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Haplogroup L3

Haplogroup L3 is a human mitochondrial DNA (mtDNA) haplogroup. The clade has played a pivotal role in the early dispersal of anatomically modern humans.

Haplogroup L3
Ancient dispersal of haplogroup L3, its descendant M and N lineages, and other mtDNA clades. Numbers represent thousand years before present.
Possible time of origin80,000–60,000 BP,[1] 70,000 BP[2]
Possible place of originEast Africa[3][4][5][2] or Asia[6]
AncestorL3'4
DescendantsL3a, L3b'f, L3c'd, L3e'i'k'x, L3h, M, N
Defining mutations769, 1018, 16311[7]

It is strongly associated with the out-of-Africa migration of modern humans of about 70–50,000 years ago. It is inherited by all modern non-African populations, as well as by some populations in Africa.[8][3]

Origin edit

Haplogroup L3 arose close to 70,000 years ago, near the time of the recent out-of-Africa event. This dispersal originated in East Africa and expanded to West Asia, and further to South and Southeast Asia in the course of a few millennia, and some research suggests that L3 participated in this migration out of Africa. A 2007 estimate for the age of L3 suggested a range of 104–84,000 years ago.[9] More recent analyses, including Soares et al. (2012) arrive at a more recent date, of roughly 70–60,000 years ago. Soares et al. also suggest that L3 most likely expanded from East Africa into Eurasia sometime around 65–55,000 years ago as part of the recent out-of-Africa event, as well as from East Africa into Central Africa from 60 to 35,000 years ago.[3] In 2016, Soares et al. again suggested that haplogroup L3 emerged in East Africa, leading to the Out-of-Africa migration, around 70–60,000 years ago.[10]

Haplogroups L6 and L4 form sister clades of L3 which arose in East Africa at roughly the same time but which did not participate in the out-of-Africa migration. The ancestral clade L3'4'6 has been estimated at 110 kya, and the L3'4 clade at 95 kya.[8]

 
Proposed migration route depicting the origin of L3 in Africa and its dispersal both out of and within the continent, with two possible models (as depicted by Vai et al.)[4] : (a) Haplogroup N differentiates from L3 in Africa, with a subsequent spread out of Africa, and differentiation of haplogroup M from L3 outside Africa. (b) Haplogroups M and N diverge from L3 outside Africa after the expansion of L3 from the continent; later migrations during the Upper Paleolithic and Neolithic led some lineages back to North Africa. (Haplogroups are indicated in black circles in their probable area of origin.)
 
Proposed migration route according to the Asian origin hypothesis (Cabrera et al.).[6]
a: Exit of the L3 precursor to Eurasia. b: Return to Africa and expansion to Asia of basal L3 lineages with subsequent differentiation in both continents.

The possibility of an origin of L3 in Asia was proposed by Cabrera et al. (2018) based on the similar coalescence dates of L3 and its Eurasian-distributed M and N derivative clades (ca. 70 kya), the distant location in Southeast Asia of the oldest known subclades of M and N, and the comparable age of the paternal haplogroup DE. According to this hypothesis, after an initial out-of-Africa migration of bearers of pre-L3 (L3'4*) around 125 kya, there would have been a back-migration of females carrying L3 from Eurasia to East Africa sometime after 70 kya. The hypothesis suggests that this back-migration is aligned with bearers of paternal haplogroup E, which it also proposes to have originated in Eurasia. These new Eurasian lineages are then suggested to have largely replaced the old autochthonous male and female North-East African lineages.[6]

According to other research, though earlier migrations out of Africa of anatomically modern humans occurred, current Eurasian populations descend instead from a later migration from Africa dated between about 65,000 and 50,000 years ago (associated with the migration out of L3).[11][4][12]

Vai et al. (2019) suggest, from a newly discovered old and deeply-rooted branch of maternal haplogroup N found in early Neolithic North African remains, that haplogroup L3 originated in East Africa between 70,000 and 60,000 years ago, and both spread within Africa and left Africa as part of the Out-of-Africa migration, with haplogroup N diverging from it soon after (between 65,000 and 50,000 years ago) either in Arabia or possibly North Africa, and haplogroup M originating in the Middle East around the same time as N.[4]

A study by Lipson et al. (2019) analyzing remains from the Cameroonian site of Shum Laka found them to be more similar to modern-day Pygmy peoples than to West Africans, and suggests that several other groups (including the ancestors of West Africans, East Africans and the ancestors of non-Africans) commonly derived from a human population originating in East Africa between about 80,000-60,000 years ago, which they suggest was also the source and origin zone of haplogroup L3 around 70,000 years ago.[13]

Distribution edit

 
Projected spatial distribution of haplogroup L3 in Africa and the Arabian peninsula.

L3 is common in Northeast Africa and some other parts of East Africa,[14] in contrast to others parts of Africa where the haplogroups L1 and L2 represent around two thirds of mtDNA lineages.[15] L3 sublineages are also frequent in the Arabian peninsula.

L3 is subdivided into several clades, two of which spawned the macrohaplogroups M and N that are today carried by most people outside Africa.[15] There is at least one relatively deep non-M, non-N clade of L3 outside Africa, L3f1b6, which is found at a frequency of 1% in Asturias, Spain. It diverged from African L3 lineages at least 10,000 years ago.[16]

According to Maca-Meyer et al. (2001), "L3 is more related to Eurasian haplogroups than to the most divergent African clusters L1 and L2".[17] L3 is the haplogroup from which all modern humans outside Africa derive.[18] However, there is a greater diversity of major L3 branches within Africa than outside of it, the two major non-African branches being the L3 offshoots M and N.

Subclade distribution edit

 
L3 subclade distribution: L3b, L3d, L3e, L3f, L3h, L3i, L3x and L3w.

L3 has seven equidistant descendants: L3a, L3b'f, L3c'd, L3e'i'k'x, L3h, M, N. Five are African, while two are associated with the Out of Africa event.

  • NEurasia possibly due to migration from Africa, and North Africa possibly due to back-migration from Eurasia.[3][6][4]
  • MAsia, the Mediterranean Basin, and parts of Africa due to back-migration.[3][6]
  • L3a – East Africa.[8][3] Moderate to high frequencies found among the Sanye, Samburu, Iraqw, Yaaku, El-Molo and other minor indigenous populations from the East African Rift Valley. It is infrequent to nonexistent in Sudan and the Sahel zone.[19]
    • L3a1 – Found across Eastern Africa. Estimated age of 35.8–39.3 ka.[3]
    • L3a2 – Found across Eastern Africa. Estimated age of 48.3–57.7 ka.[20]
  • L3b'f
    • L3b – Spread from East Africa in the upper paleolithic to West-Central Africa. Some subclades spread from Central Africa to East Africa with the Bantu migration.[3]
      • L3b1a – Common subclade. Estimated age of 11.7-14.8 ka.[3]
        • L3b1a2 – Subclade found in Northeast Africa, the Maghreb, and Middle East. Emerged 12–14 ka.[21][20]
    • L3f – Northeast Africa, Sahel, Arabian peninsula, Iberia. Gaalien,[22] Beja[22]
      • L3f1
        • L3f1a – Carried by migrants from Eastern Africa into the Sahel and Central Africa.[3]
        • L3f1b – Carried by migrants from Eastern Africa into the Sahel and Central Africa.[3]
          • L3f1b1 – Carried from Central Africa into Southern and Eastern Africa with the Bantu migration.[3]
            • L3f1b1a – Settled from East-Central Africa to Central-West Africa and into North Africa and Berber regions.[3]
          • L3f1b4 – Carried from Central Africa into Southern and Eastern Africa with the Bantu migration.[3]
        • L3f1b6 – Rare, found in Iberia.[16]
      • L3f2 – Primarily distributed in East Africa.[3] Also found in North Africa and Central Africa.[21]
      • L3f3 – Spread from Eastern Africa to Chad and the Sahel around 8–9 ka.[3] Found in the Chad Basin.[21][23]
  • L3c'd
  • L3e'i'k'x
  • L3h – Almost exclusively found in East Africa.[3]
    • L3h1 – Primarily found in East Africa with branches of L3h1b1 sporadically found in the Sahel and North Africa.[20][21]
    • L3h2 – Found in Northeast Africa and Socotra. Split from other L3h branches as early as 65–69 ka during the middle paleolithic.[20][21]

Ancient and historic samples edit

Haplogroup L3 has been observed in an ancient fossil belonging to the Pre-Pottery Neolithic B culture.[35] L3x2a was observed in a 4,500 year old hunter-gather excavated in Mota, Ethiopia, with the ancient fossil found to be most closely related to modern Southwest Ethiopian populations.[36][37] Haplogroup L3 has also been found among ancient Egyptian mummies (1/90; 1%) excavated at the Abusir el-Meleq archaeological site in Middle Egypt, with the rest deriving from Eurasian subclades, which date from the Pre-Ptolemaic/late New Kingdom and Ptolemaic periods. The Ancient Egyptian mummies bore Near eastern genomic component most closely related to modern near easterners.[38] Additionally, haplogroup L3 has 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. All of the clade-bearing individuals were inhumed at the Gran Canaria site, with most of these specimens found to belong to the L3b1a subclade (3/4; 75%) with the rest from both islands (8/11; 72%) deriving from Eurasian subclades. The Guanche skeletons also bore an autochthonous Maghrebi genomic component that peaks among modern Berbers, which suggests that they originated from ancestral Berber populations inhabiting northwestern Affoundnat a high ncy[39]

A variety of L3 have been uncovered in ancient remains associated with the Pastoral Neolithic and Pastoral Iron Age of East Africa.[40]

Culture Genetic cluster or affinity Country Site Date Maternal Haplogroup Paternal Haplogroup Source
Early pastoral PN Kenya Prettejohn's Gully (GsJi11) 4060–3860 L3f1b Prendergast 2019
Pastoral Neolithic PN Kenya Cole's Burial (GrJj5a) 3350–3180 L3i2 E-V32 Prendergast 2019
Pastoral Neolithic or Elmenteitan PN Kenya Rigo Cave (GrJh3) 2710–2380 L3f E-M293 Prendergast 2019
Pastoral Neolithic PN Kenya Naishi Rockshelter 2750–2500 L3x1a E-V1515 (prob. E-M293) Prendergast 2019
Pastoral Neolithic PN Tanzania Gishimangeda Cave 2490–2350 L3x1 Prendergast 2019
Pastoral Neolithic PN Kenya Naivasha Burial Site 2350–2210 L3h1a1 E-M293 Prendergast 2019
Pastoral Neolithic PN Kenya Naivasha Burial Site 2320–2150 L3x1a E-M293 Prendergast 2019
Pastoral Neolithic PN Tanzania Gishimangeda Cave 2150–2020 L3i2 E-M293 Prendergast 2019
Pastoral Neolithic or Elmenteitan PN Kenya Njoro River Cave II 2110–1930 L3h1a2a1 Prendergast 2019
Pastoral Neolithic N/A Tanzania Gishimangeda Cave 2000–1900 L3h1a2a1 Prendergast 2019
Pastoral Neolithic PN Kenya Ol Kalou 1810–1620 L3d1d E-M293 Prendergast 2019
Pastoral Iron Age PIA Kenya Kisima Farm, C4 1060–940 L3h1a1 E-M75 (excl. M98) Prendergast 2019
Pastoral Iron Age PIA Kenya Emurua Ole Polos (GvJh122) 420–160 L3h1a1 E-M293 Prendergast 2019
Pastoral Iron Age PN outlier Kenya Kokurmatakore N/A L3a2a E-M35 (not E-M293) Prendergast 2019

Tree edit

This phylogenetic tree of haplogroup L3 subclades is based on the paper by Mannis van Oven and Manfred Kayser Updated comprehensive phylogenetic tree of global human mitochondrial DNA variation[7] and subsequent published research.[41]

Most Recent Common Ancestor (MRCA)

  • L1-6
    • L2-6
      • L2'3'4'6
        • L3'4'6
          • L3'4
            • L3
              • L3a
                • L3a1
                  • L3a1a
                  • L3a1b
                • L3a2
                  • L3a2a
              • L3b'f
                • L3b
                  • L3b1
                    • L3b1a
                      • L3b1a1
                      • L3b1a2
                      • L3b1a3
                      • L3b1a4
                      • L3b1a5
                        • L3b1a5a
                        • L3b1a6
                        • L3b1a7
                          • L3b1a7
                        • L3b1a8
                        • L3b1a9
                          • L3b1a9a
                      • L3b1a10
                      • L3b1a11
                    • L3b1b
                      • L3b1b1
                  • L3b2
                    • L3b2a
                    • L3b2a
                  • L3b3
                • L3f
                  • L3f1
                    • L3f1a
                      • L3f1a1
                    • L3f1b
                      • L3f1b1
                      • L3f1b2
                        • L3f1b2a
                        • L3f1b3
                        • L3f1b4
                          • L3f1b4a
                            • L3f1b4a1
                          • L3f1b4b
                          • L3f1b4c
                      • L3f1b5
                  • L3f2
                    • L3f2a
                    • L3f2b
                  • L3f3
                    • L3f3a
                    • L3f3b
              • L3c'd
                • L3c
                • L3d
                  • L3d1-5
                    • L3d1
                      • L3d1a
                        • L3d1a1
                          • L3d1a1a
                      • L3d1b
                        • L3d1b1
                      • L3d1c
                      • L3d1d
                    • 199
                      • L3d2
                      • L3d5
                    • L3d3
                      • L3d3a
                    • L3d4
                    • L3d5
              • L3e'i'k'x
                • L3e
                  • L3e1
                    • L3e1a
                      • L3e1a1
                        • L3e1a1a
                      • 152
                        • L3e1a2
                        • L3e1a3
                    • L3e1b
                    • L3e1c
                    • L3e1d
                    • L3e1e
                  • L3e2
                    • L3e2a
                      • L3e2a1
                        • L3e2a1a
                        • L3e2a1b
                          • L3e2a1b1
                    • L3e2b
                      • L3e2b1
                        • L3e2b1a
                      • L3e2b2
                      • L3e2b3
                  • L3e3'4'5
                    • L3e3'4
                      • L3e3
                        • L3e3a
                        • L3e3b
                          • L3e3b1
                        • L3e4
                    • L3e5
                • L3i
                  • L3i1
                    • L3i1a
                    • L3i1b
                  • L3i2
                • L3k
                  • L3k1
                • L3x
                  • L3x1
                    • L3x1a
                      • L3x1a1
                      • L3x1a2
                    • L3x1b
                  • L3x2
                    • L3x2a
                      • L3x2a1
                        • L3x2a1a
                    • L3x2b
              • L3h
                • L3h1
                  • L3h1a
                    • L3h1a1
                    • L3h1a2
                      • L3h1a2a
                      • L3h1a2b
                  • L3h1b
                    • L3h1b1
                      • L3h1b1a
                        • L3h1b1a1
                    • L3h1b2
                • L3h2
              • M
              • N

See also edit

Phylogenetic tree of human mitochondrial DNA (mtDNA) haplogroups

  Mitochondrial Eve (L)    
L0 L1–6  
L1 L2   L3     L4 L5 L6
M N  
CZ D E G Q   O A S R   I W X Y
C Z B F R0   pre-JT   P   U
HV JT K
H V J T

References edit

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Notes edit

  1. ^ GUR46 on table 1. is a mtDNA haplogroup L3x2a.

External links edit

haplogroup, human, mitochondrial, mtdna, haplogroup, clade, played, pivotal, role, early, dispersal, anatomically, modern, humans, ancient, dispersal, haplogroup, descendant, lineages, other, mtdna, clades, numbers, represent, thousand, years, before, present,. Haplogroup L3 is a human mitochondrial DNA mtDNA haplogroup The clade has played a pivotal role in the early dispersal of anatomically modern humans Haplogroup L3Ancient dispersal of haplogroup L3 its descendant M and N lineages and other mtDNA clades Numbers represent thousand years before present Possible time of origin80 000 60 000 BP 1 70 000 BP 2 Possible place of originEast Africa 3 4 5 2 or Asia 6 AncestorL3 4DescendantsL3a L3b f L3c d L3e i k x L3h M NDefining mutations769 1018 16311 7 It is strongly associated with the out of Africa migration of modern humans of about 70 50 000 years ago It is inherited by all modern non African populations as well as by some populations in Africa 8 3 Contents 1 Origin 2 Distribution 2 1 Subclade distribution 2 2 Ancient and historic samples 3 Tree 4 See also 5 References 6 Notes 7 External linksOrigin editHaplogroup L3 arose close to 70 000 years ago near the time of the recent out of Africa event This dispersal originated in East Africa and expanded to West Asia and further to South and Southeast Asia in the course of a few millennia and some research suggests that L3 participated in this migration out of Africa A 2007 estimate for the age of L3 suggested a range of 104 84 000 years ago 9 More recent analyses including Soares et al 2012 arrive at a more recent date of roughly 70 60 000 years ago Soares et al also suggest that L3 most likely expanded from East Africa into Eurasia sometime around 65 55 000 years ago as part of the recent out of Africa event as well as from East Africa into Central Africa from 60 to 35 000 years ago 3 In 2016 Soares et al again suggested that haplogroup L3 emerged in East Africa leading to the Out of Africa migration around 70 60 000 years ago 10 Haplogroups L6 and L4 form sister clades of L3 which arose in East Africa at roughly the same time but which did not participate in the out of Africa migration The ancestral clade L3 4 6 has been estimated at 110 kya and the L3 4 clade at 95 kya 8 nbsp Proposed migration route depicting the origin of L3 in Africa and its dispersal both out of and within the continent with two possible models as depicted by Vai et al 4 a Haplogroup N differentiates from L3 in Africa with a subsequent spread out of Africa and differentiation of haplogroup M from L3 outside Africa b Haplogroups M and N diverge from L3 outside Africa after the expansion of L3 from the continent later migrations during the Upper Paleolithic and Neolithic led some lineages back to North Africa Haplogroups are indicated in black circles in their probable area of origin nbsp Proposed migration route according to the Asian origin hypothesis Cabrera et al 6 a Exit of the L3 precursor to Eurasia b Return to Africa and expansion to Asia of basal L3 lineages with subsequent differentiation in both continents The possibility of an origin of L3 in Asia was proposed by Cabrera et al 2018 based on the similar coalescence dates of L3 and its Eurasian distributed M and N derivative clades ca 70 kya the distant location in Southeast Asia of the oldest known subclades of M and N and the comparable age of the paternal haplogroup DE According to this hypothesis after an initial out of Africa migration of bearers of pre L3 L3 4 around 125 kya there would have been a back migration of females carrying L3 from Eurasia to East Africa sometime after 70 kya The hypothesis suggests that this back migration is aligned with bearers of paternal haplogroup E which it also proposes to have originated in Eurasia These new Eurasian lineages are then suggested to have largely replaced the old autochthonous male and female North East African lineages 6 According to other research though earlier migrations out of Africa of anatomically modern humans occurred current Eurasian populations descend instead from a later migration from Africa dated between about 65 000 and 50 000 years ago associated with the migration out of L3 11 4 12 Vai et al 2019 suggest from a newly discovered old and deeply rooted branch of maternal haplogroup N found in early Neolithic North African remains that haplogroup L3 originated in East Africa between 70 000 and 60 000 years ago and both spread within Africa and left Africa as part of the Out of Africa migration with haplogroup N diverging from it soon after between 65 000 and 50 000 years ago either in Arabia or possibly North Africa and haplogroup M originating in the Middle East around the same time as N 4 A study by Lipson et al 2019 analyzing remains from the Cameroonian site of Shum Laka found them to be more similar to modern day Pygmy peoples than to West Africans and suggests that several other groups including the ancestors of West Africans East Africans and the ancestors of non Africans commonly derived from a human population originating in East Africa between about 80 000 60 000 years ago which they suggest was also the source and origin zone of haplogroup L3 around 70 000 years ago 13 Distribution edit nbsp Projected spatial distribution of haplogroup L3 in Africa and the Arabian peninsula L3 is common in Northeast Africa and some other parts of East Africa 14 in contrast to others parts of Africa where the haplogroups L1 and L2 represent around two thirds of mtDNA lineages 15 L3 sublineages are also frequent in the Arabian peninsula L3 is subdivided into several clades two of which spawned the macrohaplogroups M and N that are today carried by most people outside Africa 15 There is at least one relatively deep non M non N clade of L3 outside Africa L3f1b6 which is found at a frequency of 1 in Asturias Spain It diverged from African L3 lineages at least 10 000 years ago 16 According to Maca Meyer et al 2001 L3 is more related to Eurasian haplogroups than to the most divergent African clusters L1 and L2 17 L3 is the haplogroup from which all modern humans outside Africa derive 18 However there is a greater diversity of major L3 branches within Africa than outside of it the two major non African branches being the L3 offshoots M and N Subclade distribution edit nbsp L3 subclade distribution L3b L3d L3e L3f L3h L3i L3x and L3w L3 has seven equidistant descendants L3a L3b f L3c d L3e i k x L3h M N Five are African while two are associated with the Out of Africa event N Eurasia possibly due to migration from Africa and North Africa possibly due to back migration from Eurasia 3 6 4 M Asia the Mediterranean Basin and parts of Africa due to back migration 3 6 L3a East Africa 8 3 Moderate to high frequencies found among the Sanye Samburu Iraqw Yaaku El Molo and other minor indigenous populations from the East African Rift Valley It is infrequent to nonexistent in Sudan and the Sahel zone 19 L3a1 Found across Eastern Africa Estimated age of 35 8 39 3 ka 3 L3a2 Found across Eastern Africa Estimated age of 48 3 57 7 ka 20 L3b f L3b Spread from East Africa in the upper paleolithic to West Central Africa Some subclades spread from Central Africa to East Africa with the Bantu migration 3 L3b1a Common subclade Estimated age of 11 7 14 8 ka 3 L3b1a2 Subclade found in Northeast Africa the Maghreb and Middle East Emerged 12 14 ka 21 20 L3f Northeast Africa Sahel Arabian peninsula Iberia Gaalien 22 Beja 22 L3f1 L3f1a Carried by migrants from Eastern Africa into the Sahel and Central Africa 3 L3f1b Carried by migrants from Eastern Africa into the Sahel and Central Africa 3 L3f1b1 Carried from Central Africa into Southern and Eastern Africa with the Bantu migration 3 L3f1b1a Settled from East Central Africa to Central West Africa and into North Africa and Berber regions 3 L3f1b4 Carried from Central Africa into Southern and Eastern Africa with the Bantu migration 3 L3f1b6 Rare found in Iberia 16 L3f2 Primarily distributed in East Africa 3 Also found in North Africa and Central Africa 21 L3f3 Spread from Eastern Africa to Chad and the Sahel around 8 9 ka 3 Found in the Chad Basin 21 23 L3c d L3c Extremely rare lineage with only two samples found so far in Eastern Africa and the Near East 3 L3d Spread from East Africa in the upper paleolithic to Central Africa Some subclades spread to East Africa with the Bantu migration 3 Found among the Fulani 8 Chadians 8 Ethiopians 24 Akan people 25 Mozambique 24 Yemenites 24 Egyptians Berbers 26 L3d3a1 Primarily found in Southern Africa 20 21 L3e i k x L3e Suggested to have originated in the Central Africa Sudan region about 45 000 years ago during the upper paleolithic period 27 It is the most common L3 sub clade in Bantu speaking populations 28 L3e is also the most common L3 subclade amongst African Americans and Afro Brazilians 29 L3e1 Spread from West Central Africa to Southwest Africa with the Bantu migration Found in Angola 6 8 30 Mozambique Kikuyu of Kenya as well as in Yemen and the Tikar of Cameroon 31 and among the Akan people of Ghana 25 L3e5 Originated in the Chad Basin Found in Algeria 32 as well as Burkina Faso Nigeria South Tunisia South Morocco and Egypt 33 L3i Almost exclusively found in East Africa 3 L3i1 L3i1b Subclade is found in Yemen Ethiopia and among Gujarati Indians 21 L3i2 former L3w Found in the Horn of Africa and Oman 21 L3k Rare haplogroup primarily found in North Africa and the Sahel 3 21 L3x Almost exclusively found in East Africa 3 Found among Ethiopian Oromos 24 Egyptians Note 1 34 L3h Almost exclusively found in East Africa 3 L3h1 Primarily found in East Africa with branches of L3h1b1 sporadically found in the Sahel and North Africa 20 21 L3h2 Found in Northeast Africa and Socotra Split from other L3h branches as early as 65 69 ka during the middle paleolithic 20 21 Ancient and historic samples edit Haplogroup L3 has been observed in an ancient fossil belonging to the Pre Pottery Neolithic B culture 35 L3x2a was observed in a 4 500 year old hunter gather excavated in Mota Ethiopia with the ancient fossil found to be most closely related to modern Southwest Ethiopian populations 36 37 Haplogroup L3 has also been found among ancient Egyptian mummies 1 90 1 excavated at the Abusir el Meleq archaeological site in Middle Egypt with the rest deriving from Eurasian subclades which date from the Pre Ptolemaic late New Kingdom and Ptolemaic periods The Ancient Egyptian mummies bore Near eastern genomic component most closely related to modern near easterners 38 Additionally haplogroup L3 has 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 All of the clade bearing individuals were inhumed at the Gran Canaria site with most of these specimens found to belong to the L3b1a subclade 3 4 75 with the rest from both islands 8 11 72 deriving from Eurasian subclades The Guanche skeletons also bore an autochthonous Maghrebi genomic component that peaks among modern Berbers which suggests that they originated from ancestral Berber populations inhabiting northwestern Affoundnat a high ncy 39 A variety of L3 have been uncovered in ancient remains associated with the Pastoral Neolithic and Pastoral Iron Age of East Africa 40 Culture Genetic cluster or affinity Country Site Date Maternal Haplogroup Paternal Haplogroup SourceEarly pastoral PN Kenya Prettejohn s Gully GsJi11 4060 3860 L3f1b Prendergast 2019Pastoral Neolithic PN Kenya Cole s Burial GrJj5a 3350 3180 L3i2 E V32 Prendergast 2019Pastoral Neolithic or Elmenteitan PN Kenya Rigo Cave GrJh3 2710 2380 L3f E M293 Prendergast 2019Pastoral Neolithic PN Kenya Naishi Rockshelter 2750 2500 L3x1a E V1515 prob E M293 Prendergast 2019Pastoral Neolithic PN Tanzania Gishimangeda Cave 2490 2350 L3x1 Prendergast 2019Pastoral Neolithic PN Kenya Naivasha Burial Site 2350 2210 L3h1a1 E M293 Prendergast 2019Pastoral Neolithic PN Kenya Naivasha Burial Site 2320 2150 L3x1a E M293 Prendergast 2019Pastoral Neolithic PN Tanzania Gishimangeda Cave 2150 2020 L3i2 E M293 Prendergast 2019Pastoral Neolithic or Elmenteitan PN Kenya Njoro River Cave II 2110 1930 L3h1a2a1 Prendergast 2019Pastoral Neolithic N A Tanzania Gishimangeda Cave 2000 1900 L3h1a2a1 Prendergast 2019Pastoral Neolithic PN Kenya Ol Kalou 1810 1620 L3d1d E M293 Prendergast 2019Pastoral Iron Age PIA Kenya Kisima Farm C4 1060 940 L3h1a1 E M75 excl M98 Prendergast 2019Pastoral Iron Age PIA Kenya Emurua Ole Polos GvJh122 420 160 L3h1a1 E M293 Prendergast 2019Pastoral Iron Age PN outlier Kenya Kokurmatakore N A L3a2a E M35 not E M293 Prendergast 2019Tree editThis phylogenetic tree of haplogroup L3 subclades is based on the paper by Mannis van Oven and Manfred Kayser Updated comprehensive phylogenetic tree of global human mitochondrial DNA variation 7 and subsequent published research 41 Most Recent Common Ancestor MRCA L1 6 L2 6 L2 3 4 6 L3 4 6 L3 4 L3 L3a L3a1 L3a1a L3a1b L3a2 L3a2a L3b f L3b L3b1 L3b1a L3b1a1 L3b1a2 L3b1a3 L3b1a4 L3b1a5 L3b1a5a L3b1a6 L3b1a7 L3b1a7 L3b1a8 L3b1a9 L3b1a9a L3b1a10 L3b1a11 L3b1b L3b1b1 L3b2 L3b2a L3b2a L3b3 L3f L3f1 L3f1a L3f1a1 L3f1b L3f1b1 L3f1b2 L3f1b2a L3f1b3 L3f1b4 L3f1b4a L3f1b4a1 L3f1b4b L3f1b4c L3f1b5 L3f2 L3f2a L3f2b L3f3 L3f3a L3f3b L3c d L3c L3d L3d1 5 L3d1 L3d1a L3d1a1 L3d1a1a L3d1b L3d1b1 L3d1c L3d1d 199 L3d2 L3d5 L3d3 L3d3a L3d4 L3d5 L3e i k x L3e L3e1 L3e1a L3e1a1 L3e1a1a 152 L3e1a2 L3e1a3 L3e1b L3e1c L3e1d L3e1e L3e2 L3e2a L3e2a1 L3e2a1a L3e2a1b L3e2a1b1 L3e2b L3e2b1 L3e2b1a L3e2b2 L3e2b3 L3e3 4 5 L3e3 4 L3e3 L3e3a L3e3b L3e3b1 L3e4 L3e5 L3i L3i1 L3i1a L3i1b L3i2 L3k L3k1 L3x L3x1 L3x1a L3x1a1 L3x1a2 L3x1b L3x2 L3x2a L3x2a1 L3x2a1a L3x2b L3h L3h1 L3h1a L3h1a1 L3h1a2 L3h1a2a L3h1a2b L3h1b L3h1b1 L3h1b1a L3h1b1a1 L3h1b2 L3h2 M NSee also edit nbsp Wikimedia Commons has media related to Haplogroup L3 mtDNA Genealogical DNA test Genetic genealogy Haplogroup Population geneticsPhylogenetic tree of human mitochondrial DNA mtDNA haplogroups Mitochondrial Eve L L0 L1 6 L1 L2 L3 L4 L5 L6M N CZ D E G Q O A S R I W X YC Z B F R0 pre JT P UHV JT KH V J TReferences edit Soares et al 2011 Point estimates of 71 6 kya by Soares et al 2009 and of 70 2 by Fernandes et al 2015 a b Lipson Mark et al 22 January 2020 Ancient West African foragers in the context of African population history Nature 577 7792 665 669 Bibcode 2020Natur 577 665L doi 10 1038 s41586 020 1929 1 ISSN 0028 0836 OCLC 8545173694 PMC 8386425 PMID 31969706 S2CID 210862788 a b c d e f g h i j k l m n o p q r s t u v Soares P Alshamali F Pereira J B Fernandes V Silva N M Afonso C Costa M D Musilova E Macaulay V 2011 11 16 The Expansion of mtDNA Haplogroup L3 within and out of Africa Molecular Biology and Evolution 29 3 915 927 CiteSeerX 10 1 1 923 345 doi 10 1093 molbev msr245 ISSN 0737 4038 PMID 22096215 a b c d e Vai S Sarno S Lari M Luiselli D Manzi G Gallinaro M Mataich S Hubner A Modi A Pilli E Tafuri MA Caramelli D di Lernia S March 2019 Ancestral mitochondrial N lineage from the Neolithic green Sahara Sci Rep 9 1 3530 Bibcode 2019NatSR 9 3530V doi 10 1038 s41598 019 39802 1 PMC 6401177 PMID 30837540 Osman Maha M et al Mitochondrial HVRI and whole mitogenome 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Reed F A De Sousa A Tishkoff S A 2006 Whole mtDNA Genome Sequence Analysis of Ancient African Lineages Molecular Biology and Evolution 24 3 757 68 doi 10 1093 molbev msl209 PMID 17194802 Soares P Rito T Pereira L Richards M March 2016 A Genetic Perspective on African Prehistory PDF Africa from MIS 6 2 Vertebrate Paleobiology and Paleoanthropology pp 383 405 doi 10 1007 978 94 017 7520 5 18 ISBN 978 94 017 7519 9 S2CID 26196645 Posth C Renaud G Mittnik M Drucker DG Rougier H Cupillard C Valentin F Thevenet C Furtwangler A Wissing C Francken M Malina M Bolus M Lari M Gigli E Capecchi G Crevecoeur I Beauval C Flas D Germonpre M van der Plicht J Cottiaux R Gely B Ronchitelli A Wehrberger K Grigorescu D Svoboda J Semal P Caramelli D Bocherens H Harvati K Conard NJ Haak W Powell A Krause J 2016 Pleistocene Mitochondrial Genomes Suggest a Single Major Dispersal of Non Africans and a Late Glacial Population Turnover in Europe Current Biology 26 6 827 833 doi 10 1016 j cub 2016 01 037 hdl 2440 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Llorente M Gallego Jones E R Eriksson A Siska V Arthur K W Arthur J W Curtis M C Stock J T Coltorti M Pieruccini P Stretton S Brock F Higham T Park Y Hofreiter M Bradley D G Bhak J Pinhasi R Manica A 13 November 2015 Ancient Ethiopian genome reveals extensive Eurasian admixture in Eastern Africa Science 350 6262 820 822 Bibcode 2015Sci 350 820L doi 10 1126 science aad2879 hdl 2318 1661894 PMID 26449472 Llorente M Gallego Jones E R Eriksson A Siska V Arthur K W Arthur J W Curtis M C Stock J T Coltorti M 2015 11 13 Ancient Ethiopian genome reveals extensive Eurasian admixture in Eastern Africa Science 350 6262 820 822 Bibcode 2015Sci 350 820L doi 10 1126 science aad2879 hdl 2318 1661894 PMID 26449472 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 Rodriguez 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 Prendergast Mary E Lipson Mark Sawchuk Elizabeth A Olalde Inigo Ogola Christine A Rohland Nadin Sirak Kendra A Adamski Nicole Bernardos Rebecca 2019 05 30 Ancient DNA reveals a multistep spread of the first herders into sub Saharan Africa Science 365 6448 eaaw6275 Bibcode 2019Sci 365 6275P doi 10 1126 science aaw6275 ISSN 0036 8075 PMC 6827346 PMID 31147405 PhyloTree org tree L3 phylotree org Retrieved 2018 06 25 Notes edit GUR46 on table 1 is a mtDNA haplogroup L3x2a External links editGeneral Ian Logan s Mitochondrial DNA Site Haplogroup L3 Mannis van Oven s PhyloTree org mtDNA subtree L3 Spread of Haplogroup L3 from National Geographic Retrieved from https en wikipedia org w index php title Haplogroup L3 amp oldid 1200069092, wikipedia, wiki, book, books, library,

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