Cargando…
Parallel genetic evolution and speciation from standing variation
Adaptation often proceeds from standing variation, and natural selection acting on pairs of populations is a quantitative continuum ranging from parallel to divergent. Yet, it is unclear how the extent of parallel genetic evolution during adaptation from standing variation is affected by the differe...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6591551/ https://www.ncbi.nlm.nih.gov/pubmed/31289688 http://dx.doi.org/10.1002/evl3.106 |
_version_ | 1783429754614972416 |
---|---|
author | Thompson, Ken A. Osmond, Matthew M. Schluter, Dolph |
author_facet | Thompson, Ken A. Osmond, Matthew M. Schluter, Dolph |
author_sort | Thompson, Ken A. |
collection | PubMed |
description | Adaptation often proceeds from standing variation, and natural selection acting on pairs of populations is a quantitative continuum ranging from parallel to divergent. Yet, it is unclear how the extent of parallel genetic evolution during adaptation from standing variation is affected by the difference in the direction of selection between populations. Nor is it clear whether the availability of standing variation for adaptation affects progress toward speciation in a manner that depends on the difference in the direction of selection. We conducted a theoretical study investigating these questions and have two primary findings. First, the extent of parallel genetic evolution between two populations rapidly declines as selection changes from fully parallel toward divergent, and this decline is steeper in organisms with more traits (i.e., greater dimensionality). This rapid decline happens because small differences in the direction of selection greatly reduce the fraction of alleles that are beneficial in both populations. For example, populations adapting to optima separated by an angle of 33° might have only 50% of potentially beneficial alleles in common. Second, relative to when adaptation is from only new mutation, adaptation from standing variation improves hybrid fitness under parallel selection and reduces hybrid fitness under divergent selection. Under parallel selection, genetic parallelism from standing variation reduces the phenotypic segregation variance in hybrids, thereby increasing mean fitness in the parental environment. Under divergent selection, larger pleiotropic effects of alleles fixed from standing variation cause maladaptive transgressive phenotypes when combined in hybrids. Adaptation from standing genetic variation therefore slows progress toward speciation under parallel selection and facilitates progress toward speciation under divergent selection. |
format | Online Article Text |
id | pubmed-6591551 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65915512019-07-09 Parallel genetic evolution and speciation from standing variation Thompson, Ken A. Osmond, Matthew M. Schluter, Dolph Evol Lett Letters Adaptation often proceeds from standing variation, and natural selection acting on pairs of populations is a quantitative continuum ranging from parallel to divergent. Yet, it is unclear how the extent of parallel genetic evolution during adaptation from standing variation is affected by the difference in the direction of selection between populations. Nor is it clear whether the availability of standing variation for adaptation affects progress toward speciation in a manner that depends on the difference in the direction of selection. We conducted a theoretical study investigating these questions and have two primary findings. First, the extent of parallel genetic evolution between two populations rapidly declines as selection changes from fully parallel toward divergent, and this decline is steeper in organisms with more traits (i.e., greater dimensionality). This rapid decline happens because small differences in the direction of selection greatly reduce the fraction of alleles that are beneficial in both populations. For example, populations adapting to optima separated by an angle of 33° might have only 50% of potentially beneficial alleles in common. Second, relative to when adaptation is from only new mutation, adaptation from standing variation improves hybrid fitness under parallel selection and reduces hybrid fitness under divergent selection. Under parallel selection, genetic parallelism from standing variation reduces the phenotypic segregation variance in hybrids, thereby increasing mean fitness in the parental environment. Under divergent selection, larger pleiotropic effects of alleles fixed from standing variation cause maladaptive transgressive phenotypes when combined in hybrids. Adaptation from standing genetic variation therefore slows progress toward speciation under parallel selection and facilitates progress toward speciation under divergent selection. John Wiley and Sons Inc. 2019-03-01 /pmc/articles/PMC6591551/ /pubmed/31289688 http://dx.doi.org/10.1002/evl3.106 Text en © 2019 The Author(s). Evolution Letters published by Wiley Periodicals, Inc. on behalf of Society for the Study of Evolution (SSE) and European Society for Evolutionary Biology (ESEB). This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Letters Thompson, Ken A. Osmond, Matthew M. Schluter, Dolph Parallel genetic evolution and speciation from standing variation |
title | Parallel genetic evolution and speciation from standing variation |
title_full | Parallel genetic evolution and speciation from standing variation |
title_fullStr | Parallel genetic evolution and speciation from standing variation |
title_full_unstemmed | Parallel genetic evolution and speciation from standing variation |
title_short | Parallel genetic evolution and speciation from standing variation |
title_sort | parallel genetic evolution and speciation from standing variation |
topic | Letters |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6591551/ https://www.ncbi.nlm.nih.gov/pubmed/31289688 http://dx.doi.org/10.1002/evl3.106 |
work_keys_str_mv | AT thompsonkena parallelgeneticevolutionandspeciationfromstandingvariation AT osmondmatthewm parallelgeneticevolutionandspeciationfromstandingvariation AT schluterdolph parallelgeneticevolutionandspeciationfromstandingvariation |