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Sexually antagonistic selection during parental care is not generated by a testosterone-related intralocus sexual conflict–insights from full-sib comparisons

The evolution of shared male and female traits can be hampered if selection favours sex-specific optima. However, such genomic conflicts can be resolved when independent male and female mechanisms evolve. The existence, extent and consequences of conflict and/or conflict resolution are currently deb...

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Autores principales: Iserbyt, Arne, Eens, Marcel, Müller, Wendt
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4667218/
https://www.ncbi.nlm.nih.gov/pubmed/26625951
http://dx.doi.org/10.1038/srep17715
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author Iserbyt, Arne
Eens, Marcel
Müller, Wendt
author_facet Iserbyt, Arne
Eens, Marcel
Müller, Wendt
author_sort Iserbyt, Arne
collection PubMed
description The evolution of shared male and female traits can be hampered if selection favours sex-specific optima. However, such genomic conflicts can be resolved when independent male and female mechanisms evolve. The existence, extent and consequences of conflict and/or conflict resolution are currently debated. Endocrinological traits like plasma testosterone (T) are suitable test cases, given their important role in mediating correlated traits, plus their opposing sex-specific fitness effects. We compared full-sibling (brother/sister) captive canaries to test for (1) sexually antagonistic selection characterized by contrasting fitness patterns within pairs of relatives, (2) intersexual genetic correlation of plasma T (h(²) = 0.41  ±  0.31) and (3) intralocus sexual conflict over T levels featured by distinct sex-specific fitness optima. We found potential for sexually antagonistic selection, since high fledgling mass was reached by either brothers or sisters, but not by both. We report a positive intersexual correlation for T, as a requirement for intralocus sexual conflict. However, high levels of T were associated with increased female and decreased male fitness (fledgling mass), which contrasts our expectations and challenges the hypothesis of intralocus sexual conflict driven by T. We hypothesize that behavioural and physiological trade-offs differ between sexes when raising offspring, driving T levels towards a state of monomorphism.
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spelling pubmed-46672182015-12-08 Sexually antagonistic selection during parental care is not generated by a testosterone-related intralocus sexual conflict–insights from full-sib comparisons Iserbyt, Arne Eens, Marcel Müller, Wendt Sci Rep Article The evolution of shared male and female traits can be hampered if selection favours sex-specific optima. However, such genomic conflicts can be resolved when independent male and female mechanisms evolve. The existence, extent and consequences of conflict and/or conflict resolution are currently debated. Endocrinological traits like plasma testosterone (T) are suitable test cases, given their important role in mediating correlated traits, plus their opposing sex-specific fitness effects. We compared full-sibling (brother/sister) captive canaries to test for (1) sexually antagonistic selection characterized by contrasting fitness patterns within pairs of relatives, (2) intersexual genetic correlation of plasma T (h(²) = 0.41  ±  0.31) and (3) intralocus sexual conflict over T levels featured by distinct sex-specific fitness optima. We found potential for sexually antagonistic selection, since high fledgling mass was reached by either brothers or sisters, but not by both. We report a positive intersexual correlation for T, as a requirement for intralocus sexual conflict. However, high levels of T were associated with increased female and decreased male fitness (fledgling mass), which contrasts our expectations and challenges the hypothesis of intralocus sexual conflict driven by T. We hypothesize that behavioural and physiological trade-offs differ between sexes when raising offspring, driving T levels towards a state of monomorphism. Nature Publishing Group 2015-12-02 /pmc/articles/PMC4667218/ /pubmed/26625951 http://dx.doi.org/10.1038/srep17715 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Iserbyt, Arne
Eens, Marcel
Müller, Wendt
Sexually antagonistic selection during parental care is not generated by a testosterone-related intralocus sexual conflict–insights from full-sib comparisons
title Sexually antagonistic selection during parental care is not generated by a testosterone-related intralocus sexual conflict–insights from full-sib comparisons
title_full Sexually antagonistic selection during parental care is not generated by a testosterone-related intralocus sexual conflict–insights from full-sib comparisons
title_fullStr Sexually antagonistic selection during parental care is not generated by a testosterone-related intralocus sexual conflict–insights from full-sib comparisons
title_full_unstemmed Sexually antagonistic selection during parental care is not generated by a testosterone-related intralocus sexual conflict–insights from full-sib comparisons
title_short Sexually antagonistic selection during parental care is not generated by a testosterone-related intralocus sexual conflict–insights from full-sib comparisons
title_sort sexually antagonistic selection during parental care is not generated by a testosterone-related intralocus sexual conflict–insights from full-sib comparisons
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4667218/
https://www.ncbi.nlm.nih.gov/pubmed/26625951
http://dx.doi.org/10.1038/srep17715
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