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Experimental sexual selection reveals rapid evolutionary divergence in sex‐specific transcriptomes and their interactions following mating
Post copulatory interactions between the sexes in internally fertilizing species elicits both sexual conflict and sexual selection. Macroevolutionary and comparative studies have linked these processes to rapid transcriptomic evolution in sex‐specific tissues and substantial transcriptomic post mati...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9325514/ https://www.ncbi.nlm.nih.gov/pubmed/35437824 http://dx.doi.org/10.1111/mec.16473 |
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author | Veltsos, Paris Porcelli, Damiano Fang, Yongxiang Cossins, Andrew R. Ritchie, Michael G. Snook, Rhonda R. |
author_facet | Veltsos, Paris Porcelli, Damiano Fang, Yongxiang Cossins, Andrew R. Ritchie, Michael G. Snook, Rhonda R. |
author_sort | Veltsos, Paris |
collection | PubMed |
description | Post copulatory interactions between the sexes in internally fertilizing species elicits both sexual conflict and sexual selection. Macroevolutionary and comparative studies have linked these processes to rapid transcriptomic evolution in sex‐specific tissues and substantial transcriptomic post mating responses in females, patterns of which are altered when mating between reproductively isolated species. Here, we tested multiple predictions arising from sexual selection and conflict theory about the evolution of sex‐specific and tissue‐specific gene expression and the post mating response at the microevolutionary level. Following over 150 generations of experimental evolution under either reduced (enforced monogamy) or elevated (polyandry) sexual selection in Drosophila pseudoobscura, we found a substantial effect of sexual selection treatment on transcriptomic divergence in virgin male and female reproductive tissues (testes, male accessory glands, the female reproductive tract and ovaries). Sexual selection treatment also had a dominant effect on the post mating response, particularly in the female reproductive tract – the main arena for sexual conflict – compared to ovaries. This effect was asymmetric with monandry females typically showing more post mating responses than polyandry females, with enriched gene functions varying across treatments. The evolutionary history of the male partner had a larger effect on the post mating response of monandry females, but females from both sexual selection treatments showed unique patterns of gene expression and gene function when mating with males from the alternate treatment. Our microevolutionary results mostly confirm comparative macroevolutionary predictions on the role of sexual selection on transcriptomic divergence and altered gene regulation arising from divergent coevolutionary trajectories between sexual selection treatments. |
format | Online Article Text |
id | pubmed-9325514 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93255142022-07-30 Experimental sexual selection reveals rapid evolutionary divergence in sex‐specific transcriptomes and their interactions following mating Veltsos, Paris Porcelli, Damiano Fang, Yongxiang Cossins, Andrew R. Ritchie, Michael G. Snook, Rhonda R. Mol Ecol ORIGINAL ARTICLES Post copulatory interactions between the sexes in internally fertilizing species elicits both sexual conflict and sexual selection. Macroevolutionary and comparative studies have linked these processes to rapid transcriptomic evolution in sex‐specific tissues and substantial transcriptomic post mating responses in females, patterns of which are altered when mating between reproductively isolated species. Here, we tested multiple predictions arising from sexual selection and conflict theory about the evolution of sex‐specific and tissue‐specific gene expression and the post mating response at the microevolutionary level. Following over 150 generations of experimental evolution under either reduced (enforced monogamy) or elevated (polyandry) sexual selection in Drosophila pseudoobscura, we found a substantial effect of sexual selection treatment on transcriptomic divergence in virgin male and female reproductive tissues (testes, male accessory glands, the female reproductive tract and ovaries). Sexual selection treatment also had a dominant effect on the post mating response, particularly in the female reproductive tract – the main arena for sexual conflict – compared to ovaries. This effect was asymmetric with monandry females typically showing more post mating responses than polyandry females, with enriched gene functions varying across treatments. The evolutionary history of the male partner had a larger effect on the post mating response of monandry females, but females from both sexual selection treatments showed unique patterns of gene expression and gene function when mating with males from the alternate treatment. Our microevolutionary results mostly confirm comparative macroevolutionary predictions on the role of sexual selection on transcriptomic divergence and altered gene regulation arising from divergent coevolutionary trajectories between sexual selection treatments. John Wiley and Sons Inc. 2022-04-28 2022-06 /pmc/articles/PMC9325514/ /pubmed/35437824 http://dx.doi.org/10.1111/mec.16473 Text en © 2022 The Authors. Molecular Ecology published by John Wiley & Sons Ltd. 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 | ORIGINAL ARTICLES Veltsos, Paris Porcelli, Damiano Fang, Yongxiang Cossins, Andrew R. Ritchie, Michael G. Snook, Rhonda R. Experimental sexual selection reveals rapid evolutionary divergence in sex‐specific transcriptomes and their interactions following mating |
title | Experimental sexual selection reveals rapid evolutionary divergence in sex‐specific transcriptomes and their interactions following mating |
title_full | Experimental sexual selection reveals rapid evolutionary divergence in sex‐specific transcriptomes and their interactions following mating |
title_fullStr | Experimental sexual selection reveals rapid evolutionary divergence in sex‐specific transcriptomes and their interactions following mating |
title_full_unstemmed | Experimental sexual selection reveals rapid evolutionary divergence in sex‐specific transcriptomes and their interactions following mating |
title_short | Experimental sexual selection reveals rapid evolutionary divergence in sex‐specific transcriptomes and their interactions following mating |
title_sort | experimental sexual selection reveals rapid evolutionary divergence in sex‐specific transcriptomes and their interactions following mating |
topic | ORIGINAL ARTICLES |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9325514/ https://www.ncbi.nlm.nih.gov/pubmed/35437824 http://dx.doi.org/10.1111/mec.16473 |
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