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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...

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Detalles Bibliográficos
Autores principales: Dagilis, Andrius J., Kirkpatrick, Mark, Bolnick, Daniel I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
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.
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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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