Numerous population samples from around the world have been tested for Y chromosome–specific p49a,f/TaqI restriction polymorphisms. Here we review the literature as well as unpublished data on Y-chromosome p49a,f/ TaqI haplotypes and provide a new nomenclature unifying the notations used by different laboratories.We use this large data set to study worldwide genetic variability of human populations for this paternally transmitted chromosome segment. We observe, for the Y chromosome, an important level of population genetic structure among human populations (FST 5 .230, P ! .001), mainly due to genetic differences among distinct linguistic groups of populations (F 5 .246, P ! .001). CT A multivariate analysis based on genetic distances between populations shows that human population structure inferred from the Y chromosome corresponds broadly to language families (r 5 .567, P ! .001), in agreement with autosomal and mitochondrial data. Times of divergence of linguistic families, estimated from their internal level of genetic differentiation, are fairly concordant with current archaeological and linguistic hypotheses. Variability of the p49a,f/TaqI polymorphic marker is also significantly correlated with the geographic location of the populations (r 5 .613, P ! .001), reflecting the fact that distinct linguistic groups generally also occupy distinct geographic areas. Comparison of Y-chromosome and mtDNA RFLPs in a restricted set of populations shows a globally high level of congruence, but it also allows identification of unequal maternal and paternal contributions to the gene pool of several populations.

Human genetic affinities for Y-chromosome P49a,f/TaqI haplotypes show strong correspondence with linguistics.

SEMINO, ORNELLA;BENERECETTI, AUGUSTA SILVANA;
1997-01-01

Abstract

Numerous population samples from around the world have been tested for Y chromosome–specific p49a,f/TaqI restriction polymorphisms. Here we review the literature as well as unpublished data on Y-chromosome p49a,f/ TaqI haplotypes and provide a new nomenclature unifying the notations used by different laboratories.We use this large data set to study worldwide genetic variability of human populations for this paternally transmitted chromosome segment. We observe, for the Y chromosome, an important level of population genetic structure among human populations (FST 5 .230, P ! .001), mainly due to genetic differences among distinct linguistic groups of populations (F 5 .246, P ! .001). CT A multivariate analysis based on genetic distances between populations shows that human population structure inferred from the Y chromosome corresponds broadly to language families (r 5 .567, P ! .001), in agreement with autosomal and mitochondrial data. Times of divergence of linguistic families, estimated from their internal level of genetic differentiation, are fairly concordant with current archaeological and linguistic hypotheses. Variability of the p49a,f/TaqI polymorphic marker is also significantly correlated with the geographic location of the populations (r 5 .613, P ! .001), reflecting the fact that distinct linguistic groups generally also occupy distinct geographic areas. Comparison of Y-chromosome and mtDNA RFLPs in a restricted set of populations shows a globally high level of congruence, but it also allows identification of unequal maternal and paternal contributions to the gene pool of several populations.
1997
Molecular Biology & Genetics considers all aspects of basic and applied genetics, including molecular genetics, prokaryotic and eukaryotic gene expression, mechanisms of mutagenesis, structure, function and regulation of genetic material. Also included are resources concerned with clinical genetics, patterns of inheritance, genetic cause, and screening and treatment of disease. Resources dealing specifically with developmentally regulated gene expression, or with signal transduction pathways that modulate gene expression at the cellular level are excluded and are covered in the Cell and Developmental Biology category.
Esperti anonimi
Inglese
Internazionale
STAMPA
61
5
1015
1035
21
Y CHROMOSOME; MITOCHONDRIAL DNA; HUMAN GENETIC HISTORY.
http://www.sciencedirect.com/science/article/pii/S0002929707601918
7
info:eu-repo/semantics/article
262
Poloni, Es; Semino, Ornella; Passarino, G; Benerecetti, AUGUSTA SILVANA; Dupanloup, I; Langaney, A; Excoffier, L.
1 Contributo su Rivista::1.1 Articolo in rivista
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/133271
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