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A Worldwide Phylogeography for the Human X Chromosome

BACKGROUND: We reasoned that by identifying genetic markers on human X chromosome regions where recombination is rare or absent, we should be able to construct X chromosome genealogies analogous to those based on Y chromosome and mitochondrial DNA polymorphisms, with the advantage of providing infor...

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Autores principales: Santos-Lopes, Simone S., Pereira, Rinaldo W., Wilson, Ian J., Pena, Sérgio D.J.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1891433/
https://www.ncbi.nlm.nih.gov/pubmed/17593958
http://dx.doi.org/10.1371/journal.pone.0000557
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author Santos-Lopes, Simone S.
Pereira, Rinaldo W.
Wilson, Ian J.
Pena, Sérgio D.J.
author_facet Santos-Lopes, Simone S.
Pereira, Rinaldo W.
Wilson, Ian J.
Pena, Sérgio D.J.
author_sort Santos-Lopes, Simone S.
collection PubMed
description BACKGROUND: We reasoned that by identifying genetic markers on human X chromosome regions where recombination is rare or absent, we should be able to construct X chromosome genealogies analogous to those based on Y chromosome and mitochondrial DNA polymorphisms, with the advantage of providing information about both male and female components of the population. METHODOLOGY/PRINCIPAL FINDINGS: We identified a 47 Kb interval containing an Alu insertion polymorphism (DXS225) and four microsatellites in complete linkage disequilibrium in a low recombination rate region of the long arm of the human X chromosome. This haplotype block was studied in 667 males from the HGDP-CEPH Human Genome Diversity Panel. The haplotypic diversity was highest in Africa (0.992±0.0025) and lowest in the Americas (0.839±0.0378), where no insertion alleles of DXS225 were observed. Africa shared few haplotypes with other geographical areas, while those exhibited significant sharing among themselves. Median joining networks revealed that the African haplotypes were numerous, occupied the periphery of the graph and had low frequency, whereas those from the other continents were few, central and had high frequency. Altogether, our data support a single origin of modern man in Africa and migration to occupy the other continents by serial founder effects. Coalescent analysis permitted estimation of the time of the most recent common ancestor as 182,000 years (56,700–479,000) and the estimated time of the DXS225 Alu insertion of 94,400 years (24,300–310,000). These dates are fully compatible with the current widely accepted scenario of the origin of modern mankind in Africa within the last 195,000 years and migration out-of-Africa circa 55,000–65,000 years ago. CONCLUSIONS/SIGNIFICANCE: A haplotypic block combining an Alu insertion polymorphism and four microsatellite markers on the human X chromosome is a useful marker to evaluate genetic diversity of human populations and provides a highly informative tool for evolutionary studies.
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spelling pubmed-18914332007-06-27 A Worldwide Phylogeography for the Human X Chromosome Santos-Lopes, Simone S. Pereira, Rinaldo W. Wilson, Ian J. Pena, Sérgio D.J. PLoS One Research Article BACKGROUND: We reasoned that by identifying genetic markers on human X chromosome regions where recombination is rare or absent, we should be able to construct X chromosome genealogies analogous to those based on Y chromosome and mitochondrial DNA polymorphisms, with the advantage of providing information about both male and female components of the population. METHODOLOGY/PRINCIPAL FINDINGS: We identified a 47 Kb interval containing an Alu insertion polymorphism (DXS225) and four microsatellites in complete linkage disequilibrium in a low recombination rate region of the long arm of the human X chromosome. This haplotype block was studied in 667 males from the HGDP-CEPH Human Genome Diversity Panel. The haplotypic diversity was highest in Africa (0.992±0.0025) and lowest in the Americas (0.839±0.0378), where no insertion alleles of DXS225 were observed. Africa shared few haplotypes with other geographical areas, while those exhibited significant sharing among themselves. Median joining networks revealed that the African haplotypes were numerous, occupied the periphery of the graph and had low frequency, whereas those from the other continents were few, central and had high frequency. Altogether, our data support a single origin of modern man in Africa and migration to occupy the other continents by serial founder effects. Coalescent analysis permitted estimation of the time of the most recent common ancestor as 182,000 years (56,700–479,000) and the estimated time of the DXS225 Alu insertion of 94,400 years (24,300–310,000). These dates are fully compatible with the current widely accepted scenario of the origin of modern mankind in Africa within the last 195,000 years and migration out-of-Africa circa 55,000–65,000 years ago. CONCLUSIONS/SIGNIFICANCE: A haplotypic block combining an Alu insertion polymorphism and four microsatellite markers on the human X chromosome is a useful marker to evaluate genetic diversity of human populations and provides a highly informative tool for evolutionary studies. Public Library of Science 2007-06-27 /pmc/articles/PMC1891433/ /pubmed/17593958 http://dx.doi.org/10.1371/journal.pone.0000557 Text en Santos-Lopes et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Santos-Lopes, Simone S.
Pereira, Rinaldo W.
Wilson, Ian J.
Pena, Sérgio D.J.
A Worldwide Phylogeography for the Human X Chromosome
title A Worldwide Phylogeography for the Human X Chromosome
title_full A Worldwide Phylogeography for the Human X Chromosome
title_fullStr A Worldwide Phylogeography for the Human X Chromosome
title_full_unstemmed A Worldwide Phylogeography for the Human X Chromosome
title_short A Worldwide Phylogeography for the Human X Chromosome
title_sort worldwide phylogeography for the human x chromosome
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1891433/
https://www.ncbi.nlm.nih.gov/pubmed/17593958
http://dx.doi.org/10.1371/journal.pone.0000557
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