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Gene expression and alternative splicing dynamics are perturbed in female head transcriptomes following heterospecific copulation
BACKGROUND: Despite the growing interest in the female side of copulatory interactions, the roles played by differential expression and alternative splicing mechanisms of pre-RNA on tissues outside of the reproductive tract have remained largely unknown. Here we addressed these questions in the cont...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8132402/ https://www.ncbi.nlm.nih.gov/pubmed/34006224 http://dx.doi.org/10.1186/s12864-021-07669-0 |
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author | Diaz, Fernando Allan, Carson W. Markow, Therese Ann Bono, Jeremy M. Matzkin, Luciano M. |
author_facet | Diaz, Fernando Allan, Carson W. Markow, Therese Ann Bono, Jeremy M. Matzkin, Luciano M. |
author_sort | Diaz, Fernando |
collection | PubMed |
description | BACKGROUND: Despite the growing interest in the female side of copulatory interactions, the roles played by differential expression and alternative splicing mechanisms of pre-RNA on tissues outside of the reproductive tract have remained largely unknown. Here we addressed these questions in the context of con- vs heterospecific matings between Drosophila mojavensis and its sister species, D. arizonae. We analyzed transcriptional responses in female heads using an integrated investigation of genome-wide patterns of gene expression, including differential expression (DE), alternative splicing (AS) and intron retention (IR). RESULTS: Our results indicated that early transcriptional responses were largely congruent between con- and heterospecific matings but are substantially perturbed over time. Conspecific matings induced functional pathways related to amino acid balance previously associated with the brain’s physiology and female postmating behavior. Heterospecific matings often failed to activate regulation of some of these genes and induced expression of additional genes when compared with those of conspecifically-mated females. These mechanisms showed functional specializations with DE genes mostly linked to pathways of proteolysis and nutrient homeostasis, while AS genes were more related to photoreception and muscle assembly pathways. IR seems to play a more general role in DE regulation during the female postmating response. CONCLUSIONS: We provide evidence showing that AS genes substantially perturbed by heterospecific matings in female heads evolve at slower evolutionary rates than the genome background. However, DE genes evolve at evolutionary rates similar, or even higher, than those of male reproductive genes, which highlights their potential role in sexual selection and the evolution of reproductive barriers. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-021-07669-0. |
format | Online Article Text |
id | pubmed-8132402 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-81324022021-05-19 Gene expression and alternative splicing dynamics are perturbed in female head transcriptomes following heterospecific copulation Diaz, Fernando Allan, Carson W. Markow, Therese Ann Bono, Jeremy M. Matzkin, Luciano M. BMC Genomics Research BACKGROUND: Despite the growing interest in the female side of copulatory interactions, the roles played by differential expression and alternative splicing mechanisms of pre-RNA on tissues outside of the reproductive tract have remained largely unknown. Here we addressed these questions in the context of con- vs heterospecific matings between Drosophila mojavensis and its sister species, D. arizonae. We analyzed transcriptional responses in female heads using an integrated investigation of genome-wide patterns of gene expression, including differential expression (DE), alternative splicing (AS) and intron retention (IR). RESULTS: Our results indicated that early transcriptional responses were largely congruent between con- and heterospecific matings but are substantially perturbed over time. Conspecific matings induced functional pathways related to amino acid balance previously associated with the brain’s physiology and female postmating behavior. Heterospecific matings often failed to activate regulation of some of these genes and induced expression of additional genes when compared with those of conspecifically-mated females. These mechanisms showed functional specializations with DE genes mostly linked to pathways of proteolysis and nutrient homeostasis, while AS genes were more related to photoreception and muscle assembly pathways. IR seems to play a more general role in DE regulation during the female postmating response. CONCLUSIONS: We provide evidence showing that AS genes substantially perturbed by heterospecific matings in female heads evolve at slower evolutionary rates than the genome background. However, DE genes evolve at evolutionary rates similar, or even higher, than those of male reproductive genes, which highlights their potential role in sexual selection and the evolution of reproductive barriers. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-021-07669-0. BioMed Central 2021-05-18 /pmc/articles/PMC8132402/ /pubmed/34006224 http://dx.doi.org/10.1186/s12864-021-07669-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Diaz, Fernando Allan, Carson W. Markow, Therese Ann Bono, Jeremy M. Matzkin, Luciano M. Gene expression and alternative splicing dynamics are perturbed in female head transcriptomes following heterospecific copulation |
title | Gene expression and alternative splicing dynamics are perturbed in female head transcriptomes following heterospecific copulation |
title_full | Gene expression and alternative splicing dynamics are perturbed in female head transcriptomes following heterospecific copulation |
title_fullStr | Gene expression and alternative splicing dynamics are perturbed in female head transcriptomes following heterospecific copulation |
title_full_unstemmed | Gene expression and alternative splicing dynamics are perturbed in female head transcriptomes following heterospecific copulation |
title_short | Gene expression and alternative splicing dynamics are perturbed in female head transcriptomes following heterospecific copulation |
title_sort | gene expression and alternative splicing dynamics are perturbed in female head transcriptomes following heterospecific copulation |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8132402/ https://www.ncbi.nlm.nih.gov/pubmed/34006224 http://dx.doi.org/10.1186/s12864-021-07669-0 |
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