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Genetic dissection of assortative mating behavior
The evolution of new species is made easier when traits under divergent ecological selection are also mating cues. Such ecological mating cues are now considered more common than previously thought, but we still know little about the genetic changes underlying their evolution or more generally about...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6366751/ https://www.ncbi.nlm.nih.gov/pubmed/30730873 http://dx.doi.org/10.1371/journal.pbio.2005902 |
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author | Merrill, Richard M. Rastas, Pasi Martin, Simon H. Melo, Maria C. Barker, Sarah Davey, John McMillan, W. Owen Jiggins, Chris D. |
author_facet | Merrill, Richard M. Rastas, Pasi Martin, Simon H. Melo, Maria C. Barker, Sarah Davey, John McMillan, W. Owen Jiggins, Chris D. |
author_sort | Merrill, Richard M. |
collection | PubMed |
description | The evolution of new species is made easier when traits under divergent ecological selection are also mating cues. Such ecological mating cues are now considered more common than previously thought, but we still know little about the genetic changes underlying their evolution or more generally about the genetic basis for assortative mating behaviors. Both tight physical linkage and the existence of large-effect preference loci will strengthen genetic associations between behavioral and ecological barriers, promoting the evolution of assortative mating. The warning patterns of Heliconius melpomene and H. cydno are under disruptive selection due to increased predation of nonmimetic hybrids and are used during mate recognition. We carried out a genome-wide quantitative trait locus (QTL) analysis of preference behaviors between these species and showed that divergent male preference has a simple genetic basis. We identify three QTLs that together explain a large proportion (approximately 60%) of the difference in preference behavior observed between the parental species. One of these QTLs is just 1.2 (0–4.8) centiMorgans (cM) from the major color pattern gene optix, and, individually, all three have a large effect on the preference phenotype. Genomic divergence between H. cydno and H. melpomene is high but broadly heterogenous, and admixture is reduced at the preference–optix color pattern locus but not the other preference QTLs. The simple genetic architecture we reveal will facilitate the evolution and maintenance of new species despite ongoing gene flow by coupling behavioral and ecological aspects of reproductive isolation. |
format | Online Article Text |
id | pubmed-6366751 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-63667512019-02-22 Genetic dissection of assortative mating behavior Merrill, Richard M. Rastas, Pasi Martin, Simon H. Melo, Maria C. Barker, Sarah Davey, John McMillan, W. Owen Jiggins, Chris D. PLoS Biol Research Article The evolution of new species is made easier when traits under divergent ecological selection are also mating cues. Such ecological mating cues are now considered more common than previously thought, but we still know little about the genetic changes underlying their evolution or more generally about the genetic basis for assortative mating behaviors. Both tight physical linkage and the existence of large-effect preference loci will strengthen genetic associations between behavioral and ecological barriers, promoting the evolution of assortative mating. The warning patterns of Heliconius melpomene and H. cydno are under disruptive selection due to increased predation of nonmimetic hybrids and are used during mate recognition. We carried out a genome-wide quantitative trait locus (QTL) analysis of preference behaviors between these species and showed that divergent male preference has a simple genetic basis. We identify three QTLs that together explain a large proportion (approximately 60%) of the difference in preference behavior observed between the parental species. One of these QTLs is just 1.2 (0–4.8) centiMorgans (cM) from the major color pattern gene optix, and, individually, all three have a large effect on the preference phenotype. Genomic divergence between H. cydno and H. melpomene is high but broadly heterogenous, and admixture is reduced at the preference–optix color pattern locus but not the other preference QTLs. The simple genetic architecture we reveal will facilitate the evolution and maintenance of new species despite ongoing gene flow by coupling behavioral and ecological aspects of reproductive isolation. Public Library of Science 2019-02-07 /pmc/articles/PMC6366751/ /pubmed/30730873 http://dx.doi.org/10.1371/journal.pbio.2005902 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication. |
spellingShingle | Research Article Merrill, Richard M. Rastas, Pasi Martin, Simon H. Melo, Maria C. Barker, Sarah Davey, John McMillan, W. Owen Jiggins, Chris D. Genetic dissection of assortative mating behavior |
title | Genetic dissection of assortative mating behavior |
title_full | Genetic dissection of assortative mating behavior |
title_fullStr | Genetic dissection of assortative mating behavior |
title_full_unstemmed | Genetic dissection of assortative mating behavior |
title_short | Genetic dissection of assortative mating behavior |
title_sort | genetic dissection of assortative mating behavior |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6366751/ https://www.ncbi.nlm.nih.gov/pubmed/30730873 http://dx.doi.org/10.1371/journal.pbio.2005902 |
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