African Y chromosomal Haplogroup and its Implications for the Expansion of Modern Humans Out of Africa Genetics 212 4 1421 1428 doi 10 1534 genetics 119 302368 PMC 6707464 PMID 31196864 a b Cruciani et al 2007 E M215 YTree Cruciani et al 2004 Schuenemann Verena J et al 2017 Ancient Egyptian mummy genomes suggest an increase of Sub Saharan African ancestry in post Roman periods Nature Communications 8 15694 Bibcode 2017NatCo 815694S doi 10 1038 ncomms15694 PMC 5459999 PMID 28556824 Fregel et al 2018 Ancient genomes from North Africa evidence prehistoric migrations to the Maghreb from both the Levant and Europe bioRxiv 10 1101 191569 Rodri guez Varela et al 2017 Genomic Analyses of Pre European Conquest Human Remains from the Canary Islands Reveal Close Affinity to Modern North Africans Current Biology 27 1 7 3396 3402 e5 doi 10 1016 j cub 2017 09 059 hdl 2164 13526 PMID 29107554 Van De Loosdrecht Marieke Bouzouggar Abdeljalil Humphrey Louise Posth Cosimo Barton Nick Aximu Petri Ayinuer Nickel Birgit Nagel Sarah Talbi El Hassan El Hajraoui Mohammed Abdeljalil Amzazi Saaid Hublin Jean Jacques Paabo Svante Schiffels Stephan Meyer Matthias Haak Wolfgang Jeong Choongwon Krause Johannes 4 May 2018 Pleistocene North African genomes link Near Eastern and sub Saharan African human populations Science 360 6388 548 552 Bibcode 2018Sci 360 548V doi 10 1126 science aar8380 PMID 29545507 S2CID 206666517 a b c Cruciani et al 2004 a b c d Semino et al 2004 Rosser et al 2000 Firasat et al 2006 Di Cristofaro Julie et al October 18 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 ISSN 1932 6203 OCLC 5534533323 PMC 3799995 PMID 24204668 S2CID 16455960 Badro Danielle A Douaihy Bouchra Haber Marc Youhanna Sonia C Salloum Angelique Ghassibe Sabbagh Michella Johnsrud Brian Khazen Georges Matisoo Smith Elizabeth Soria Hernanz David F Wells R Spencer Tyler Smith Chris Platt Daniel E Zalloua Pierre A Consortium The Genographic 2013 01 30 Y Chromosome and mtDNA Genetics Reveal Significant Contrasts in Affinities of Modern Middle Eastern Populations with European 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