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Reconstructing recent population history while mapping rare variants using haplotypes

Haplotype-based methods are a cost-effective alternative to characterize unobserved rare variants and map disease-associated alleles. Moreover, they can be used to reconstruct recent population history, which shaped distribution of rare variants and thus can be used to guide gene mapping studies. In...

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Autores principales: Yunusbaev, Ural, Valeev, Albert, Yunusbaeva, Milyausha, Kwon, Hyung Wook, Mägi, Reedik, Metspalu, Mait, Yunusbayev, Bayazit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6458133/
https://www.ncbi.nlm.nih.gov/pubmed/30971755
http://dx.doi.org/10.1038/s41598-019-42385-6
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author Yunusbaev, Ural
Valeev, Albert
Yunusbaeva, Milyausha
Kwon, Hyung Wook
Mägi, Reedik
Metspalu, Mait
Yunusbayev, Bayazit
author_facet Yunusbaev, Ural
Valeev, Albert
Yunusbaeva, Milyausha
Kwon, Hyung Wook
Mägi, Reedik
Metspalu, Mait
Yunusbayev, Bayazit
author_sort Yunusbaev, Ural
collection PubMed
description Haplotype-based methods are a cost-effective alternative to characterize unobserved rare variants and map disease-associated alleles. Moreover, they can be used to reconstruct recent population history, which shaped distribution of rare variants and thus can be used to guide gene mapping studies. In this study, we analysed Illumina 650 k genotyped dataset on three underrepresented populations from Eastern Europe, where ancestors of Russians came into contact with two indigenous ethnic groups, Bashkirs and Tatars. Using the IBD mapping approach, we identified two rare IBD haplotypes strongly enriched in asthma patients of distinct ethnic background. We reconstructed recent population history using haplotype-based methods to reconcile this contradictory finding. Our ChromoPainter analysis showed that these haplotypes each descend from a single ancestor coming from one of the ethnic groups studied. Next, we used DoRIS approach and showed that source populations for patients exchanged recent (<60 generations) asymmetric gene flow, which supported the ChromoPainter-based scenario that patients share haplotypes through inter-ethnic admixture. Finally, we show that these IBD haplotypes overlap with asthma-associated genomic regions ascertained in European population. This finding is consistent with the fact that the two donor populations for the rare IBD haplotypes: Russians and Tatars have European ancestry.
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spelling pubmed-64581332019-04-15 Reconstructing recent population history while mapping rare variants using haplotypes Yunusbaev, Ural Valeev, Albert Yunusbaeva, Milyausha Kwon, Hyung Wook Mägi, Reedik Metspalu, Mait Yunusbayev, Bayazit Sci Rep Article Haplotype-based methods are a cost-effective alternative to characterize unobserved rare variants and map disease-associated alleles. Moreover, they can be used to reconstruct recent population history, which shaped distribution of rare variants and thus can be used to guide gene mapping studies. In this study, we analysed Illumina 650 k genotyped dataset on three underrepresented populations from Eastern Europe, where ancestors of Russians came into contact with two indigenous ethnic groups, Bashkirs and Tatars. Using the IBD mapping approach, we identified two rare IBD haplotypes strongly enriched in asthma patients of distinct ethnic background. We reconstructed recent population history using haplotype-based methods to reconcile this contradictory finding. Our ChromoPainter analysis showed that these haplotypes each descend from a single ancestor coming from one of the ethnic groups studied. Next, we used DoRIS approach and showed that source populations for patients exchanged recent (<60 generations) asymmetric gene flow, which supported the ChromoPainter-based scenario that patients share haplotypes through inter-ethnic admixture. Finally, we show that these IBD haplotypes overlap with asthma-associated genomic regions ascertained in European population. This finding is consistent with the fact that the two donor populations for the rare IBD haplotypes: Russians and Tatars have European ancestry. Nature Publishing Group UK 2019-04-10 /pmc/articles/PMC6458133/ /pubmed/30971755 http://dx.doi.org/10.1038/s41598-019-42385-6 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Yunusbaev, Ural
Valeev, Albert
Yunusbaeva, Milyausha
Kwon, Hyung Wook
Mägi, Reedik
Metspalu, Mait
Yunusbayev, Bayazit
Reconstructing recent population history while mapping rare variants using haplotypes
title Reconstructing recent population history while mapping rare variants using haplotypes
title_full Reconstructing recent population history while mapping rare variants using haplotypes
title_fullStr Reconstructing recent population history while mapping rare variants using haplotypes
title_full_unstemmed Reconstructing recent population history while mapping rare variants using haplotypes
title_short Reconstructing recent population history while mapping rare variants using haplotypes
title_sort reconstructing recent population history while mapping rare variants using haplotypes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6458133/
https://www.ncbi.nlm.nih.gov/pubmed/30971755
http://dx.doi.org/10.1038/s41598-019-42385-6
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