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Evolution in eggs and phases: experimental evolution of fecundity and reproductive timing in Caenorhabditis elegans

To examine the role of natural selection in fecundity in a variety of Caenorhabditis elegans genetic backgrounds, we used an experimental evolution protocol to evolve 14 distinct genetic strains over 15–20 generations. We were able to generate 790 distinct genealogies, which provided information on...

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Autor principal: Alicea, Bradly
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5180133/
https://www.ncbi.nlm.nih.gov/pubmed/28018635
http://dx.doi.org/10.1098/rsos.160496
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author Alicea, Bradly
author_facet Alicea, Bradly
author_sort Alicea, Bradly
collection PubMed
description To examine the role of natural selection in fecundity in a variety of Caenorhabditis elegans genetic backgrounds, we used an experimental evolution protocol to evolve 14 distinct genetic strains over 15–20 generations. We were able to generate 790 distinct genealogies, which provided information on both the effects of natural selection and the evolvability of each strain. Among these genotypes are a wild-type (N2) and a collection of mutants with targeted mutations in the daf-c, daf-d and AMPK pathways. Differences are observed in reproductive fitness along with related changes in reproductive timing. The majority of selective effects on fecundity occur during the first few generations of evolution, while the negative selection for reproductive timing occurs on longer time scales. In addition, positive selection on fecundity results in positive and negative strain-dependent selection on reproductive timing. A derivative of population size per generation called reproductive carry-over (RCO) may be informative in terms of developmental selection. While these findings transcend mutations in a specific gene, changes in the RCO measure may nevertheless be products of selection. In conclusion, the broader implications of these findings are discussed, particularly in the context of genotype-fitness maps and the role of uncharacterized mutations in individual variation and evolvability.
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spelling pubmed-51801332016-12-23 Evolution in eggs and phases: experimental evolution of fecundity and reproductive timing in Caenorhabditis elegans Alicea, Bradly R Soc Open Sci Biology (Whole Organism) To examine the role of natural selection in fecundity in a variety of Caenorhabditis elegans genetic backgrounds, we used an experimental evolution protocol to evolve 14 distinct genetic strains over 15–20 generations. We were able to generate 790 distinct genealogies, which provided information on both the effects of natural selection and the evolvability of each strain. Among these genotypes are a wild-type (N2) and a collection of mutants with targeted mutations in the daf-c, daf-d and AMPK pathways. Differences are observed in reproductive fitness along with related changes in reproductive timing. The majority of selective effects on fecundity occur during the first few generations of evolution, while the negative selection for reproductive timing occurs on longer time scales. In addition, positive selection on fecundity results in positive and negative strain-dependent selection on reproductive timing. A derivative of population size per generation called reproductive carry-over (RCO) may be informative in terms of developmental selection. While these findings transcend mutations in a specific gene, changes in the RCO measure may nevertheless be products of selection. In conclusion, the broader implications of these findings are discussed, particularly in the context of genotype-fitness maps and the role of uncharacterized mutations in individual variation and evolvability. The Royal Society 2016-11-09 /pmc/articles/PMC5180133/ /pubmed/28018635 http://dx.doi.org/10.1098/rsos.160496 Text en © 2016 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 Biology (Whole Organism)
Alicea, Bradly
Evolution in eggs and phases: experimental evolution of fecundity and reproductive timing in Caenorhabditis elegans
title Evolution in eggs and phases: experimental evolution of fecundity and reproductive timing in Caenorhabditis elegans
title_full Evolution in eggs and phases: experimental evolution of fecundity and reproductive timing in Caenorhabditis elegans
title_fullStr Evolution in eggs and phases: experimental evolution of fecundity and reproductive timing in Caenorhabditis elegans
title_full_unstemmed Evolution in eggs and phases: experimental evolution of fecundity and reproductive timing in Caenorhabditis elegans
title_short Evolution in eggs and phases: experimental evolution of fecundity and reproductive timing in Caenorhabditis elegans
title_sort evolution in eggs and phases: experimental evolution of fecundity and reproductive timing in caenorhabditis elegans
topic Biology (Whole Organism)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5180133/
https://www.ncbi.nlm.nih.gov/pubmed/28018635
http://dx.doi.org/10.1098/rsos.160496
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