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A Genomic Map of the Effects of Linked Selection in Drosophila

Natural selection at one site shapes patterns of genetic variation at linked sites. Quantifying the effects of “linked selection” on levels of genetic diversity is key to making reliable inference about demography, building a null model in scans for targets of adaptation, and learning about the dyna...

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Autores principales: Elyashiv, Eyal, Sattath, Shmuel, Hu, Tina T., Strutsovsky, Alon, McVicker, Graham, Andolfatto, Peter, Coop, Graham, Sella, Guy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4990265/
https://www.ncbi.nlm.nih.gov/pubmed/27536991
http://dx.doi.org/10.1371/journal.pgen.1006130
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author Elyashiv, Eyal
Sattath, Shmuel
Hu, Tina T.
Strutsovsky, Alon
McVicker, Graham
Andolfatto, Peter
Coop, Graham
Sella, Guy
author_facet Elyashiv, Eyal
Sattath, Shmuel
Hu, Tina T.
Strutsovsky, Alon
McVicker, Graham
Andolfatto, Peter
Coop, Graham
Sella, Guy
author_sort Elyashiv, Eyal
collection PubMed
description Natural selection at one site shapes patterns of genetic variation at linked sites. Quantifying the effects of “linked selection” on levels of genetic diversity is key to making reliable inference about demography, building a null model in scans for targets of adaptation, and learning about the dynamics of natural selection. Here, we introduce the first method that jointly infers parameters of distinct modes of linked selection, notably background selection and selective sweeps, from genome-wide diversity data, functional annotations and genetic maps. The central idea is to calculate the probability that a neutral site is polymorphic given local annotations, substitution patterns, and recombination rates. Information is then combined across sites and samples using composite likelihood in order to estimate genome-wide parameters of distinct modes of selection. In addition to parameter estimation, this approach yields a map of the expected neutral diversity levels along the genome. To illustrate the utility of our approach, we apply it to genome-wide resequencing data from 125 lines in Drosophila melanogaster and reliably predict diversity levels at the 1Mb scale. Our results corroborate estimates of a high fraction of beneficial substitutions in proteins and untranslated regions (UTR). They allow us to distinguish between the contribution of sweeps and other modes of selection around amino acid substitutions and to uncover evidence for pervasive sweeps in untranslated regions (UTRs). Our inference further suggests a substantial effect of other modes of linked selection and of adaptation in particular. More generally, we demonstrate that linked selection has had a larger effect in reducing diversity levels and increasing their variance in D. melanogaster than previously appreciated.
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spelling pubmed-49902652016-08-29 A Genomic Map of the Effects of Linked Selection in Drosophila Elyashiv, Eyal Sattath, Shmuel Hu, Tina T. Strutsovsky, Alon McVicker, Graham Andolfatto, Peter Coop, Graham Sella, Guy PLoS Genet Research Article Natural selection at one site shapes patterns of genetic variation at linked sites. Quantifying the effects of “linked selection” on levels of genetic diversity is key to making reliable inference about demography, building a null model in scans for targets of adaptation, and learning about the dynamics of natural selection. Here, we introduce the first method that jointly infers parameters of distinct modes of linked selection, notably background selection and selective sweeps, from genome-wide diversity data, functional annotations and genetic maps. The central idea is to calculate the probability that a neutral site is polymorphic given local annotations, substitution patterns, and recombination rates. Information is then combined across sites and samples using composite likelihood in order to estimate genome-wide parameters of distinct modes of selection. In addition to parameter estimation, this approach yields a map of the expected neutral diversity levels along the genome. To illustrate the utility of our approach, we apply it to genome-wide resequencing data from 125 lines in Drosophila melanogaster and reliably predict diversity levels at the 1Mb scale. Our results corroborate estimates of a high fraction of beneficial substitutions in proteins and untranslated regions (UTR). They allow us to distinguish between the contribution of sweeps and other modes of selection around amino acid substitutions and to uncover evidence for pervasive sweeps in untranslated regions (UTRs). Our inference further suggests a substantial effect of other modes of linked selection and of adaptation in particular. More generally, we demonstrate that linked selection has had a larger effect in reducing diversity levels and increasing their variance in D. melanogaster than previously appreciated. Public Library of Science 2016-08-18 /pmc/articles/PMC4990265/ /pubmed/27536991 http://dx.doi.org/10.1371/journal.pgen.1006130 Text en © 2016 Elyashiv 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Elyashiv, Eyal
Sattath, Shmuel
Hu, Tina T.
Strutsovsky, Alon
McVicker, Graham
Andolfatto, Peter
Coop, Graham
Sella, Guy
A Genomic Map of the Effects of Linked Selection in Drosophila
title A Genomic Map of the Effects of Linked Selection in Drosophila
title_full A Genomic Map of the Effects of Linked Selection in Drosophila
title_fullStr A Genomic Map of the Effects of Linked Selection in Drosophila
title_full_unstemmed A Genomic Map of the Effects of Linked Selection in Drosophila
title_short A Genomic Map of the Effects of Linked Selection in Drosophila
title_sort genomic map of the effects of linked selection in drosophila
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4990265/
https://www.ncbi.nlm.nih.gov/pubmed/27536991
http://dx.doi.org/10.1371/journal.pgen.1006130
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