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Genetic Heterogeneity in Algerian Human Populations.

Identifieur interne : 000003 ( PubMed/Corpus ); précédent : 000002; suivant : 000004

Genetic Heterogeneity in Algerian Human Populations.

Auteurs : Asmahan Bekada ; Lara R. Arauna ; Tahria Deba ; Francesc Calafell ; Soraya Benhamamouch ; David Comas

Source :

RBID : pubmed:26402429

English descriptors

Abstract

The demographic history of human populations in North Africa has been characterized by complex processes of admixture and isolation that have modeled its current gene pool. Diverse genetic ancestral components with different origins (autochthonous, European, Middle Eastern, and sub-Saharan) and genetic heterogeneity in the region have been described. In this complex genetic landscape, Algeria, the largest country in Africa, has been poorly covered, with most of the studies using a single Algerian sample. In order to evaluate the genetic heterogeneity of Algeria, Y-chromosome, mtDNA and autosomal genome-wide makers have been analyzed in several Berber- and Arab-speaking groups. Our results show that the genetic heterogeneity found in Algeria is not correlated with geography or linguistics, challenging the idea of Berber groups being genetically isolated and Arab groups open to gene flow. In addition, we have found that external sources of gene flow into North Africa have been carried more often by females than males, while the North African autochthonous component is more frequent in paternally transmitted genome regions. Our results highlight the different demographic history revealed by different markers and urge to be cautious when deriving general conclusions from partial genomic information or from single samples as representatives of the total population of a region.

DOI: 10.1371/journal.pone.0138453
PubMed: 26402429

Links to Exploration step

pubmed:26402429

Le document en format XML

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<CommentsCorrectionsList>
<CommentsCorrections RefType="Cites">
<RefSource>Ann Hum Genet. 1996 Jul;60(Pt 4):331-50</RefSource>
<PMID Version="1">8865993</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Am J Hum Genet. 2008 Nov;83(5):633-42</RefSource>
<PMID Version="1">18976729</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Nat Genet. 1999 Oct;23(2):147</RefSource>
<PMID Version="1">10508508</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Hum Mutat. 2009 Feb;30(2):E386-94</RefSource>
<PMID Version="1">18853457</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Ann Hum Genet. 2009 Mar;73(2):196-214</RefSource>
<PMID Version="1">19053990</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>BMC Genet. 2009;10:8</RefSource>
<PMID Version="1">19243582</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Genome Res. 2009 Sep;19(9):1655-64</RefSource>
<PMID Version="1">19648217</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Mol Biol Evol. 2010 Feb;27(2):385-93</RefSource>
<PMID Version="1">19822636</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>BMC Evol Biol. 2010;10:138</RefSource>
<PMID Version="1">20459715</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Eur J Hum Genet. 2010 Aug;18(8):915-23</RefSource>
<PMID Version="1">20234393</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>PLoS One. 2010;5(10):e13378</RefSource>
<PMID Version="1">20975840</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Proc Natl Acad Sci U S A. 1989 Dec;86(23):9350-4</RefSource>
<PMID Version="1">2594772</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Nat Genet. 2006 Aug;38(8):904-9</RefSource>
<PMID Version="1">16862161</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Science. 2006 Dec 15;314(5806):1767-70</RefSource>
<PMID Version="1">17170302</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Proc Natl Acad Sci U S A. 2007 Apr 10;104(15):6128-33</RefSource>
<PMID Version="1">17372199</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Mol Biol Evol. 2007 Jun;24(6):1300-11</RefSource>
<PMID Version="1">17351267</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>PLoS Genet. 2006 Dec;2(12):e190</RefSource>
<PMID Version="1">17194218</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>PLoS Genet. 2007 Jun;3(6):e104</RefSource>
<PMID Version="1">17604454</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>BMC Genomics. 2007;8:223</RefSource>
<PMID Version="1">17620140</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Am J Hum Genet. 2007 Sep;81(3):559-75</RefSource>
<PMID Version="1">17701901</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Science. 2008 Feb 22;319(5866):1100-4</RefSource>
<PMID Version="1">18292342</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Int J Legal Med. 2008 May;122(3):251-5</RefSource>
<PMID Version="1">17909833</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Ann Hum Genet. 2003 Jul;67(Pt 4):312-28</RefSource>
<PMID Version="1">12914566</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Am J Hum Genet. 2004 May;74(5):1023-34</RefSource>
<PMID Version="1">15069642</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Am J Phys Anthropol. 2011 May;145(1):107-17</RefSource>
<PMID Version="1">21312180</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>J Hum Genet. 2011 Oct;56(10):734-41</RefSource>
<PMID Version="1">21833004</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>PLoS Genet. 2012 Jan;8(1):e1002397</RefSource>
<PMID Version="1">22253600</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Mol Biol Evol. 2012 Sep;29(9):2211-22</RefSource>
<PMID Version="1">22411853</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>PLoS One. 2013;8(2):e56775</RefSource>
<PMID Version="1">23431392</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Nat Commun. 2013;4:1764</RefSource>
<PMID Version="1">23612305</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>PLoS One. 2013;8(11):e80293</RefSource>
<PMID Version="1">24312208</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>BMC Evol Biol. 2014;14:109</RefSource>
<PMID Version="1">24885141</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>J Hum Genet. 2015 Jan;60(1):41-9</RefSource>
<PMID Version="1">25471516</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Eur J Hum Genet. 2000 May;8(5):360-6</RefSource>
<PMID Version="1">10854096</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Hum Genet. 2000 Oct;107(4):312-9</RefSource>
<PMID Version="1">11129330</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Genome Res. 2008 May;18(5):830-8</RefSource>
<PMID Version="1">18385274</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Nucleic Acids Res. 1988 Feb 11;16(3):1215</RefSource>
<PMID Version="1">3344216</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Am J Hum Genet. 2001 Apr;68(4):1019-29</RefSource>
<PMID Version="1">11254456</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Science. 2002 Apr 12;296(5566):261-2</RefSource>
<PMID Version="1">11954565</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Ann Hum Genet. 2004 May;68(Pt 3):222-33</RefSource>
<PMID Version="1">15180702</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Am J Hum Genet. 2004 Aug;75(2):338-45</RefSource>
<PMID Version="1">15202071</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Hum Biol. 1997 Jun;69(3):295-311</RefSource>
<PMID Version="1">9164042</PMID>
</CommentsCorrections>
</CommentsCorrectionsList>
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