Cargando…

Hermaphrodite life history and the maintenance of partial selfing in experimental populations of Caenorhabditis elegans

BACKGROUND: Classic population genetics theory predicts that mixed reproductive systems, where self reproduction (selfing) and outcrossing co-exist, should not be as common as they are in nature. One means of reconciling theory with observations is to recognize that sexual conflict between males and...

Descripción completa

Detalles Bibliográficos
Autores principales: Carvalho, Sara, Phillips, Patrick C, Teotónio, Henrique
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4052797/
https://www.ncbi.nlm.nih.gov/pubmed/24891140
http://dx.doi.org/10.1186/1471-2148-14-117
_version_ 1782320291215572992
author Carvalho, Sara
Phillips, Patrick C
Teotónio, Henrique
author_facet Carvalho, Sara
Phillips, Patrick C
Teotónio, Henrique
author_sort Carvalho, Sara
collection PubMed
description BACKGROUND: Classic population genetics theory predicts that mixed reproductive systems, where self reproduction (selfing) and outcrossing co-exist, should not be as common as they are in nature. One means of reconciling theory with observations is to recognize that sexual conflict between males and hermaphrodites and/or constraints in the allocation of resources towards sex functions in hermaphrodites can balance the fitness components of selfing and outcrossing. RESULTS: Using experimental evolution in Caenorhabditis elegans, we test whether the adaptive maintenance of partial selfing is due to sexual conflict and/or to the evolution of sex allocation towards male function in hermaphrodites. For this, we characterized the reproductive schedule and longevity patterns in hermaphrodites under selfing and under outcrossing with naïve males that did not have the opportunity to evolve with them. A shift in reproductive schedule towards earlier reproduction would be indicative of adaptation in our imposed life-cycle, while longevity is expected to evolve as a response to the harm that males impinge on hermaphrodites upon mating. To determine adaptation in the absence of constraints in sex allocation, we also characterized the life history of females that reproduced during experimental evolution through obligate mating with males. As expected with adaptation, we find that after 100 generations of experimental evolution, selfing hermaphrodites and females showed improved reproduction at earlier ages. We did not observe similar reproductive shifts in outcrossed hermaphrodites. We further find increased longevity in outcrossed females after evolution but not in outcrossed hermaphrodites, a result that indicates that sexual conflicts were likely more prevalent under male–female evolution than under male-hermaphrodite evolution. CONCLUSIONS: Taken together, our findings suggest that the adaptive maintenance of partial selfing during C. elegans experimental evolution resulted from the evolution of sex allocation towards male function in hermaphrodites.
format Online
Article
Text
id pubmed-4052797
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-40527972014-06-12 Hermaphrodite life history and the maintenance of partial selfing in experimental populations of Caenorhabditis elegans Carvalho, Sara Phillips, Patrick C Teotónio, Henrique BMC Evol Biol Research Article BACKGROUND: Classic population genetics theory predicts that mixed reproductive systems, where self reproduction (selfing) and outcrossing co-exist, should not be as common as they are in nature. One means of reconciling theory with observations is to recognize that sexual conflict between males and hermaphrodites and/or constraints in the allocation of resources towards sex functions in hermaphrodites can balance the fitness components of selfing and outcrossing. RESULTS: Using experimental evolution in Caenorhabditis elegans, we test whether the adaptive maintenance of partial selfing is due to sexual conflict and/or to the evolution of sex allocation towards male function in hermaphrodites. For this, we characterized the reproductive schedule and longevity patterns in hermaphrodites under selfing and under outcrossing with naïve males that did not have the opportunity to evolve with them. A shift in reproductive schedule towards earlier reproduction would be indicative of adaptation in our imposed life-cycle, while longevity is expected to evolve as a response to the harm that males impinge on hermaphrodites upon mating. To determine adaptation in the absence of constraints in sex allocation, we also characterized the life history of females that reproduced during experimental evolution through obligate mating with males. As expected with adaptation, we find that after 100 generations of experimental evolution, selfing hermaphrodites and females showed improved reproduction at earlier ages. We did not observe similar reproductive shifts in outcrossed hermaphrodites. We further find increased longevity in outcrossed females after evolution but not in outcrossed hermaphrodites, a result that indicates that sexual conflicts were likely more prevalent under male–female evolution than under male-hermaphrodite evolution. CONCLUSIONS: Taken together, our findings suggest that the adaptive maintenance of partial selfing during C. elegans experimental evolution resulted from the evolution of sex allocation towards male function in hermaphrodites. BioMed Central 2014-06-02 /pmc/articles/PMC4052797/ /pubmed/24891140 http://dx.doi.org/10.1186/1471-2148-14-117 Text en Copyright © 2014 Carvalho 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 credited. 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
Carvalho, Sara
Phillips, Patrick C
Teotónio, Henrique
Hermaphrodite life history and the maintenance of partial selfing in experimental populations of Caenorhabditis elegans
title Hermaphrodite life history and the maintenance of partial selfing in experimental populations of Caenorhabditis elegans
title_full Hermaphrodite life history and the maintenance of partial selfing in experimental populations of Caenorhabditis elegans
title_fullStr Hermaphrodite life history and the maintenance of partial selfing in experimental populations of Caenorhabditis elegans
title_full_unstemmed Hermaphrodite life history and the maintenance of partial selfing in experimental populations of Caenorhabditis elegans
title_short Hermaphrodite life history and the maintenance of partial selfing in experimental populations of Caenorhabditis elegans
title_sort hermaphrodite life history and the maintenance of partial selfing in experimental populations of caenorhabditis elegans
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4052797/
https://www.ncbi.nlm.nih.gov/pubmed/24891140
http://dx.doi.org/10.1186/1471-2148-14-117
work_keys_str_mv AT carvalhosara hermaphroditelifehistoryandthemaintenanceofpartialselfinginexperimentalpopulationsofcaenorhabditiselegans
AT phillipspatrickc hermaphroditelifehistoryandthemaintenanceofpartialselfinginexperimentalpopulationsofcaenorhabditiselegans
AT teotoniohenrique hermaphroditelifehistoryandthemaintenanceofpartialselfinginexperimentalpopulationsofcaenorhabditiselegans