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Pervasive function and evidence for selection across standing genetic variation in S. cerevisiae
Quantitative genetics aims to map genotype to phenotype, often with the goal of understanding how organisms evolved. However, it remains unclear whether the genetic variants identified are exemplary of evolution. Here we analyzed progeny of two wild Saccharomyces cerevisiae isolates to identify 195...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6420628/ https://www.ncbi.nlm.nih.gov/pubmed/30874558 http://dx.doi.org/10.1038/s41467-019-09166-1 |
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author | Jakobson, Christopher M. She, Richard Jarosz, Daniel F. |
author_facet | Jakobson, Christopher M. She, Richard Jarosz, Daniel F. |
author_sort | Jakobson, Christopher M. |
collection | PubMed |
description | Quantitative genetics aims to map genotype to phenotype, often with the goal of understanding how organisms evolved. However, it remains unclear whether the genetic variants identified are exemplary of evolution. Here we analyzed progeny of two wild Saccharomyces cerevisiae isolates to identify 195 loci underlying complex metabolic traits, resolving 107 to single polymorphisms with diverse molecular mechanisms. More than 20% of causal variants exhibited patterns of emergence inconsistent with neutrality. Moreover, contrary to drift-centric expectation, variation in diverse wild yeast isolates broadly exhibited this property: over 30% of shared natural variants exhibited phylogenetic signatures suggesting that they are not neutral. This pattern is likely attributable to both homoplasy and balancing selection on ancestral polymorphism. Variants that emerged repeatedly were more likely to have done so in isolates from the same ecological niche. Our results underscore the power of super-resolution mapping of ecologically relevant traits in understanding adaptation and evolution. |
format | Online Article Text |
id | pubmed-6420628 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64206282019-03-18 Pervasive function and evidence for selection across standing genetic variation in S. cerevisiae Jakobson, Christopher M. She, Richard Jarosz, Daniel F. Nat Commun Article Quantitative genetics aims to map genotype to phenotype, often with the goal of understanding how organisms evolved. However, it remains unclear whether the genetic variants identified are exemplary of evolution. Here we analyzed progeny of two wild Saccharomyces cerevisiae isolates to identify 195 loci underlying complex metabolic traits, resolving 107 to single polymorphisms with diverse molecular mechanisms. More than 20% of causal variants exhibited patterns of emergence inconsistent with neutrality. Moreover, contrary to drift-centric expectation, variation in diverse wild yeast isolates broadly exhibited this property: over 30% of shared natural variants exhibited phylogenetic signatures suggesting that they are not neutral. This pattern is likely attributable to both homoplasy and balancing selection on ancestral polymorphism. Variants that emerged repeatedly were more likely to have done so in isolates from the same ecological niche. Our results underscore the power of super-resolution mapping of ecologically relevant traits in understanding adaptation and evolution. Nature Publishing Group UK 2019-03-15 /pmc/articles/PMC6420628/ /pubmed/30874558 http://dx.doi.org/10.1038/s41467-019-09166-1 Text en © The Author(s) 2019 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/. |
spellingShingle | Article Jakobson, Christopher M. She, Richard Jarosz, Daniel F. Pervasive function and evidence for selection across standing genetic variation in S. cerevisiae |
title | Pervasive function and evidence for selection across standing genetic variation in S. cerevisiae |
title_full | Pervasive function and evidence for selection across standing genetic variation in S. cerevisiae |
title_fullStr | Pervasive function and evidence for selection across standing genetic variation in S. cerevisiae |
title_full_unstemmed | Pervasive function and evidence for selection across standing genetic variation in S. cerevisiae |
title_short | Pervasive function and evidence for selection across standing genetic variation in S. cerevisiae |
title_sort | pervasive function and evidence for selection across standing genetic variation in s. cerevisiae |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6420628/ https://www.ncbi.nlm.nih.gov/pubmed/30874558 http://dx.doi.org/10.1038/s41467-019-09166-1 |
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