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The evolution of hybrid fitness during speciation
The evolution of postzygotic reproductive isolation is an important component of speciation. But before isolation is complete there is sometimes a phase of heterosis in which hybrid fitness exceeds that of the two parental species. The genetics and evolution of heterosis and postzygotic isolation ha...
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/PMC6502311/ https://www.ncbi.nlm.nih.gov/pubmed/31059513 http://dx.doi.org/10.1371/journal.pgen.1008125 |
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author | Dagilis, Andrius J. Kirkpatrick, Mark Bolnick, Daniel I. |
author_facet | Dagilis, Andrius J. Kirkpatrick, Mark Bolnick, Daniel I. |
author_sort | Dagilis, Andrius J. |
collection | PubMed |
description | The evolution of postzygotic reproductive isolation is an important component of speciation. But before isolation is complete there is sometimes a phase of heterosis in which hybrid fitness exceeds that of the two parental species. The genetics and evolution of heterosis and postzygotic isolation have typically been studied in isolation, precluding the development of a unified theory of speciation. Here, we develop a model that incorporates both positive and negative gene interactions, and accounts for the evolution of both heterosis and postzygotic isolation. We parameterize the model with recent data on the fitness effects of 10,000 mutations in yeast, singly and in pairwise epistatic combinations. The model makes novel predictions about the types of interactions that contribute to declining hybrid fitness. We reproduce patterns familiar from earlier models of speciation (e.g. Haldane’s Rule and Darwin’s Corollary) and identify new mechanisms that may underlie these patterns. Our approach provides a general framework for integrating experimental data from gene interaction networks into speciation theory and makes new predictions about the genetic mechanisms of speciation. |
format | Online Article Text |
id | pubmed-6502311 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-65023112019-05-23 The evolution of hybrid fitness during speciation Dagilis, Andrius J. Kirkpatrick, Mark Bolnick, Daniel I. PLoS Genet Research Article The evolution of postzygotic reproductive isolation is an important component of speciation. But before isolation is complete there is sometimes a phase of heterosis in which hybrid fitness exceeds that of the two parental species. The genetics and evolution of heterosis and postzygotic isolation have typically been studied in isolation, precluding the development of a unified theory of speciation. Here, we develop a model that incorporates both positive and negative gene interactions, and accounts for the evolution of both heterosis and postzygotic isolation. We parameterize the model with recent data on the fitness effects of 10,000 mutations in yeast, singly and in pairwise epistatic combinations. The model makes novel predictions about the types of interactions that contribute to declining hybrid fitness. We reproduce patterns familiar from earlier models of speciation (e.g. Haldane’s Rule and Darwin’s Corollary) and identify new mechanisms that may underlie these patterns. Our approach provides a general framework for integrating experimental data from gene interaction networks into speciation theory and makes new predictions about the genetic mechanisms of speciation. Public Library of Science 2019-05-06 /pmc/articles/PMC6502311/ /pubmed/31059513 http://dx.doi.org/10.1371/journal.pgen.1008125 Text en © 2019 Dagilis 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 Dagilis, Andrius J. Kirkpatrick, Mark Bolnick, Daniel I. The evolution of hybrid fitness during speciation |
title | The evolution of hybrid fitness during speciation |
title_full | The evolution of hybrid fitness during speciation |
title_fullStr | The evolution of hybrid fitness during speciation |
title_full_unstemmed | The evolution of hybrid fitness during speciation |
title_short | The evolution of hybrid fitness during speciation |
title_sort | evolution of hybrid fitness during speciation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6502311/ https://www.ncbi.nlm.nih.gov/pubmed/31059513 http://dx.doi.org/10.1371/journal.pgen.1008125 |
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