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Intrinsic emergence and modulation of sex‐specific dominance reversals in threshold traits
Sex‐specific dominance reversals (SSDRs) in fitness‐related traits, where heterozygotes' phenotypes resemble those of alternative homozygotes in females versus males, can simultaneously maintain genetic variation in fitness and resolve sexual conflict and thereby shape key evolutionary outcomes...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9541474/ https://www.ncbi.nlm.nih.gov/pubmed/35803581 http://dx.doi.org/10.1111/evo.14563 |
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author | Reid, Jane M. |
author_facet | Reid, Jane M. |
author_sort | Reid, Jane M. |
collection | PubMed |
description | Sex‐specific dominance reversals (SSDRs) in fitness‐related traits, where heterozygotes' phenotypes resemble those of alternative homozygotes in females versus males, can simultaneously maintain genetic variation in fitness and resolve sexual conflict and thereby shape key evolutionary outcomes. However, the full implications of SSDRs will depend on how they arise and the resulting potential for evolutionary, ecological and environmental modulation. Recent field and laboratory studies have demonstrated SSDRs in threshold(‐like) traits with dichotomous or competitive phenotypic outcomes, implying that such traits could promote the emergence of SSDRs. However, such possibilities have not been explicitly examined. I show how phenotypic SSDRs can readily emerge in threshold traits given genetic architectures involving large‐effect loci alongside sexual dimorphism in the mean and variance in polygenic liability. I also show how multilocus SSDRs can arise in line‐cross experiments, especially given competitive reproductive systems that generate nonlinear fitness outcomes. SSDRs can consequently emerge in threshold(‐like) traits as functions of sexual antagonism, sexual dimorphism and reproductive systems, even with purely additive underlying genetic effects. Accordingly, I identify theoretical and empirical advances that are now required to discern the basis and occurrence of SSDRs in nature, probe forms of (co‐)evolutionary, ecological and environmental modulation, and evaluate net impacts on sexual conflict. |
format | Online Article Text |
id | pubmed-9541474 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95414742022-10-14 Intrinsic emergence and modulation of sex‐specific dominance reversals in threshold traits Reid, Jane M. Evolution Perspective Sex‐specific dominance reversals (SSDRs) in fitness‐related traits, where heterozygotes' phenotypes resemble those of alternative homozygotes in females versus males, can simultaneously maintain genetic variation in fitness and resolve sexual conflict and thereby shape key evolutionary outcomes. However, the full implications of SSDRs will depend on how they arise and the resulting potential for evolutionary, ecological and environmental modulation. Recent field and laboratory studies have demonstrated SSDRs in threshold(‐like) traits with dichotomous or competitive phenotypic outcomes, implying that such traits could promote the emergence of SSDRs. However, such possibilities have not been explicitly examined. I show how phenotypic SSDRs can readily emerge in threshold traits given genetic architectures involving large‐effect loci alongside sexual dimorphism in the mean and variance in polygenic liability. I also show how multilocus SSDRs can arise in line‐cross experiments, especially given competitive reproductive systems that generate nonlinear fitness outcomes. SSDRs can consequently emerge in threshold(‐like) traits as functions of sexual antagonism, sexual dimorphism and reproductive systems, even with purely additive underlying genetic effects. Accordingly, I identify theoretical and empirical advances that are now required to discern the basis and occurrence of SSDRs in nature, probe forms of (co‐)evolutionary, ecological and environmental modulation, and evaluate net impacts on sexual conflict. John Wiley and Sons Inc. 2022-07-20 2022-09 /pmc/articles/PMC9541474/ /pubmed/35803581 http://dx.doi.org/10.1111/evo.14563 Text en © 2022 The Authors. Evolution published by Wiley Periodicals LLC on behalf of The Society for the Study of Evolution. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Perspective Reid, Jane M. Intrinsic emergence and modulation of sex‐specific dominance reversals in threshold traits |
title | Intrinsic emergence and modulation of sex‐specific dominance reversals in threshold traits |
title_full | Intrinsic emergence and modulation of sex‐specific dominance reversals in threshold traits |
title_fullStr | Intrinsic emergence and modulation of sex‐specific dominance reversals in threshold traits |
title_full_unstemmed | Intrinsic emergence and modulation of sex‐specific dominance reversals in threshold traits |
title_short | Intrinsic emergence and modulation of sex‐specific dominance reversals in threshold traits |
title_sort | intrinsic emergence and modulation of sex‐specific dominance reversals in threshold traits |
topic | Perspective |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9541474/ https://www.ncbi.nlm.nih.gov/pubmed/35803581 http://dx.doi.org/10.1111/evo.14563 |
work_keys_str_mv | AT reidjanem intrinsicemergenceandmodulationofsexspecificdominancereversalsinthresholdtraits |