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Repeated evolution of self-compatibility for reproductive assurance

Sexual reproduction in eukaryotes requires the fusion of two compatible gametes of opposite sexes or mating types. To meet the challenge of finding a mating partner with compatible gametes, evolutionary mechanisms such as hermaphroditism and self-fertilization have repeatedly evolved. Here, by combi...

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Autores principales: Nieuwenhuis, Bart P. S., Tusso, Sergio, Bjerling, Pernilla, Stångberg, Josefine, Wolf, Jochen B. W., Immler, Simone
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5915400/
https://www.ncbi.nlm.nih.gov/pubmed/29691402
http://dx.doi.org/10.1038/s41467-018-04054-6
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author Nieuwenhuis, Bart P. S.
Tusso, Sergio
Bjerling, Pernilla
Stångberg, Josefine
Wolf, Jochen B. W.
Immler, Simone
author_facet Nieuwenhuis, Bart P. S.
Tusso, Sergio
Bjerling, Pernilla
Stångberg, Josefine
Wolf, Jochen B. W.
Immler, Simone
author_sort Nieuwenhuis, Bart P. S.
collection PubMed
description Sexual reproduction in eukaryotes requires the fusion of two compatible gametes of opposite sexes or mating types. To meet the challenge of finding a mating partner with compatible gametes, evolutionary mechanisms such as hermaphroditism and self-fertilization have repeatedly evolved. Here, by combining the insights from comparative genomics, computer simulations and experimental evolution in fission yeast, we shed light on the conditions promoting separate mating types or self-compatibility by mating-type switching. Analogous to multiple independent transitions between switchers and non-switchers in natural populations mediated by structural genomic changes, novel switching genotypes readily evolved under selection in the experimental populations. Detailed fitness measurements accompanied by computer simulations show the benefits and costs of switching during sexual and asexual reproduction, governing the occurrence of both strategies in nature. Our findings illuminate the trade-off between the benefits of reproductive assurance and its fitness costs under benign conditions facilitating the evolution of self-compatibility.
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spelling pubmed-59154002018-04-27 Repeated evolution of self-compatibility for reproductive assurance Nieuwenhuis, Bart P. S. Tusso, Sergio Bjerling, Pernilla Stångberg, Josefine Wolf, Jochen B. W. Immler, Simone Nat Commun Article Sexual reproduction in eukaryotes requires the fusion of two compatible gametes of opposite sexes or mating types. To meet the challenge of finding a mating partner with compatible gametes, evolutionary mechanisms such as hermaphroditism and self-fertilization have repeatedly evolved. Here, by combining the insights from comparative genomics, computer simulations and experimental evolution in fission yeast, we shed light on the conditions promoting separate mating types or self-compatibility by mating-type switching. Analogous to multiple independent transitions between switchers and non-switchers in natural populations mediated by structural genomic changes, novel switching genotypes readily evolved under selection in the experimental populations. Detailed fitness measurements accompanied by computer simulations show the benefits and costs of switching during sexual and asexual reproduction, governing the occurrence of both strategies in nature. Our findings illuminate the trade-off between the benefits of reproductive assurance and its fitness costs under benign conditions facilitating the evolution of self-compatibility. Nature Publishing Group UK 2018-04-24 /pmc/articles/PMC5915400/ /pubmed/29691402 http://dx.doi.org/10.1038/s41467-018-04054-6 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Nieuwenhuis, Bart P. S.
Tusso, Sergio
Bjerling, Pernilla
Stångberg, Josefine
Wolf, Jochen B. W.
Immler, Simone
Repeated evolution of self-compatibility for reproductive assurance
title Repeated evolution of self-compatibility for reproductive assurance
title_full Repeated evolution of self-compatibility for reproductive assurance
title_fullStr Repeated evolution of self-compatibility for reproductive assurance
title_full_unstemmed Repeated evolution of self-compatibility for reproductive assurance
title_short Repeated evolution of self-compatibility for reproductive assurance
title_sort repeated evolution of self-compatibility for reproductive assurance
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5915400/
https://www.ncbi.nlm.nih.gov/pubmed/29691402
http://dx.doi.org/10.1038/s41467-018-04054-6
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