Cargando…

Sexual conflict over remating interval is modulated by the sex peptide pathway

Sexual conflict, in which the evolutionary interests of males and females diverge, shapes the evolution of reproductive systems across diverse taxa. Here, we used the fruit fly to study sexual conflict in natural, three-way interactions comprising a female, her current and previous mates. We manipul...

Descripción completa

Detalles Bibliográficos
Autores principales: Smith, Damian T., Clarke, Naomi V. E., Boone, James M., Fricke, Claudia, Chapman, Tracey
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5360916/
https://www.ncbi.nlm.nih.gov/pubmed/28250180
http://dx.doi.org/10.1098/rspb.2016.2394
_version_ 1782516666521878528
author Smith, Damian T.
Clarke, Naomi V. E.
Boone, James M.
Fricke, Claudia
Chapman, Tracey
author_facet Smith, Damian T.
Clarke, Naomi V. E.
Boone, James M.
Fricke, Claudia
Chapman, Tracey
author_sort Smith, Damian T.
collection PubMed
description Sexual conflict, in which the evolutionary interests of males and females diverge, shapes the evolution of reproductive systems across diverse taxa. Here, we used the fruit fly to study sexual conflict in natural, three-way interactions comprising a female, her current and previous mates. We manipulated the potential for sexual conflict by using sex peptide receptor (SPR) null females and by varying remating from 3 to 48 h, a period during which natural rematings frequently occur. SPR-lacking females do not respond to sex peptide (SP) transferred during mating and maintain virgin levels of high receptivity and low fecundity. In the absence of SPR, there was a convergence of fitness interests, with all individuals gaining highest productivity at 5 h remating. This suggests that the expression of sexual conflict was reduced. We observed an unexpected second male-specific advantage to early remating, resulting from an increase in the efficiency of second male sperm use. This early window of opportunity for exploitation by second males depended on the presence of SPR. The results suggest that the SP pathway can modulate the expression of sexual conflict in this system, and show how variation in the selective forces that shape conflict and cooperation can be maintained.
format Online
Article
Text
id pubmed-5360916
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher The Royal Society
record_format MEDLINE/PubMed
spelling pubmed-53609162017-03-31 Sexual conflict over remating interval is modulated by the sex peptide pathway Smith, Damian T. Clarke, Naomi V. E. Boone, James M. Fricke, Claudia Chapman, Tracey Proc Biol Sci Ecology Sexual conflict, in which the evolutionary interests of males and females diverge, shapes the evolution of reproductive systems across diverse taxa. Here, we used the fruit fly to study sexual conflict in natural, three-way interactions comprising a female, her current and previous mates. We manipulated the potential for sexual conflict by using sex peptide receptor (SPR) null females and by varying remating from 3 to 48 h, a period during which natural rematings frequently occur. SPR-lacking females do not respond to sex peptide (SP) transferred during mating and maintain virgin levels of high receptivity and low fecundity. In the absence of SPR, there was a convergence of fitness interests, with all individuals gaining highest productivity at 5 h remating. This suggests that the expression of sexual conflict was reduced. We observed an unexpected second male-specific advantage to early remating, resulting from an increase in the efficiency of second male sperm use. This early window of opportunity for exploitation by second males depended on the presence of SPR. The results suggest that the SP pathway can modulate the expression of sexual conflict in this system, and show how variation in the selective forces that shape conflict and cooperation can be maintained. The Royal Society 2017-03-15 2017-03-01 /pmc/articles/PMC5360916/ /pubmed/28250180 http://dx.doi.org/10.1098/rspb.2016.2394 Text en © 2017 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 Ecology
Smith, Damian T.
Clarke, Naomi V. E.
Boone, James M.
Fricke, Claudia
Chapman, Tracey
Sexual conflict over remating interval is modulated by the sex peptide pathway
title Sexual conflict over remating interval is modulated by the sex peptide pathway
title_full Sexual conflict over remating interval is modulated by the sex peptide pathway
title_fullStr Sexual conflict over remating interval is modulated by the sex peptide pathway
title_full_unstemmed Sexual conflict over remating interval is modulated by the sex peptide pathway
title_short Sexual conflict over remating interval is modulated by the sex peptide pathway
title_sort sexual conflict over remating interval is modulated by the sex peptide pathway
topic Ecology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5360916/
https://www.ncbi.nlm.nih.gov/pubmed/28250180
http://dx.doi.org/10.1098/rspb.2016.2394
work_keys_str_mv AT smithdamiant sexualconflictoverrematingintervalismodulatedbythesexpeptidepathway
AT clarkenaomive sexualconflictoverrematingintervalismodulatedbythesexpeptidepathway
AT boonejamesm sexualconflictoverrematingintervalismodulatedbythesexpeptidepathway
AT frickeclaudia sexualconflictoverrematingintervalismodulatedbythesexpeptidepathway
AT chapmantracey sexualconflictoverrematingintervalismodulatedbythesexpeptidepathway