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Experimental evolution under hyper-promiscuity in Drosophila melanogaster

BACKGROUND: The number of partners that individuals mate with over their lifetime is a defining feature of mating systems, and variation in mate number is thought to be a major driver of sexual evolution. Although previous research has investigated the evolutionary consequences of reductions in the...

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Autores principales: Perry, Jennifer C., Joag, Richa, Hosken, David J., Wedell, Nina, Radwan, Jacek, Wigby, Stuart
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4910217/
https://www.ncbi.nlm.nih.gov/pubmed/27311887
http://dx.doi.org/10.1186/s12862-016-0699-8
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author Perry, Jennifer C.
Joag, Richa
Hosken, David J.
Wedell, Nina
Radwan, Jacek
Wigby, Stuart
author_facet Perry, Jennifer C.
Joag, Richa
Hosken, David J.
Wedell, Nina
Radwan, Jacek
Wigby, Stuart
author_sort Perry, Jennifer C.
collection PubMed
description BACKGROUND: The number of partners that individuals mate with over their lifetime is a defining feature of mating systems, and variation in mate number is thought to be a major driver of sexual evolution. Although previous research has investigated the evolutionary consequences of reductions in the number of mates, we know little about the costs and benefits of increased numbers of mates. Here, we use a genetic manipulation of mating frequency in Drosophila melanogaster to create a novel, highly promiscuous mating system. We generated D. melanogaster populations in which flies were deficient for the sex peptide receptor (SPR) gene – resulting in SPR- females that mated more frequently – and genetically-matched control populations, and allowed them to evolve for 55 generations. At several time-points during this experimental evolution, we assayed behavioural, morphological and transcriptional reproductive phenotypes expected to evolve in response to increased population mating frequencies. RESULTS: We found that males from the high mating frequency SPR- populations evolved decreased ability to inhibit the receptivity of their mates and decreased copulation duration, in line with predictions of decreased per-mating investment with increased sperm competition. Unexpectedly, SPR- population males also evolved weakly increased sex peptide (SP) gene expression. Males from SPR- populations initially (i.e., before experimental evolution) exhibited more frequent courtship and faster time until mating relative to controls, but over evolutionary time these differences diminished or reversed. CONCLUSIONS: In response to experimentally increased mating frequency, SPR- males evolved behavioural responses consistent with decreased male post-copulatory investment at each mating and decreased overall pre-copulatory performance. The trend towards increased SP gene expression might plausibly relate to functional differences in the two domains of the SP protein. Our study highlights the utility of genetic manipulations of animal social and sexual environments coupled with experimental evolution. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12862-016-0699-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-49102172016-06-17 Experimental evolution under hyper-promiscuity in Drosophila melanogaster Perry, Jennifer C. Joag, Richa Hosken, David J. Wedell, Nina Radwan, Jacek Wigby, Stuart BMC Evol Biol Research Article BACKGROUND: The number of partners that individuals mate with over their lifetime is a defining feature of mating systems, and variation in mate number is thought to be a major driver of sexual evolution. Although previous research has investigated the evolutionary consequences of reductions in the number of mates, we know little about the costs and benefits of increased numbers of mates. Here, we use a genetic manipulation of mating frequency in Drosophila melanogaster to create a novel, highly promiscuous mating system. We generated D. melanogaster populations in which flies were deficient for the sex peptide receptor (SPR) gene – resulting in SPR- females that mated more frequently – and genetically-matched control populations, and allowed them to evolve for 55 generations. At several time-points during this experimental evolution, we assayed behavioural, morphological and transcriptional reproductive phenotypes expected to evolve in response to increased population mating frequencies. RESULTS: We found that males from the high mating frequency SPR- populations evolved decreased ability to inhibit the receptivity of their mates and decreased copulation duration, in line with predictions of decreased per-mating investment with increased sperm competition. Unexpectedly, SPR- population males also evolved weakly increased sex peptide (SP) gene expression. Males from SPR- populations initially (i.e., before experimental evolution) exhibited more frequent courtship and faster time until mating relative to controls, but over evolutionary time these differences diminished or reversed. CONCLUSIONS: In response to experimentally increased mating frequency, SPR- males evolved behavioural responses consistent with decreased male post-copulatory investment at each mating and decreased overall pre-copulatory performance. The trend towards increased SP gene expression might plausibly relate to functional differences in the two domains of the SP protein. Our study highlights the utility of genetic manipulations of animal social and sexual environments coupled with experimental evolution. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12862-016-0699-8) contains supplementary material, which is available to authorized users. BioMed Central 2016-06-16 /pmc/articles/PMC4910217/ /pubmed/27311887 http://dx.doi.org/10.1186/s12862-016-0699-8 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Perry, Jennifer C.
Joag, Richa
Hosken, David J.
Wedell, Nina
Radwan, Jacek
Wigby, Stuart
Experimental evolution under hyper-promiscuity in Drosophila melanogaster
title Experimental evolution under hyper-promiscuity in Drosophila melanogaster
title_full Experimental evolution under hyper-promiscuity in Drosophila melanogaster
title_fullStr Experimental evolution under hyper-promiscuity in Drosophila melanogaster
title_full_unstemmed Experimental evolution under hyper-promiscuity in Drosophila melanogaster
title_short Experimental evolution under hyper-promiscuity in Drosophila melanogaster
title_sort experimental evolution under hyper-promiscuity in drosophila melanogaster
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4910217/
https://www.ncbi.nlm.nih.gov/pubmed/27311887
http://dx.doi.org/10.1186/s12862-016-0699-8
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