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The Local Coexistence Pattern of Selfing Genotypes in Caenorhabditis elegans Natural Metapopulations

To study the interplay of rare outcrossing and metapopulation structure, we focus on the nematode Caenorhabditis elegans. Its remarkably low outcrossing rate is at the extreme end of the spectrum for facultative selfing organisms. At the demographic level, C. elegans natural populations undergo boom...

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Autores principales: Richaud, Aurélien, Zhang, Gaotian, Lee, Daehan, Lee, Junho, Félix, Marie-Anne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5788539/
https://www.ncbi.nlm.nih.gov/pubmed/29242287
http://dx.doi.org/10.1534/genetics.117.300564
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author Richaud, Aurélien
Zhang, Gaotian
Lee, Daehan
Lee, Junho
Félix, Marie-Anne
author_facet Richaud, Aurélien
Zhang, Gaotian
Lee, Daehan
Lee, Junho
Félix, Marie-Anne
author_sort Richaud, Aurélien
collection PubMed
description To study the interplay of rare outcrossing and metapopulation structure, we focus on the nematode Caenorhabditis elegans. Its remarkably low outcrossing rate is at the extreme end of the spectrum for facultative selfing organisms. At the demographic level, C. elegans natural populations undergo boom and bust dynamics on ephemeral resources, with the dauer diapause larva acting as the dispersal form. Here we investigate the small-scale genetic structure of C. elegans populations in two localities over several years, using 2b restriction-associated DNA sequencing of nearly 1000 individuals. We find a remarkably small number of genome-wide haplotypes, almost exclusively in the homozygous state, confirming the low effective outcrossing rate. Most strikingly, the major haplotypes in a locality remain intact and do not effectively recombine over several years. From the spatial pattern of diversity, we estimate that each subpopulation or deme is seeded by a mean of 3–10 immigrating individuals. Populations are thus formed by clones that compete at two levels, within a subpopulation and at the metapopulation level. We test for the presence of local phenotypic variation in pathogen resistance and dauer larva nictation, which could possibly explain the maintenance of different genotypes by heterogeneous selection in different local environments or lifecycles. This study is the first to address the local spatiotemporal genetic structure of C. elegans on feeding substrates. We conclude that these animals coexist as competing homozygous clones at the smallest population scale as well as in the metapopulation.
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spelling pubmed-57885392018-01-30 The Local Coexistence Pattern of Selfing Genotypes in Caenorhabditis elegans Natural Metapopulations Richaud, Aurélien Zhang, Gaotian Lee, Daehan Lee, Junho Félix, Marie-Anne Genetics Investigations To study the interplay of rare outcrossing and metapopulation structure, we focus on the nematode Caenorhabditis elegans. Its remarkably low outcrossing rate is at the extreme end of the spectrum for facultative selfing organisms. At the demographic level, C. elegans natural populations undergo boom and bust dynamics on ephemeral resources, with the dauer diapause larva acting as the dispersal form. Here we investigate the small-scale genetic structure of C. elegans populations in two localities over several years, using 2b restriction-associated DNA sequencing of nearly 1000 individuals. We find a remarkably small number of genome-wide haplotypes, almost exclusively in the homozygous state, confirming the low effective outcrossing rate. Most strikingly, the major haplotypes in a locality remain intact and do not effectively recombine over several years. From the spatial pattern of diversity, we estimate that each subpopulation or deme is seeded by a mean of 3–10 immigrating individuals. Populations are thus formed by clones that compete at two levels, within a subpopulation and at the metapopulation level. We test for the presence of local phenotypic variation in pathogen resistance and dauer larva nictation, which could possibly explain the maintenance of different genotypes by heterogeneous selection in different local environments or lifecycles. This study is the first to address the local spatiotemporal genetic structure of C. elegans on feeding substrates. We conclude that these animals coexist as competing homozygous clones at the smallest population scale as well as in the metapopulation. Genetics Society of America 2018-02 2017-12-12 /pmc/articles/PMC5788539/ /pubmed/29242287 http://dx.doi.org/10.1534/genetics.117.300564 Text en Copyright © 2018 Richaud et al. Available freely online through the author-supported open access option. This is an open-access article 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 the original work is properly cited.
spellingShingle Investigations
Richaud, Aurélien
Zhang, Gaotian
Lee, Daehan
Lee, Junho
Félix, Marie-Anne
The Local Coexistence Pattern of Selfing Genotypes in Caenorhabditis elegans Natural Metapopulations
title The Local Coexistence Pattern of Selfing Genotypes in Caenorhabditis elegans Natural Metapopulations
title_full The Local Coexistence Pattern of Selfing Genotypes in Caenorhabditis elegans Natural Metapopulations
title_fullStr The Local Coexistence Pattern of Selfing Genotypes in Caenorhabditis elegans Natural Metapopulations
title_full_unstemmed The Local Coexistence Pattern of Selfing Genotypes in Caenorhabditis elegans Natural Metapopulations
title_short The Local Coexistence Pattern of Selfing Genotypes in Caenorhabditis elegans Natural Metapopulations
title_sort local coexistence pattern of selfing genotypes in caenorhabditis elegans natural metapopulations
topic Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5788539/
https://www.ncbi.nlm.nih.gov/pubmed/29242287
http://dx.doi.org/10.1534/genetics.117.300564
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