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Computer simulation of human leukocyte antigen genes supports two main routes of colonization by human populations in East Asia

BACKGROUND: Recent genetic studies have suggested that the colonization of East Asia by modern humans was more complex than a single origin from the South, and that a genetic contribution via a Northern route was probably quite substantial. RESULTS: Here we use a spatially-explicit computer simulati...

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Autores principales: Di, Da, Sanchez-Mazas, Alicia, Currat, Mathias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4632674/
https://www.ncbi.nlm.nih.gov/pubmed/26530905
http://dx.doi.org/10.1186/s12862-015-0512-0
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author Di, Da
Sanchez-Mazas, Alicia
Currat, Mathias
author_facet Di, Da
Sanchez-Mazas, Alicia
Currat, Mathias
author_sort Di, Da
collection PubMed
description BACKGROUND: Recent genetic studies have suggested that the colonization of East Asia by modern humans was more complex than a single origin from the South, and that a genetic contribution via a Northern route was probably quite substantial. RESULTS: Here we use a spatially-explicit computer simulation approach to investigate the human migration hypotheses of this region based on one-route or two-route models. We test the likelihood of each scenario by using Human Leukocyte Antigen (HLA) − A, −B, and − DRB1 genetic data of East Asian populations, with both selective and demographic parameters considered. The posterior distribution of each parameter is estimated by an Approximate Bayesian Computation (ABC) approach. CONCLUSIONS: Our results strongly support a model with two main routes of colonization of East Asia on both sides of the Himalayas, with distinct demographic histories in Northern and Southern populations, characterized by more isolation in the South. In East Asia, gene flow between populations originating from the two routes probably existed until a remote prehistoric period, explaining the continuous pattern of genetic variation currently observed along the latitude. A significant although dissimilar level of balancing selection acting on the three HLA loci is detected, but its effect on the local genetic patterns appears to be minor compared to those of past demographic events. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12862-015-0512-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-46326742015-11-05 Computer simulation of human leukocyte antigen genes supports two main routes of colonization by human populations in East Asia Di, Da Sanchez-Mazas, Alicia Currat, Mathias BMC Evol Biol Research Article BACKGROUND: Recent genetic studies have suggested that the colonization of East Asia by modern humans was more complex than a single origin from the South, and that a genetic contribution via a Northern route was probably quite substantial. RESULTS: Here we use a spatially-explicit computer simulation approach to investigate the human migration hypotheses of this region based on one-route or two-route models. We test the likelihood of each scenario by using Human Leukocyte Antigen (HLA) − A, −B, and − DRB1 genetic data of East Asian populations, with both selective and demographic parameters considered. The posterior distribution of each parameter is estimated by an Approximate Bayesian Computation (ABC) approach. CONCLUSIONS: Our results strongly support a model with two main routes of colonization of East Asia on both sides of the Himalayas, with distinct demographic histories in Northern and Southern populations, characterized by more isolation in the South. In East Asia, gene flow between populations originating from the two routes probably existed until a remote prehistoric period, explaining the continuous pattern of genetic variation currently observed along the latitude. A significant although dissimilar level of balancing selection acting on the three HLA loci is detected, but its effect on the local genetic patterns appears to be minor compared to those of past demographic events. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12862-015-0512-0) contains supplementary material, which is available to authorized users. BioMed Central 2015-11-04 /pmc/articles/PMC4632674/ /pubmed/26530905 http://dx.doi.org/10.1186/s12862-015-0512-0 Text en © Di et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Di, Da
Sanchez-Mazas, Alicia
Currat, Mathias
Computer simulation of human leukocyte antigen genes supports two main routes of colonization by human populations in East Asia
title Computer simulation of human leukocyte antigen genes supports two main routes of colonization by human populations in East Asia
title_full Computer simulation of human leukocyte antigen genes supports two main routes of colonization by human populations in East Asia
title_fullStr Computer simulation of human leukocyte antigen genes supports two main routes of colonization by human populations in East Asia
title_full_unstemmed Computer simulation of human leukocyte antigen genes supports two main routes of colonization by human populations in East Asia
title_short Computer simulation of human leukocyte antigen genes supports two main routes of colonization by human populations in East Asia
title_sort computer simulation of human leukocyte antigen genes supports two main routes of colonization by human populations in east asia
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4632674/
https://www.ncbi.nlm.nih.gov/pubmed/26530905
http://dx.doi.org/10.1186/s12862-015-0512-0
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