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Sex differences in the genetic architecture of lifespan in a seed beetle: extreme inbreeding extends male lifespan
BACKGROUND: Sex differences in lifespan are ubiquitous throughout the animal kingdom but the causes underlying this phenomenon remain poorly understood. Several explanations based on asymmetrical inheritance patterns (sex chromosomes or mitochondrial DNA) have been proposed, but these ideas have rar...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2657122/ https://www.ncbi.nlm.nih.gov/pubmed/19200350 http://dx.doi.org/10.1186/1471-2148-9-33 |
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author | Bilde, Trine Maklakov, Alexei A Meisner, Katrine la Guardia, Lucia Friberg, Urban |
author_facet | Bilde, Trine Maklakov, Alexei A Meisner, Katrine la Guardia, Lucia Friberg, Urban |
author_sort | Bilde, Trine |
collection | PubMed |
description | BACKGROUND: Sex differences in lifespan are ubiquitous throughout the animal kingdom but the causes underlying this phenomenon remain poorly understood. Several explanations based on asymmetrical inheritance patterns (sex chromosomes or mitochondrial DNA) have been proposed, but these ideas have rarely been tested experimentally. Alternatively, sexual dimorphism in lifespan could result from sex-specific selection, caused by fundamental differences in how males and females optimize their fitness by allocating resources into current and future reproduction. RESULTS: Here we used sex-specific responses to inbreeding to study the genetic architecture of lifespan and mortality rates in Callosobruchus maculatus, a seed beetle that shows sexual dimorphism in lifespan. Two independent assays revealed opposing sex-specific responses to inbreeding. The combined data set showed that inbred males live longer than outbred males, while females show the opposite pattern. Both sexes suffered reduced fitness measured as lifetime reproductive success as a result of inbreeding. CONCLUSION: No model based on asymmetrical inheritance can explain increased male lifespan in response to inbreeding. Our results are however compatible with models based on sex-specific selection on reproductive strategies. We therefore suggest that sex-specific differences in lifespan in this species primarily result from sexually divergent selection. |
format | Text |
id | pubmed-2657122 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-26571222009-03-18 Sex differences in the genetic architecture of lifespan in a seed beetle: extreme inbreeding extends male lifespan Bilde, Trine Maklakov, Alexei A Meisner, Katrine la Guardia, Lucia Friberg, Urban BMC Evol Biol Research Article BACKGROUND: Sex differences in lifespan are ubiquitous throughout the animal kingdom but the causes underlying this phenomenon remain poorly understood. Several explanations based on asymmetrical inheritance patterns (sex chromosomes or mitochondrial DNA) have been proposed, but these ideas have rarely been tested experimentally. Alternatively, sexual dimorphism in lifespan could result from sex-specific selection, caused by fundamental differences in how males and females optimize their fitness by allocating resources into current and future reproduction. RESULTS: Here we used sex-specific responses to inbreeding to study the genetic architecture of lifespan and mortality rates in Callosobruchus maculatus, a seed beetle that shows sexual dimorphism in lifespan. Two independent assays revealed opposing sex-specific responses to inbreeding. The combined data set showed that inbred males live longer than outbred males, while females show the opposite pattern. Both sexes suffered reduced fitness measured as lifetime reproductive success as a result of inbreeding. CONCLUSION: No model based on asymmetrical inheritance can explain increased male lifespan in response to inbreeding. Our results are however compatible with models based on sex-specific selection on reproductive strategies. We therefore suggest that sex-specific differences in lifespan in this species primarily result from sexually divergent selection. BioMed Central 2009-02-06 /pmc/articles/PMC2657122/ /pubmed/19200350 http://dx.doi.org/10.1186/1471-2148-9-33 Text en Copyright © 2009 Bilde et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Bilde, Trine Maklakov, Alexei A Meisner, Katrine la Guardia, Lucia Friberg, Urban Sex differences in the genetic architecture of lifespan in a seed beetle: extreme inbreeding extends male lifespan |
title | Sex differences in the genetic architecture of lifespan in a seed beetle: extreme inbreeding extends male lifespan |
title_full | Sex differences in the genetic architecture of lifespan in a seed beetle: extreme inbreeding extends male lifespan |
title_fullStr | Sex differences in the genetic architecture of lifespan in a seed beetle: extreme inbreeding extends male lifespan |
title_full_unstemmed | Sex differences in the genetic architecture of lifespan in a seed beetle: extreme inbreeding extends male lifespan |
title_short | Sex differences in the genetic architecture of lifespan in a seed beetle: extreme inbreeding extends male lifespan |
title_sort | sex differences in the genetic architecture of lifespan in a seed beetle: extreme inbreeding extends male lifespan |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2657122/ https://www.ncbi.nlm.nih.gov/pubmed/19200350 http://dx.doi.org/10.1186/1471-2148-9-33 |
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