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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...

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Autores principales: McDonough-Goldstein, Caitlin E, Borziak, Kirill, Pitnick, Scott, Dorus, Steve
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
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.
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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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