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Male‐biased gene expression resolves sexual conflict through the evolution of sex‐specific genetic architecture

Many genes are subject to contradictory selection pressures in males and females, and balancing selection resulting from sexual conflict has the potential to substantially increase standing genetic diversity in populations and thereby act as an important force in adaptation. However, the underlying...

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Autores principales: Wright, Alison E., Fumagalli, Matteo, Cooney, Christopher R., Bloch, Natasha I., Vieira, Filipe G., Buechel, Severine D., Kolm, Niclas, Mank, Judith E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6089503/
https://www.ncbi.nlm.nih.gov/pubmed/30283664
http://dx.doi.org/10.1002/evl3.39
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author Wright, Alison E.
Fumagalli, Matteo
Cooney, Christopher R.
Bloch, Natasha I.
Vieira, Filipe G.
Buechel, Severine D.
Kolm, Niclas
Mank, Judith E.
author_facet Wright, Alison E.
Fumagalli, Matteo
Cooney, Christopher R.
Bloch, Natasha I.
Vieira, Filipe G.
Buechel, Severine D.
Kolm, Niclas
Mank, Judith E.
author_sort Wright, Alison E.
collection PubMed
description Many genes are subject to contradictory selection pressures in males and females, and balancing selection resulting from sexual conflict has the potential to substantially increase standing genetic diversity in populations and thereby act as an important force in adaptation. However, the underlying causes of sexual conflict, and the potential for resolution, remains hotly debated. Using transcriptome‐resequencing data from male and female guppies, we use a novel approach, combining patterns of genetic diversity and intersexual divergence in allele frequency, to distinguish the different scenarios that give rise to sexual conflict, and how this conflict may be resolved through regulatory evolution. We show that reproductive fitness is the main source of sexual conflict, and this is resolved via the evolution of male‐biased expression. Furthermore, resolution of sexual conflict produces significant differences in genetic architecture between males and females, which in turn lead to specific alleles influencing sex‐specific viability. Together, our findings suggest an important role for sexual conflict in shaping broad patterns of genome diversity, and show that regulatory evolution is a rapid and efficient route to the resolution of conflict.
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spelling pubmed-60895032018-10-03 Male‐biased gene expression resolves sexual conflict through the evolution of sex‐specific genetic architecture Wright, Alison E. Fumagalli, Matteo Cooney, Christopher R. Bloch, Natasha I. Vieira, Filipe G. Buechel, Severine D. Kolm, Niclas Mank, Judith E. Evol Lett Letters Many genes are subject to contradictory selection pressures in males and females, and balancing selection resulting from sexual conflict has the potential to substantially increase standing genetic diversity in populations and thereby act as an important force in adaptation. However, the underlying causes of sexual conflict, and the potential for resolution, remains hotly debated. Using transcriptome‐resequencing data from male and female guppies, we use a novel approach, combining patterns of genetic diversity and intersexual divergence in allele frequency, to distinguish the different scenarios that give rise to sexual conflict, and how this conflict may be resolved through regulatory evolution. We show that reproductive fitness is the main source of sexual conflict, and this is resolved via the evolution of male‐biased expression. Furthermore, resolution of sexual conflict produces significant differences in genetic architecture between males and females, which in turn lead to specific alleles influencing sex‐specific viability. Together, our findings suggest an important role for sexual conflict in shaping broad patterns of genome diversity, and show that regulatory evolution is a rapid and efficient route to the resolution of conflict. John Wiley and Sons Inc. 2018-02-10 /pmc/articles/PMC6089503/ /pubmed/30283664 http://dx.doi.org/10.1002/evl3.39 Text en © 2018 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
Wright, Alison E.
Fumagalli, Matteo
Cooney, Christopher R.
Bloch, Natasha I.
Vieira, Filipe G.
Buechel, Severine D.
Kolm, Niclas
Mank, Judith E.
Male‐biased gene expression resolves sexual conflict through the evolution of sex‐specific genetic architecture
title Male‐biased gene expression resolves sexual conflict through the evolution of sex‐specific genetic architecture
title_full Male‐biased gene expression resolves sexual conflict through the evolution of sex‐specific genetic architecture
title_fullStr Male‐biased gene expression resolves sexual conflict through the evolution of sex‐specific genetic architecture
title_full_unstemmed Male‐biased gene expression resolves sexual conflict through the evolution of sex‐specific genetic architecture
title_short Male‐biased gene expression resolves sexual conflict through the evolution of sex‐specific genetic architecture
title_sort male‐biased gene expression resolves sexual conflict through the evolution of sex‐specific genetic architecture
topic Letters
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6089503/
https://www.ncbi.nlm.nih.gov/pubmed/30283664
http://dx.doi.org/10.1002/evl3.39
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