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Ageing desexualizes the Drosophila brain transcriptome
General evolutionary theory predicts that individuals in low condition should invest less in sexual traits compared to individuals in high condition. Whether this positive association between condition and investment also holds between young (high condition) and senesced (low condition) individuals...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9364003/ https://www.ncbi.nlm.nih.gov/pubmed/35946149 http://dx.doi.org/10.1098/rspb.2022.1115 |
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author | Malacrinò, Antonino Brengdahl, Martin I. Kimber, Christopher M. Mital, Avani Shenoi, Vinesh N. Mirabello, Claudio Friberg, Urban |
author_facet | Malacrinò, Antonino Brengdahl, Martin I. Kimber, Christopher M. Mital, Avani Shenoi, Vinesh N. Mirabello, Claudio Friberg, Urban |
author_sort | Malacrinò, Antonino |
collection | PubMed |
description | General evolutionary theory predicts that individuals in low condition should invest less in sexual traits compared to individuals in high condition. Whether this positive association between condition and investment also holds between young (high condition) and senesced (low condition) individuals is however less clear, since elevated investment into reproduction may be beneficial when individuals approach the end of their life. To address how investment into sexual traits changes with age, we study genes with sex-biased expression in the brain, the tissue from which sexual behaviours are directed. Across two distinct populations of Drosophila melanogaster, we find that old brains display fewer sex-biased genes, and that expression of both male-biased and female-biased genes converges towards a sexually intermediate phenotype owing to changes in both sexes with age. We further find that sex-biased genes in general show heightened age-dependent expression in comparison to unbiased genes and that age-related changes in the sexual brain transcriptome are commonly larger in males than females. Our results hence show that ageing causes a desexualization of the fruit fly brain transcriptome and that this change mirrors the general prediction that low condition individuals should invest less in sexual phenotypes. |
format | Online Article Text |
id | pubmed-9364003 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-93640032022-08-12 Ageing desexualizes the Drosophila brain transcriptome Malacrinò, Antonino Brengdahl, Martin I. Kimber, Christopher M. Mital, Avani Shenoi, Vinesh N. Mirabello, Claudio Friberg, Urban Proc Biol Sci Evolution General evolutionary theory predicts that individuals in low condition should invest less in sexual traits compared to individuals in high condition. Whether this positive association between condition and investment also holds between young (high condition) and senesced (low condition) individuals is however less clear, since elevated investment into reproduction may be beneficial when individuals approach the end of their life. To address how investment into sexual traits changes with age, we study genes with sex-biased expression in the brain, the tissue from which sexual behaviours are directed. Across two distinct populations of Drosophila melanogaster, we find that old brains display fewer sex-biased genes, and that expression of both male-biased and female-biased genes converges towards a sexually intermediate phenotype owing to changes in both sexes with age. We further find that sex-biased genes in general show heightened age-dependent expression in comparison to unbiased genes and that age-related changes in the sexual brain transcriptome are commonly larger in males than females. Our results hence show that ageing causes a desexualization of the fruit fly brain transcriptome and that this change mirrors the general prediction that low condition individuals should invest less in sexual phenotypes. The Royal Society 2022-08-10 2022-08-10 /pmc/articles/PMC9364003/ /pubmed/35946149 http://dx.doi.org/10.1098/rspb.2022.1115 Text en © 2022 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society 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 use, provided the original author and source are credited. |
spellingShingle | Evolution Malacrinò, Antonino Brengdahl, Martin I. Kimber, Christopher M. Mital, Avani Shenoi, Vinesh N. Mirabello, Claudio Friberg, Urban Ageing desexualizes the Drosophila brain transcriptome |
title | Ageing desexualizes the Drosophila brain transcriptome |
title_full | Ageing desexualizes the Drosophila brain transcriptome |
title_fullStr | Ageing desexualizes the Drosophila brain transcriptome |
title_full_unstemmed | Ageing desexualizes the Drosophila brain transcriptome |
title_short | Ageing desexualizes the Drosophila brain transcriptome |
title_sort | ageing desexualizes the drosophila brain transcriptome |
topic | Evolution |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9364003/ https://www.ncbi.nlm.nih.gov/pubmed/35946149 http://dx.doi.org/10.1098/rspb.2022.1115 |
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