Cargando…
Inbreeding removes sex differences in lifespan in a population of Drosophila melanogaster
Sex differences in ageing rates and lifespan are common in nature, and an enduring puzzle for evolutionary biology. One possibility is that sex-specific mortality rates may result from recessive deleterious alleles in ‘unguarded’ heterogametic X or Z sex chromosomes (the unguarded X hypothesis). Emp...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4938057/ https://www.ncbi.nlm.nih.gov/pubmed/27354712 http://dx.doi.org/10.1098/rsbl.2016.0337 |
_version_ | 1782441809067114496 |
---|---|
author | Carazo, Pau Green, Jared Sepil, Irem Pizzari, Tommaso Wigby, Stuart |
author_facet | Carazo, Pau Green, Jared Sepil, Irem Pizzari, Tommaso Wigby, Stuart |
author_sort | Carazo, Pau |
collection | PubMed |
description | Sex differences in ageing rates and lifespan are common in nature, and an enduring puzzle for evolutionary biology. One possibility is that sex-specific mortality rates may result from recessive deleterious alleles in ‘unguarded’ heterogametic X or Z sex chromosomes (the unguarded X hypothesis). Empirical evidence for this is, however, limited. Here, we test a fundamental prediction of the unguarded X hypothesis in Drosophila melanogaster, namely that inbreeding shortens lifespan more in females (the homogametic sex in Drosophila) than in males. To test for additional sex-specific social effects, we studied the lifespan of males and females kept in isolation, in related same-sex groups, and in unrelated same-sex groups. As expected, outbred females outlived outbred males and inbreeding shortened lifespan. However, inbreeding-mediated reductions in lifespan were stronger for females, such that lifespan was similar in inbred females and males. We also show that the social environment, independent of inbreeding, affected male, but not female lifespan. In conjunction with recent studies, the present results suggest that asymmetric inheritance mechanisms may play an important role in the evolution of sex-specific lifespan and that social effects must be considered explicitly when studying these fundamental patterns. |
format | Online Article Text |
id | pubmed-4938057 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-49380572016-07-15 Inbreeding removes sex differences in lifespan in a population of Drosophila melanogaster Carazo, Pau Green, Jared Sepil, Irem Pizzari, Tommaso Wigby, Stuart Biol Lett Evolutionary Biology Sex differences in ageing rates and lifespan are common in nature, and an enduring puzzle for evolutionary biology. One possibility is that sex-specific mortality rates may result from recessive deleterious alleles in ‘unguarded’ heterogametic X or Z sex chromosomes (the unguarded X hypothesis). Empirical evidence for this is, however, limited. Here, we test a fundamental prediction of the unguarded X hypothesis in Drosophila melanogaster, namely that inbreeding shortens lifespan more in females (the homogametic sex in Drosophila) than in males. To test for additional sex-specific social effects, we studied the lifespan of males and females kept in isolation, in related same-sex groups, and in unrelated same-sex groups. As expected, outbred females outlived outbred males and inbreeding shortened lifespan. However, inbreeding-mediated reductions in lifespan were stronger for females, such that lifespan was similar in inbred females and males. We also show that the social environment, independent of inbreeding, affected male, but not female lifespan. In conjunction with recent studies, the present results suggest that asymmetric inheritance mechanisms may play an important role in the evolution of sex-specific lifespan and that social effects must be considered explicitly when studying these fundamental patterns. The Royal Society 2016-06 /pmc/articles/PMC4938057/ /pubmed/27354712 http://dx.doi.org/10.1098/rsbl.2016.0337 Text en © 2016 The Authors. http://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/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Evolutionary Biology Carazo, Pau Green, Jared Sepil, Irem Pizzari, Tommaso Wigby, Stuart Inbreeding removes sex differences in lifespan in a population of Drosophila melanogaster |
title | Inbreeding removes sex differences in lifespan in a population of Drosophila melanogaster |
title_full | Inbreeding removes sex differences in lifespan in a population of Drosophila melanogaster |
title_fullStr | Inbreeding removes sex differences in lifespan in a population of Drosophila melanogaster |
title_full_unstemmed | Inbreeding removes sex differences in lifespan in a population of Drosophila melanogaster |
title_short | Inbreeding removes sex differences in lifespan in a population of Drosophila melanogaster |
title_sort | inbreeding removes sex differences in lifespan in a population of drosophila melanogaster |
topic | Evolutionary Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4938057/ https://www.ncbi.nlm.nih.gov/pubmed/27354712 http://dx.doi.org/10.1098/rsbl.2016.0337 |
work_keys_str_mv | AT carazopau inbreedingremovessexdifferencesinlifespaninapopulationofdrosophilamelanogaster AT greenjared inbreedingremovessexdifferencesinlifespaninapopulationofdrosophilamelanogaster AT sepilirem inbreedingremovessexdifferencesinlifespaninapopulationofdrosophilamelanogaster AT pizzaritommaso inbreedingremovessexdifferencesinlifespaninapopulationofdrosophilamelanogaster AT wigbystuart inbreedingremovessexdifferencesinlifespaninapopulationofdrosophilamelanogaster |