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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...

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Autores principales: Malacrinò, Antonino, Brengdahl, Martin I., Kimber, Christopher M., Mital, Avani, Shenoi, Vinesh N., Mirabello, Claudio, Friberg, Urban
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2022
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.
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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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