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Drosophila female reproductive tract gene expression reveals coordinated mating responses and rapidly evolving tissue-specific genes
Sexual reproduction in internally fertilizing species requires complex coordination between female and male reproductive systems and among the diverse tissues of the female reproductive tract (FRT). Here, we report a comprehensive, tissue-specific investigation of Drosophila melanogaster FRT gene ex...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8063083/ https://www.ncbi.nlm.nih.gov/pubmed/33890615 http://dx.doi.org/10.1093/g3journal/jkab020 |
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author | McDonough-Goldstein, Caitlin E Borziak, Kirill Pitnick, Scott Dorus, Steve |
author_facet | McDonough-Goldstein, Caitlin E Borziak, Kirill Pitnick, Scott Dorus, Steve |
author_sort | McDonough-Goldstein, Caitlin E |
collection | PubMed |
description | Sexual reproduction in internally fertilizing species requires complex coordination between female and male reproductive systems and among the diverse tissues of the female reproductive tract (FRT). Here, we report a comprehensive, tissue-specific investigation of Drosophila melanogaster FRT gene expression before and after mating. We identified expression profiles that distinguished each tissue, including major differences between tissues with glandular or primarily nonglandular epithelium. All tissues were enriched for distinct sets of genes possessing secretion signals that exhibited accelerated evolution, as might be expected for genes participating in molecular interactions between the sexes within the FRT extracellular environment. Despite robust transcriptional differences between tissues, postmating responses were dominated by coordinated transient changes indicative of an integrated systems-level functional response. This comprehensive characterization of gene expression throughout the FRT identifies putative female contributions to postcopulatory events critical to reproduction and potentially reproductive isolation, as well as the putative targets of sexual selection and conflict. |
format | Online Article Text |
id | pubmed-8063083 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-80630832021-04-29 Drosophila female reproductive tract gene expression reveals coordinated mating responses and rapidly evolving tissue-specific genes McDonough-Goldstein, Caitlin E Borziak, Kirill Pitnick, Scott Dorus, Steve G3 (Bethesda) Investigation Sexual reproduction in internally fertilizing species requires complex coordination between female and male reproductive systems and among the diverse tissues of the female reproductive tract (FRT). Here, we report a comprehensive, tissue-specific investigation of Drosophila melanogaster FRT gene expression before and after mating. We identified expression profiles that distinguished each tissue, including major differences between tissues with glandular or primarily nonglandular epithelium. All tissues were enriched for distinct sets of genes possessing secretion signals that exhibited accelerated evolution, as might be expected for genes participating in molecular interactions between the sexes within the FRT extracellular environment. Despite robust transcriptional differences between tissues, postmating responses were dominated by coordinated transient changes indicative of an integrated systems-level functional response. This comprehensive characterization of gene expression throughout the FRT identifies putative female contributions to postcopulatory events critical to reproduction and potentially reproductive isolation, as well as the putative targets of sexual selection and conflict. Oxford University Press 2021-01-28 /pmc/articles/PMC8063083/ /pubmed/33890615 http://dx.doi.org/10.1093/g3journal/jkab020 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Genetics Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Investigation McDonough-Goldstein, Caitlin E Borziak, Kirill Pitnick, Scott Dorus, Steve Drosophila female reproductive tract gene expression reveals coordinated mating responses and rapidly evolving tissue-specific genes |
title |
Drosophila female reproductive tract gene expression reveals coordinated mating responses and rapidly evolving tissue-specific genes |
title_full |
Drosophila female reproductive tract gene expression reveals coordinated mating responses and rapidly evolving tissue-specific genes |
title_fullStr |
Drosophila female reproductive tract gene expression reveals coordinated mating responses and rapidly evolving tissue-specific genes |
title_full_unstemmed |
Drosophila female reproductive tract gene expression reveals coordinated mating responses and rapidly evolving tissue-specific genes |
title_short |
Drosophila female reproductive tract gene expression reveals coordinated mating responses and rapidly evolving tissue-specific genes |
title_sort | drosophila female reproductive tract gene expression reveals coordinated mating responses and rapidly evolving tissue-specific genes |
topic | Investigation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8063083/ https://www.ncbi.nlm.nih.gov/pubmed/33890615 http://dx.doi.org/10.1093/g3journal/jkab020 |
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