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Reproductive assurance drives transitions to self-fertilization in experimental Caenorhabditis elegans

BACKGROUND: Evolutionary transitions from outcrossing between individuals to selfing are partly responsible for the great diversity of animal and plant reproduction systems. The hypothesis of ‘reproductive assurance’ suggests that transitions to selfing occur because selfers that are able to reprodu...

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Autores principales: Theologidis, Ioannis, Chelo, Ivo M, Goy, Christine, Teotónio, Henrique
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4234830/
https://www.ncbi.nlm.nih.gov/pubmed/25369737
http://dx.doi.org/10.1186/s12915-014-0093-1
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author Theologidis, Ioannis
Chelo, Ivo M
Goy, Christine
Teotónio, Henrique
author_facet Theologidis, Ioannis
Chelo, Ivo M
Goy, Christine
Teotónio, Henrique
author_sort Theologidis, Ioannis
collection PubMed
description BACKGROUND: Evolutionary transitions from outcrossing between individuals to selfing are partly responsible for the great diversity of animal and plant reproduction systems. The hypothesis of ‘reproductive assurance’ suggests that transitions to selfing occur because selfers that are able to reproduce on their own ensure the persistence of populations in environments where mates or pollination agents are unavailable. Here we test this hypothesis by performing experimental evolution in Caenorhabditis elegans. RESULTS: We show that self-compatible hermaphrodites provide reproductive assurance to a male-female population facing a novel environment where outcrossing is limiting. Invasions of hermaphrodites in male-female populations, and subsequent experimental evolution in the novel environment, led to successful transitions to selfing and adaptation. Adaptation was not due to the loss of males during transitions, as shown by evolution experiments in exclusively hermaphroditic populations and in male-hermaphrodite populations. Instead, adaptation was due to the displacement of females by hermaphrodites. Genotyping of single-nucleotide polymorphisms further indicated that the observed evolution of selfing rates was not due to selection of standing genetic diversity. Finally, numerical modelling and evolution experiments in male-female populations demonstrate that the improvement of male fitness components may diminish the opportunity for reproductive assurance. CONCLUSIONS: Our findings support the hypothesis that reproductive assurance can drive the transition from outcrossing to selfing, and further suggest that the success of transitions to selfing hinges on adaptation of obligate outcrossing populations to the environment where outcrossing was once a limiting factor. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12915-014-0093-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-42348302014-11-19 Reproductive assurance drives transitions to self-fertilization in experimental Caenorhabditis elegans Theologidis, Ioannis Chelo, Ivo M Goy, Christine Teotónio, Henrique BMC Biol Research Article BACKGROUND: Evolutionary transitions from outcrossing between individuals to selfing are partly responsible for the great diversity of animal and plant reproduction systems. The hypothesis of ‘reproductive assurance’ suggests that transitions to selfing occur because selfers that are able to reproduce on their own ensure the persistence of populations in environments where mates or pollination agents are unavailable. Here we test this hypothesis by performing experimental evolution in Caenorhabditis elegans. RESULTS: We show that self-compatible hermaphrodites provide reproductive assurance to a male-female population facing a novel environment where outcrossing is limiting. Invasions of hermaphrodites in male-female populations, and subsequent experimental evolution in the novel environment, led to successful transitions to selfing and adaptation. Adaptation was not due to the loss of males during transitions, as shown by evolution experiments in exclusively hermaphroditic populations and in male-hermaphrodite populations. Instead, adaptation was due to the displacement of females by hermaphrodites. Genotyping of single-nucleotide polymorphisms further indicated that the observed evolution of selfing rates was not due to selection of standing genetic diversity. Finally, numerical modelling and evolution experiments in male-female populations demonstrate that the improvement of male fitness components may diminish the opportunity for reproductive assurance. CONCLUSIONS: Our findings support the hypothesis that reproductive assurance can drive the transition from outcrossing to selfing, and further suggest that the success of transitions to selfing hinges on adaptation of obligate outcrossing populations to the environment where outcrossing was once a limiting factor. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12915-014-0093-1) contains supplementary material, which is available to authorized users. BioMed Central 2014-11-05 /pmc/articles/PMC4234830/ /pubmed/25369737 http://dx.doi.org/10.1186/s12915-014-0093-1 Text en © Theologidis et al.; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), 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
Theologidis, Ioannis
Chelo, Ivo M
Goy, Christine
Teotónio, Henrique
Reproductive assurance drives transitions to self-fertilization in experimental Caenorhabditis elegans
title Reproductive assurance drives transitions to self-fertilization in experimental Caenorhabditis elegans
title_full Reproductive assurance drives transitions to self-fertilization in experimental Caenorhabditis elegans
title_fullStr Reproductive assurance drives transitions to self-fertilization in experimental Caenorhabditis elegans
title_full_unstemmed Reproductive assurance drives transitions to self-fertilization in experimental Caenorhabditis elegans
title_short Reproductive assurance drives transitions to self-fertilization in experimental Caenorhabditis elegans
title_sort reproductive assurance drives transitions to self-fertilization in experimental caenorhabditis elegans
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4234830/
https://www.ncbi.nlm.nih.gov/pubmed/25369737
http://dx.doi.org/10.1186/s12915-014-0093-1
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