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Genome-wide signatures of synergistic epistasis during parallel adaptation in a Baltic Sea copepod
The role of epistasis in driving adaptation has remained an unresolved problem dating back to the Evolutionary Synthesis. In particular, whether epistatic interactions among genes could promote parallel evolution remains unexplored. To address this problem, we employ an Evolve and Resequence (E&...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9276764/ https://www.ncbi.nlm.nih.gov/pubmed/35821220 http://dx.doi.org/10.1038/s41467-022-31622-8 |
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author | Stern, David B. Anderson, Nathan W. Diaz, Juanita A. Lee, Carol Eunmi |
author_facet | Stern, David B. Anderson, Nathan W. Diaz, Juanita A. Lee, Carol Eunmi |
author_sort | Stern, David B. |
collection | PubMed |
description | The role of epistasis in driving adaptation has remained an unresolved problem dating back to the Evolutionary Synthesis. In particular, whether epistatic interactions among genes could promote parallel evolution remains unexplored. To address this problem, we employ an Evolve and Resequence (E&R) experiment, using the copepod Eurytemora affinis, to elucidate the evolutionary genomic response to rapid salinity decline. Rapid declines in coastal salinity at high latitudes are a predicted consequence of global climate change. Based on time-resolved pooled whole-genome sequencing, we uncover a remarkably parallel, polygenic response across ten replicate selection lines, with 79.4% of selected alleles shared between lines by the tenth generation of natural selection. Using extensive computer simulations of our experiment conditions, we find that this polygenic parallelism is consistent with positive synergistic epistasis among alleles, far more so than other mechanisms tested. Our study provides experimental and theoretical support for a novel mechanism promoting repeatable polygenic adaptation, a phenomenon that may be common for selection on complex physiological traits. |
format | Online Article Text |
id | pubmed-9276764 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-92767642022-07-14 Genome-wide signatures of synergistic epistasis during parallel adaptation in a Baltic Sea copepod Stern, David B. Anderson, Nathan W. Diaz, Juanita A. Lee, Carol Eunmi Nat Commun Article The role of epistasis in driving adaptation has remained an unresolved problem dating back to the Evolutionary Synthesis. In particular, whether epistatic interactions among genes could promote parallel evolution remains unexplored. To address this problem, we employ an Evolve and Resequence (E&R) experiment, using the copepod Eurytemora affinis, to elucidate the evolutionary genomic response to rapid salinity decline. Rapid declines in coastal salinity at high latitudes are a predicted consequence of global climate change. Based on time-resolved pooled whole-genome sequencing, we uncover a remarkably parallel, polygenic response across ten replicate selection lines, with 79.4% of selected alleles shared between lines by the tenth generation of natural selection. Using extensive computer simulations of our experiment conditions, we find that this polygenic parallelism is consistent with positive synergistic epistasis among alleles, far more so than other mechanisms tested. Our study provides experimental and theoretical support for a novel mechanism promoting repeatable polygenic adaptation, a phenomenon that may be common for selection on complex physiological traits. Nature Publishing Group UK 2022-07-12 /pmc/articles/PMC9276764/ /pubmed/35821220 http://dx.doi.org/10.1038/s41467-022-31622-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Stern, David B. Anderson, Nathan W. Diaz, Juanita A. Lee, Carol Eunmi Genome-wide signatures of synergistic epistasis during parallel adaptation in a Baltic Sea copepod |
title | Genome-wide signatures of synergistic epistasis during parallel adaptation in a Baltic Sea copepod |
title_full | Genome-wide signatures of synergistic epistasis during parallel adaptation in a Baltic Sea copepod |
title_fullStr | Genome-wide signatures of synergistic epistasis during parallel adaptation in a Baltic Sea copepod |
title_full_unstemmed | Genome-wide signatures of synergistic epistasis during parallel adaptation in a Baltic Sea copepod |
title_short | Genome-wide signatures of synergistic epistasis during parallel adaptation in a Baltic Sea copepod |
title_sort | genome-wide signatures of synergistic epistasis during parallel adaptation in a baltic sea copepod |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9276764/ https://www.ncbi.nlm.nih.gov/pubmed/35821220 http://dx.doi.org/10.1038/s41467-022-31622-8 |
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