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A gene's-eye view of sexual antagonism

Females and males may face different selection pressures. Accordingly, alleles that confer a benefit for one sex often incur a cost for the other. Classic evolutionary theory holds that the X chromosome, whose sex-biased transmission sees it spending more time in females, should value females more t...

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Detalles Bibliográficos
Autores principales: Hitchcock, Thomas J., Gardner, Andy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7575522/
https://www.ncbi.nlm.nih.gov/pubmed/32781951
http://dx.doi.org/10.1098/rspb.2020.1633
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author Hitchcock, Thomas J.
Gardner, Andy
author_facet Hitchcock, Thomas J.
Gardner, Andy
author_sort Hitchcock, Thomas J.
collection PubMed
description Females and males may face different selection pressures. Accordingly, alleles that confer a benefit for one sex often incur a cost for the other. Classic evolutionary theory holds that the X chromosome, whose sex-biased transmission sees it spending more time in females, should value females more than males, whereas autosomes, whose transmission is unbiased, should value both sexes equally. However, recent mathematical and empirical studies indicate that male-beneficial alleles may be more favoured by the X chromosome than by autosomes. Here we develop a gene's-eye-view approach that reconciles the classic view with these recent discordant results, by separating a gene's valuation of female versus male fitness from its ability to induce fitness effects in either sex. We use this framework to generate new comparative predictions for sexually antagonistic evolution in relation to dosage compensation, sex-specific mortality and assortative mating, revealing how molecular mechanisms, ecology and demography drive variation in masculinization versus feminization across the genome.
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spelling pubmed-75755222020-10-21 A gene's-eye view of sexual antagonism Hitchcock, Thomas J. Gardner, Andy Proc Biol Sci Evolution Females and males may face different selection pressures. Accordingly, alleles that confer a benefit for one sex often incur a cost for the other. Classic evolutionary theory holds that the X chromosome, whose sex-biased transmission sees it spending more time in females, should value females more than males, whereas autosomes, whose transmission is unbiased, should value both sexes equally. However, recent mathematical and empirical studies indicate that male-beneficial alleles may be more favoured by the X chromosome than by autosomes. Here we develop a gene's-eye-view approach that reconciles the classic view with these recent discordant results, by separating a gene's valuation of female versus male fitness from its ability to induce fitness effects in either sex. We use this framework to generate new comparative predictions for sexually antagonistic evolution in relation to dosage compensation, sex-specific mortality and assortative mating, revealing how molecular mechanisms, ecology and demography drive variation in masculinization versus feminization across the genome. The Royal Society 2020-08-12 2020-08-12 /pmc/articles/PMC7575522/ /pubmed/32781951 http://dx.doi.org/10.1098/rspb.2020.1633 Text en © 2020 The Authors. http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/http://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Evolution
Hitchcock, Thomas J.
Gardner, Andy
A gene's-eye view of sexual antagonism
title A gene's-eye view of sexual antagonism
title_full A gene's-eye view of sexual antagonism
title_fullStr A gene's-eye view of sexual antagonism
title_full_unstemmed A gene's-eye view of sexual antagonism
title_short A gene's-eye view of sexual antagonism
title_sort gene's-eye view of sexual antagonism
topic Evolution
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7575522/
https://www.ncbi.nlm.nih.gov/pubmed/32781951
http://dx.doi.org/10.1098/rspb.2020.1633
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