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Ancestral Components of Admixed Genomes in a Mexican Cohort

For most of the world, human genome structure at a population level is shaped by interplay between ancient geographic isolation and more recent demographic shifts, factors that are captured by the concepts of biogeographic ancestry and admixture, respectively. The ancestry of non-admixed individuals...

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Autores principales: Johnson, Nicholas A., Coram, Marc A., Shriver, Mark D., Romieu, Isabelle, Barsh, Gregory S., London, Stephanie J., Tang, Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3240599/
https://www.ncbi.nlm.nih.gov/pubmed/22194699
http://dx.doi.org/10.1371/journal.pgen.1002410
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author Johnson, Nicholas A.
Coram, Marc A.
Shriver, Mark D.
Romieu, Isabelle
Barsh, Gregory S.
London, Stephanie J.
Tang, Hua
author_facet Johnson, Nicholas A.
Coram, Marc A.
Shriver, Mark D.
Romieu, Isabelle
Barsh, Gregory S.
London, Stephanie J.
Tang, Hua
author_sort Johnson, Nicholas A.
collection PubMed
description For most of the world, human genome structure at a population level is shaped by interplay between ancient geographic isolation and more recent demographic shifts, factors that are captured by the concepts of biogeographic ancestry and admixture, respectively. The ancestry of non-admixed individuals can often be traced to a specific population in a precise region, but current approaches for studying admixed individuals generally yield coarse information in which genome ancestry proportions are identified according to continent of origin. Here we introduce a new analytic strategy for this problem that allows fine-grained characterization of admixed individuals with respect to both geographic and genomic coordinates. Ancestry segments from different continents, identified with a probabilistic model, are used to construct and study “virtual genomes” of admixed individuals. We apply this approach to a cohort of 492 parent–offspring trios from Mexico City. The relative contributions from the three continental-level ancestral populations—Africa, Europe, and America—vary substantially between individuals, and the distribution of haplotype block length suggests an admixing time of 10–15 generations. The European and Indigenous American virtual genomes of each Mexican individual can be traced to precise regions within each continent, and they reveal a gradient of Amerindian ancestry between indigenous people of southwestern Mexico and Mayans of the Yucatan Peninsula. This contrasts sharply with the African roots of African Americans, which have been characterized by a uniform mixing of multiple West African populations. We also use the virtual European and Indigenous American genomes to search for the signatures of selection in the ancestral populations, and we identify previously known targets of selection in other populations, as well as new candidate loci. The ability to infer precise ancestral components of admixed genomes will facilitate studies of disease-related phenotypes and will allow new insight into the adaptive and demographic history of indigenous people.
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spelling pubmed-32405992011-12-22 Ancestral Components of Admixed Genomes in a Mexican Cohort Johnson, Nicholas A. Coram, Marc A. Shriver, Mark D. Romieu, Isabelle Barsh, Gregory S. London, Stephanie J. Tang, Hua PLoS Genet Research Article For most of the world, human genome structure at a population level is shaped by interplay between ancient geographic isolation and more recent demographic shifts, factors that are captured by the concepts of biogeographic ancestry and admixture, respectively. The ancestry of non-admixed individuals can often be traced to a specific population in a precise region, but current approaches for studying admixed individuals generally yield coarse information in which genome ancestry proportions are identified according to continent of origin. Here we introduce a new analytic strategy for this problem that allows fine-grained characterization of admixed individuals with respect to both geographic and genomic coordinates. Ancestry segments from different continents, identified with a probabilistic model, are used to construct and study “virtual genomes” of admixed individuals. We apply this approach to a cohort of 492 parent–offspring trios from Mexico City. The relative contributions from the three continental-level ancestral populations—Africa, Europe, and America—vary substantially between individuals, and the distribution of haplotype block length suggests an admixing time of 10–15 generations. The European and Indigenous American virtual genomes of each Mexican individual can be traced to precise regions within each continent, and they reveal a gradient of Amerindian ancestry between indigenous people of southwestern Mexico and Mayans of the Yucatan Peninsula. This contrasts sharply with the African roots of African Americans, which have been characterized by a uniform mixing of multiple West African populations. We also use the virtual European and Indigenous American genomes to search for the signatures of selection in the ancestral populations, and we identify previously known targets of selection in other populations, as well as new candidate loci. The ability to infer precise ancestral components of admixed genomes will facilitate studies of disease-related phenotypes and will allow new insight into the adaptive and demographic history of indigenous people. Public Library of Science 2011-12-15 /pmc/articles/PMC3240599/ /pubmed/22194699 http://dx.doi.org/10.1371/journal.pgen.1002410 Text en This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication. https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Johnson, Nicholas A.
Coram, Marc A.
Shriver, Mark D.
Romieu, Isabelle
Barsh, Gregory S.
London, Stephanie J.
Tang, Hua
Ancestral Components of Admixed Genomes in a Mexican Cohort
title Ancestral Components of Admixed Genomes in a Mexican Cohort
title_full Ancestral Components of Admixed Genomes in a Mexican Cohort
title_fullStr Ancestral Components of Admixed Genomes in a Mexican Cohort
title_full_unstemmed Ancestral Components of Admixed Genomes in a Mexican Cohort
title_short Ancestral Components of Admixed Genomes in a Mexican Cohort
title_sort ancestral components of admixed genomes in a mexican cohort
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3240599/
https://www.ncbi.nlm.nih.gov/pubmed/22194699
http://dx.doi.org/10.1371/journal.pgen.1002410
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