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Proc Natl Acad Sci U S A ; 109(22): 8471-6, 2012 May 29.
Artigo em Inglês | MEDLINE | ID: mdl-22586127

RESUMO

For decades, the peopling of the Americas has been explored through the analysis of uniparentally inherited genetic systems in Native American populations and the comparison of these genetic data with current linguistic groupings. In northern North America, two language families predominate: Eskimo-Aleut and Na-Dene. Although the genetic evidence from nuclear and mtDNA loci suggest that speakers of these language families share a distinct biological origin, this model has not been examined using data from paternally inherited Y chromosomes. To test this hypothesis and elucidate the migration histories of Eskimoan- and Athapaskan-speaking populations, we analyzed Y-chromosomal data from Inuvialuit, Gwich'in, and Tlich populations living in the Northwest Territories of Canada. Over 100 biallelic markers and 19 chromosome short tandem repeats (STRs) were genotyped to produce a high-resolution dataset of Y chromosomes from these groups. Among these markers is an SNP discovered in the Inuvialuit that differentiates them from other Aboriginal and Native American populations. The data suggest that Canadian Eskimoan- and Athapaskan-speaking populations are genetically distinct from one another and that the formation of these groups was the result of two population expansions that occurred after the initial movement of people into the Americas. In addition, the population history of Athapaskan speakers is complex, with the Tlich being distinct from other Athapaskan groups. The high-resolution biallelic data also make clear that Y-chromosomal diversity among the first Native Americans was greater than previously recognized.


Assuntos
Cromossomos Humanos Y/genética , Variação Genética , Indígenas Norte-Americanos/genética , Inuíte/genética , Filogenia , Canadá , Cromossomos Humanos Par 19/genética , Emigração e Imigração , Frequência do Gene , Genética Populacional/métodos , Genótipo , Geografia , Haplótipos/genética , Humanos , Masculino , Repetições de Microssatélites/genética , Mutação , Taxa de Mutação , Polimorfismo de Nucleotídeo Único
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