ArticleProceedings. Biological sciences2019
Release from intralocus sexual conflict? Evolved loss of a male sexual trait demasculinizes female gene expression.
Article in Proceedings. Biological sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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8 citing papers in PubMed.
- Does sexual dimorphism reflect sexual antagonism? Covariation of female fitness with brothers' sexual traits and their female homologues in neriid flies.Proceedings. Biological sciences · 2025Article
- Temporal genomics in Hawaiian crickets reveals compensatory intragenomic coadaptation during adaptive evolution.Nature communications · 2024Article
- A neglected conceptual problem regarding phenotypic plasticity's role in adaptive evolution: The importance of genetic covariance and social drive.Evolution letters · 2021Article
- Softness of selection and mating system interact to shape trait evolution under sexual conflict.Evolution; international journal of organic evolution · 2021Article
- Variable dosage compensation is associated with female consequences of an X-linked, male-beneficial mutation.Proceedings. Biological sciences · 2021Article
- Rapid parallel adaptation despite gene flow in silent crickets.Nature communications · 2021Article
- Field cricket genome reveals the footprint of recent, abrupt adaptation in the wild.Evolution letters · 2020Article
- Release from intralocus sexual conflict? Evolved loss of a male sexual trait demasculinizes female gene expression.Proceedings. Biological sciences · 2019Article
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3 authors.
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Abstract
The loss of sexual ornaments is observed across taxa, and pleiotropic effects of such losses provide an opportunity to gain insight into underlying dynamics of sex-biased gene expression and intralocus sexual conflict (IASC). We investigated this in a Hawaiian field cricket, Teleogryllus oceanicus, in which an X-linked genotype ( flatwing) feminizes males' wings and eliminates their ability to produce sexually selected songs. We profiled adult gene expression across somatic and reproductive tissues of both sexes. Despite the feminizing effect of flatwing on male wings, we found no evidence of feminized gene expression in males. Instead, female transcriptomes were more strongly affected by flatwing than males', and exhibited demasculinized gene expression. These findings are consistent with a relaxation of IASC constraining female gene expression through loss of a male sexual ornament. In a follow-up experiment, we found reduced testes mass in flatwing males, whereas female carriers showed no reduction in egg production. By contrast, female carriers exhibited greater measures of body condition. Our results suggest sex-limited phenotypic expression offers only partial resolution to IASC, owing to pleiotropic effects of the loci involved. Benefits conferred by release from intralocus conflict could help explain widespread loss of sexual ornaments across taxa.
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