Cargando…

Mating system manipulation and the evolution of sex-biased gene expression in Drosophila

Sex differences in dioecious animals are pervasive and result from gene expression differences. Elevated sexual selection has been predicted to increase the number and expression of male-biased genes, and experimentally imposing monogamy on Drosophila melanogaster has led to a relative feminisation...

Descripción completa

Detalles Bibliográficos
Autores principales: Veltsos, Paris, Fang, Yongxiang, Cossins, Andrew R., Snook, Rhonda R., Ritchie, Michael G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727229/
https://www.ncbi.nlm.nih.gov/pubmed/29233985
http://dx.doi.org/10.1038/s41467-017-02232-6
_version_ 1783285836008128512
author Veltsos, Paris
Fang, Yongxiang
Cossins, Andrew R.
Snook, Rhonda R.
Ritchie, Michael G.
author_facet Veltsos, Paris
Fang, Yongxiang
Cossins, Andrew R.
Snook, Rhonda R.
Ritchie, Michael G.
author_sort Veltsos, Paris
collection PubMed
description Sex differences in dioecious animals are pervasive and result from gene expression differences. Elevated sexual selection has been predicted to increase the number and expression of male-biased genes, and experimentally imposing monogamy on Drosophila melanogaster has led to a relative feminisation of the transcriptome. Here, we test this hypothesis further by subjecting another polyandrous species, D. pseudoobscura, to 150 generations of experimental monogamy or elevated polyandry. We find that sex-biased genes do change in expression but, contrary to predictions, there is usually masculinisation of the transcriptome under monogamy, although this depends on tissue and sex. We also identify and describe gene expression changes following courtship experience. Courtship often influences gene expression, including patterns in sex-biased gene expression. Our results confirm that mating system manipulation disproportionately influences sex-biased gene expression but show that the direction of change is dynamic and unpredictable.
format Online
Article
Text
id pubmed-5727229
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-57272292017-12-14 Mating system manipulation and the evolution of sex-biased gene expression in Drosophila Veltsos, Paris Fang, Yongxiang Cossins, Andrew R. Snook, Rhonda R. Ritchie, Michael G. Nat Commun Article Sex differences in dioecious animals are pervasive and result from gene expression differences. Elevated sexual selection has been predicted to increase the number and expression of male-biased genes, and experimentally imposing monogamy on Drosophila melanogaster has led to a relative feminisation of the transcriptome. Here, we test this hypothesis further by subjecting another polyandrous species, D. pseudoobscura, to 150 generations of experimental monogamy or elevated polyandry. We find that sex-biased genes do change in expression but, contrary to predictions, there is usually masculinisation of the transcriptome under monogamy, although this depends on tissue and sex. We also identify and describe gene expression changes following courtship experience. Courtship often influences gene expression, including patterns in sex-biased gene expression. Our results confirm that mating system manipulation disproportionately influences sex-biased gene expression but show that the direction of change is dynamic and unpredictable. Nature Publishing Group UK 2017-12-12 /pmc/articles/PMC5727229/ /pubmed/29233985 http://dx.doi.org/10.1038/s41467-017-02232-6 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Veltsos, Paris
Fang, Yongxiang
Cossins, Andrew R.
Snook, Rhonda R.
Ritchie, Michael G.
Mating system manipulation and the evolution of sex-biased gene expression in Drosophila
title Mating system manipulation and the evolution of sex-biased gene expression in Drosophila
title_full Mating system manipulation and the evolution of sex-biased gene expression in Drosophila
title_fullStr Mating system manipulation and the evolution of sex-biased gene expression in Drosophila
title_full_unstemmed Mating system manipulation and the evolution of sex-biased gene expression in Drosophila
title_short Mating system manipulation and the evolution of sex-biased gene expression in Drosophila
title_sort mating system manipulation and the evolution of sex-biased gene expression in drosophila
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727229/
https://www.ncbi.nlm.nih.gov/pubmed/29233985
http://dx.doi.org/10.1038/s41467-017-02232-6
work_keys_str_mv AT veltsosparis matingsystemmanipulationandtheevolutionofsexbiasedgeneexpressionindrosophila
AT fangyongxiang matingsystemmanipulationandtheevolutionofsexbiasedgeneexpressionindrosophila
AT cossinsandrewr matingsystemmanipulationandtheevolutionofsexbiasedgeneexpressionindrosophila
AT snookrhondar matingsystemmanipulationandtheevolutionofsexbiasedgeneexpressionindrosophila
AT ritchiemichaelg matingsystemmanipulationandtheevolutionofsexbiasedgeneexpressionindrosophila