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Mitochondrial lineage M1 traces an early human backflow to Africa

BACKGROUND: The out of Africa hypothesis has gained generalized consensus. However, many specific questions remain unsettled. To know whether the two M and N macrohaplogroups that colonized Eurasia were already present in Africa before the exit is puzzling. It has been proposed that the east African...

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Autores principales: González, Ana M, Larruga, José M, Abu-Amero, Khaled K, Shi, Yufei, Pestano, José, Cabrera, Vicente M
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1945034/
https://www.ncbi.nlm.nih.gov/pubmed/17620140
http://dx.doi.org/10.1186/1471-2164-8-223
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author González, Ana M
Larruga, José M
Abu-Amero, Khaled K
Shi, Yufei
Pestano, José
Cabrera, Vicente M
author_facet González, Ana M
Larruga, José M
Abu-Amero, Khaled K
Shi, Yufei
Pestano, José
Cabrera, Vicente M
author_sort González, Ana M
collection PubMed
description BACKGROUND: The out of Africa hypothesis has gained generalized consensus. However, many specific questions remain unsettled. To know whether the two M and N macrohaplogroups that colonized Eurasia were already present in Africa before the exit is puzzling. It has been proposed that the east African clade M1 supports a single origin of haplogroup M in Africa. To test the validity of that hypothesis, the phylogeographic analysis of 13 complete mitochondrial DNA (mtDNA) sequences and 261 partial sequences belonging to haplogroup M1 was carried out. RESULTS: The coalescence age of the African haplogroup M1 is younger than those for other M Asiatic clades. In contradiction to the hypothesis of an eastern Africa origin for modern human expansions out of Africa, the most ancestral M1 lineages have been found in Northwest Africa and in the Near East, instead of in East Africa. The M1 geographic distribution and the relative ages of its different subclades clearly correlate with those of haplogroup U6, for which an Eurasian ancestor has been demonstrated. CONCLUSION: This study provides evidence that M1, or its ancestor, had an Asiatic origin. The earliest M1 expansion into Africa occurred in northwestern instead of eastern areas; this early spread reached the Iberian Peninsula even affecting the Basques. The majority of the M1a lineages found outside and inside Africa had a more recent eastern Africa origin. Both western and eastern M1 lineages participated in the Neolithic colonization of the Sahara. The striking parallelism between subclade ages and geographic distribution of M1 and its North African U6 counterpart strongly reinforces this scenario. Finally, a relevant fraction of M1a lineages present today in the European Continent and nearby islands possibly had a Jewish instead of the commonly proposed Arab/Berber maternal ascendance.
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spelling pubmed-19450342007-08-11 Mitochondrial lineage M1 traces an early human backflow to Africa González, Ana M Larruga, José M Abu-Amero, Khaled K Shi, Yufei Pestano, José Cabrera, Vicente M BMC Genomics Research Article BACKGROUND: The out of Africa hypothesis has gained generalized consensus. However, many specific questions remain unsettled. To know whether the two M and N macrohaplogroups that colonized Eurasia were already present in Africa before the exit is puzzling. It has been proposed that the east African clade M1 supports a single origin of haplogroup M in Africa. To test the validity of that hypothesis, the phylogeographic analysis of 13 complete mitochondrial DNA (mtDNA) sequences and 261 partial sequences belonging to haplogroup M1 was carried out. RESULTS: The coalescence age of the African haplogroup M1 is younger than those for other M Asiatic clades. In contradiction to the hypothesis of an eastern Africa origin for modern human expansions out of Africa, the most ancestral M1 lineages have been found in Northwest Africa and in the Near East, instead of in East Africa. The M1 geographic distribution and the relative ages of its different subclades clearly correlate with those of haplogroup U6, for which an Eurasian ancestor has been demonstrated. CONCLUSION: This study provides evidence that M1, or its ancestor, had an Asiatic origin. The earliest M1 expansion into Africa occurred in northwestern instead of eastern areas; this early spread reached the Iberian Peninsula even affecting the Basques. The majority of the M1a lineages found outside and inside Africa had a more recent eastern Africa origin. Both western and eastern M1 lineages participated in the Neolithic colonization of the Sahara. The striking parallelism between subclade ages and geographic distribution of M1 and its North African U6 counterpart strongly reinforces this scenario. Finally, a relevant fraction of M1a lineages present today in the European Continent and nearby islands possibly had a Jewish instead of the commonly proposed Arab/Berber maternal ascendance. BioMed Central 2007-07-09 /pmc/articles/PMC1945034/ /pubmed/17620140 http://dx.doi.org/10.1186/1471-2164-8-223 Text en Copyright © 2007 González et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
González, Ana M
Larruga, José M
Abu-Amero, Khaled K
Shi, Yufei
Pestano, José
Cabrera, Vicente M
Mitochondrial lineage M1 traces an early human backflow to Africa
title Mitochondrial lineage M1 traces an early human backflow to Africa
title_full Mitochondrial lineage M1 traces an early human backflow to Africa
title_fullStr Mitochondrial lineage M1 traces an early human backflow to Africa
title_full_unstemmed Mitochondrial lineage M1 traces an early human backflow to Africa
title_short Mitochondrial lineage M1 traces an early human backflow to Africa
title_sort mitochondrial lineage m1 traces an early human backflow to africa
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1945034/
https://www.ncbi.nlm.nih.gov/pubmed/17620140
http://dx.doi.org/10.1186/1471-2164-8-223
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