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Human genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequences

BACKGROUND: Population differentiation has proved to be effective for identifying loci under geographically localized positive selection, and has the potential to identify loci subject to balancing selection. We have previously investigated the pattern of genetic differentiation among human populati...

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Autores principales: Colonna, Vincenza, Ayub, Qasim, Chen, Yuan, Pagani, Luca, Luisi, Pierre, Pybus, Marc, Garrison, Erik, Xue, Yali, Tyler-Smith, Chris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4197830/
https://www.ncbi.nlm.nih.gov/pubmed/24980144
http://dx.doi.org/10.1186/gb-2014-15-6-r88
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author Colonna, Vincenza
Ayub, Qasim
Chen, Yuan
Pagani, Luca
Luisi, Pierre
Pybus, Marc
Garrison, Erik
Xue, Yali
Tyler-Smith, Chris
author_facet Colonna, Vincenza
Ayub, Qasim
Chen, Yuan
Pagani, Luca
Luisi, Pierre
Pybus, Marc
Garrison, Erik
Xue, Yali
Tyler-Smith, Chris
author_sort Colonna, Vincenza
collection PubMed
description BACKGROUND: Population differentiation has proved to be effective for identifying loci under geographically localized positive selection, and has the potential to identify loci subject to balancing selection. We have previously investigated the pattern of genetic differentiation among human populations at 36.8 million genomic variants to identify sites in the genome showing high frequency differences. Here, we extend this dataset to include additional variants, survey sites with low levels of differentiation, and evaluate the extent to which highly differentiated sites are likely to result from selective or other processes. RESULTS: We demonstrate that while sites with low differentiation represent sampling effects rather than balancing selection, sites showing extremely high population differentiation are enriched for positive selection events and that one half may be the result of classic selective sweeps. Among these, we rediscover known examples, where we actually identify the established functional SNP, and discover novel examples including the genes ABCA12, CALD1 and ZNF804, which we speculate may be linked to adaptations in skin, calcium metabolism and defense, respectively. CONCLUSIONS: We identify known and many novel candidate regions for geographically restricted positive selection, and suggest several directions for further research.
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spelling pubmed-41978302014-10-16 Human genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequences Colonna, Vincenza Ayub, Qasim Chen, Yuan Pagani, Luca Luisi, Pierre Pybus, Marc Garrison, Erik Xue, Yali Tyler-Smith, Chris Genome Biol Research BACKGROUND: Population differentiation has proved to be effective for identifying loci under geographically localized positive selection, and has the potential to identify loci subject to balancing selection. We have previously investigated the pattern of genetic differentiation among human populations at 36.8 million genomic variants to identify sites in the genome showing high frequency differences. Here, we extend this dataset to include additional variants, survey sites with low levels of differentiation, and evaluate the extent to which highly differentiated sites are likely to result from selective or other processes. RESULTS: We demonstrate that while sites with low differentiation represent sampling effects rather than balancing selection, sites showing extremely high population differentiation are enriched for positive selection events and that one half may be the result of classic selective sweeps. Among these, we rediscover known examples, where we actually identify the established functional SNP, and discover novel examples including the genes ABCA12, CALD1 and ZNF804, which we speculate may be linked to adaptations in skin, calcium metabolism and defense, respectively. CONCLUSIONS: We identify known and many novel candidate regions for geographically restricted positive selection, and suggest several directions for further research. BioMed Central 2014 2014-06-30 /pmc/articles/PMC4197830/ /pubmed/24980144 http://dx.doi.org/10.1186/gb-2014-15-6-r88 Text en Copyright © 2014 Colonna et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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
Colonna, Vincenza
Ayub, Qasim
Chen, Yuan
Pagani, Luca
Luisi, Pierre
Pybus, Marc
Garrison, Erik
Xue, Yali
Tyler-Smith, Chris
Human genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequences
title Human genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequences
title_full Human genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequences
title_fullStr Human genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequences
title_full_unstemmed Human genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequences
title_short Human genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequences
title_sort human genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequences
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4197830/
https://www.ncbi.nlm.nih.gov/pubmed/24980144
http://dx.doi.org/10.1186/gb-2014-15-6-r88
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