Cargando…
Experimental evidence of genome‐wide impact of ecological selection during early stages of speciation‐with‐gene‐flow
Theory predicts that speciation‐with‐gene‐flow is more likely when the consequences of selection for population divergence transitions from mainly direct effects of selection acting on individual genes to a collective property of all selected genes in the genome. Thus, understanding the direct impac...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4744793/ https://www.ncbi.nlm.nih.gov/pubmed/26077935 http://dx.doi.org/10.1111/ele.12460 |
_version_ | 1782414532229988352 |
---|---|
author | Egan, Scott P. Ragland, Gregory J. Assour, Lauren Powell, Thomas H.Q. Hood, Glen R. Emrich, Scott Nosil, Patrik Feder, Jeffrey L. |
author_facet | Egan, Scott P. Ragland, Gregory J. Assour, Lauren Powell, Thomas H.Q. Hood, Glen R. Emrich, Scott Nosil, Patrik Feder, Jeffrey L. |
author_sort | Egan, Scott P. |
collection | PubMed |
description | Theory predicts that speciation‐with‐gene‐flow is more likely when the consequences of selection for population divergence transitions from mainly direct effects of selection acting on individual genes to a collective property of all selected genes in the genome. Thus, understanding the direct impacts of ecologically based selection, as well as the indirect effects due to correlations among loci, is critical to understanding speciation. Here, we measure the genome‐wide impacts of host‐associated selection between hawthorn and apple host races of Rhagoletis pomonella (Diptera: Tephritidae), a model for contemporary speciation‐with‐gene‐flow. Allele frequency shifts of 32 455 SNPs induced in a selection experiment based on host phenology were genome wide and highly concordant with genetic divergence between co‐occurring apple and hawthorn flies in nature. This striking genome‐wide similarity between experimental and natural populations of R. pomonella underscores the importance of ecological selection at early stages of divergence and calls for further integration of studies of eco‐evolutionary dynamics and genome divergence. |
format | Online Article Text |
id | pubmed-4744793 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-47447932016-02-18 Experimental evidence of genome‐wide impact of ecological selection during early stages of speciation‐with‐gene‐flow Egan, Scott P. Ragland, Gregory J. Assour, Lauren Powell, Thomas H.Q. Hood, Glen R. Emrich, Scott Nosil, Patrik Feder, Jeffrey L. Ecol Lett Letters Theory predicts that speciation‐with‐gene‐flow is more likely when the consequences of selection for population divergence transitions from mainly direct effects of selection acting on individual genes to a collective property of all selected genes in the genome. Thus, understanding the direct impacts of ecologically based selection, as well as the indirect effects due to correlations among loci, is critical to understanding speciation. Here, we measure the genome‐wide impacts of host‐associated selection between hawthorn and apple host races of Rhagoletis pomonella (Diptera: Tephritidae), a model for contemporary speciation‐with‐gene‐flow. Allele frequency shifts of 32 455 SNPs induced in a selection experiment based on host phenology were genome wide and highly concordant with genetic divergence between co‐occurring apple and hawthorn flies in nature. This striking genome‐wide similarity between experimental and natural populations of R. pomonella underscores the importance of ecological selection at early stages of divergence and calls for further integration of studies of eco‐evolutionary dynamics and genome divergence. John Wiley and Sons Inc. 2015-06-15 2015-08 /pmc/articles/PMC4744793/ /pubmed/26077935 http://dx.doi.org/10.1111/ele.12460 Text en © 2015 The Authors Ecology Letters published by John Wiley & Sons Ltd and CNRS. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Letters Egan, Scott P. Ragland, Gregory J. Assour, Lauren Powell, Thomas H.Q. Hood, Glen R. Emrich, Scott Nosil, Patrik Feder, Jeffrey L. Experimental evidence of genome‐wide impact of ecological selection during early stages of speciation‐with‐gene‐flow |
title | Experimental evidence of genome‐wide impact of ecological selection during early stages of speciation‐with‐gene‐flow |
title_full | Experimental evidence of genome‐wide impact of ecological selection during early stages of speciation‐with‐gene‐flow |
title_fullStr | Experimental evidence of genome‐wide impact of ecological selection during early stages of speciation‐with‐gene‐flow |
title_full_unstemmed | Experimental evidence of genome‐wide impact of ecological selection during early stages of speciation‐with‐gene‐flow |
title_short | Experimental evidence of genome‐wide impact of ecological selection during early stages of speciation‐with‐gene‐flow |
title_sort | experimental evidence of genome‐wide impact of ecological selection during early stages of speciation‐with‐gene‐flow |
topic | Letters |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4744793/ https://www.ncbi.nlm.nih.gov/pubmed/26077935 http://dx.doi.org/10.1111/ele.12460 |
work_keys_str_mv | AT eganscottp experimentalevidenceofgenomewideimpactofecologicalselectionduringearlystagesofspeciationwithgeneflow AT raglandgregoryj experimentalevidenceofgenomewideimpactofecologicalselectionduringearlystagesofspeciationwithgeneflow AT assourlauren experimentalevidenceofgenomewideimpactofecologicalselectionduringearlystagesofspeciationwithgeneflow AT powellthomashq experimentalevidenceofgenomewideimpactofecologicalselectionduringearlystagesofspeciationwithgeneflow AT hoodglenr experimentalevidenceofgenomewideimpactofecologicalselectionduringearlystagesofspeciationwithgeneflow AT emrichscott experimentalevidenceofgenomewideimpactofecologicalselectionduringearlystagesofspeciationwithgeneflow AT nosilpatrik experimentalevidenceofgenomewideimpactofecologicalselectionduringearlystagesofspeciationwithgeneflow AT federjeffreyl experimentalevidenceofgenomewideimpactofecologicalselectionduringearlystagesofspeciationwithgeneflow |