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Mating Changes Sexually Dimorphic Gene Expression in the Seed Beetle Callosobruchus maculatus

Sexually dimorphic phenotypes arise largely from sex-specific gene expression, which has mainly been characterized in sexually naïve adults. However, we expect sexual dimorphism in transcription to be dynamic and dependent on factors such as reproductive status. Mating induces many behavioral and ph...

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Autores principales: Immonen, Elina, Sayadi, Ahmed, Bayram, Helen, Arnqvist, Göran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5381559/
https://www.ncbi.nlm.nih.gov/pubmed/28391318
http://dx.doi.org/10.1093/gbe/evx029
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author Immonen, Elina
Sayadi, Ahmed
Bayram, Helen
Arnqvist, Göran
author_facet Immonen, Elina
Sayadi, Ahmed
Bayram, Helen
Arnqvist, Göran
author_sort Immonen, Elina
collection PubMed
description Sexually dimorphic phenotypes arise largely from sex-specific gene expression, which has mainly been characterized in sexually naïve adults. However, we expect sexual dimorphism in transcription to be dynamic and dependent on factors such as reproductive status. Mating induces many behavioral and physiological changes distinct to each sex and is therefore expected to activate regulatory changes in many sex-biased genes. Here, we first characterized sexual dimorphism in gene expression in Callosobruchus maculatus seed beetles. We then examined how females and males respond to mating and how it affects sex-biased expression, both in sex-limited (abdomen) and sex-shared (head and thorax) tissues. Mating responses were largely sex-specific and, as expected, females showed more genes responding compared with males (∼2,000 vs. ∼300 genes in the abdomen, ∼500 vs. ∼400 in the head and thorax, respectively). Of the sex-biased genes present in virgins, 16% (1,041 genes) in the abdomen and 17% (243 genes) in the head and thorax altered their relative expression between the sexes as a result of mating. Sex-bias status changed in 2% of the genes in the abdomen and 4% in the head and thorax following mating. Mating responses involved de-feminization of females and, to a lesser extent, de-masculinization of males relative to their virgin state: mating decreased rather than increased dimorphic expression of sex-biased genes. The fact that regulatory changes of both types of sex-biased genes occurred in both sexes suggests that male- and female-specific selection is not restricted to male- and female-biased genes, respectively, as is sometimes assumed.
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spelling pubmed-53815592017-11-07 Mating Changes Sexually Dimorphic Gene Expression in the Seed Beetle Callosobruchus maculatus Immonen, Elina Sayadi, Ahmed Bayram, Helen Arnqvist, Göran Genome Biol Evol Research Article Sexually dimorphic phenotypes arise largely from sex-specific gene expression, which has mainly been characterized in sexually naïve adults. However, we expect sexual dimorphism in transcription to be dynamic and dependent on factors such as reproductive status. Mating induces many behavioral and physiological changes distinct to each sex and is therefore expected to activate regulatory changes in many sex-biased genes. Here, we first characterized sexual dimorphism in gene expression in Callosobruchus maculatus seed beetles. We then examined how females and males respond to mating and how it affects sex-biased expression, both in sex-limited (abdomen) and sex-shared (head and thorax) tissues. Mating responses were largely sex-specific and, as expected, females showed more genes responding compared with males (∼2,000 vs. ∼300 genes in the abdomen, ∼500 vs. ∼400 in the head and thorax, respectively). Of the sex-biased genes present in virgins, 16% (1,041 genes) in the abdomen and 17% (243 genes) in the head and thorax altered their relative expression between the sexes as a result of mating. Sex-bias status changed in 2% of the genes in the abdomen and 4% in the head and thorax following mating. Mating responses involved de-feminization of females and, to a lesser extent, de-masculinization of males relative to their virgin state: mating decreased rather than increased dimorphic expression of sex-biased genes. The fact that regulatory changes of both types of sex-biased genes occurred in both sexes suggests that male- and female-specific selection is not restricted to male- and female-biased genes, respectively, as is sometimes assumed. Oxford University Press 2017-03-01 /pmc/articles/PMC5381559/ /pubmed/28391318 http://dx.doi.org/10.1093/gbe/evx029 Text en © The Author(s) 2017. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Article
Immonen, Elina
Sayadi, Ahmed
Bayram, Helen
Arnqvist, Göran
Mating Changes Sexually Dimorphic Gene Expression in the Seed Beetle Callosobruchus maculatus
title Mating Changes Sexually Dimorphic Gene Expression in the Seed Beetle Callosobruchus maculatus
title_full Mating Changes Sexually Dimorphic Gene Expression in the Seed Beetle Callosobruchus maculatus
title_fullStr Mating Changes Sexually Dimorphic Gene Expression in the Seed Beetle Callosobruchus maculatus
title_full_unstemmed Mating Changes Sexually Dimorphic Gene Expression in the Seed Beetle Callosobruchus maculatus
title_short Mating Changes Sexually Dimorphic Gene Expression in the Seed Beetle Callosobruchus maculatus
title_sort mating changes sexually dimorphic gene expression in the seed beetle callosobruchus maculatus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5381559/
https://www.ncbi.nlm.nih.gov/pubmed/28391318
http://dx.doi.org/10.1093/gbe/evx029
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