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Chance and Necessity in the Pleiotropic Consequences of Adaptation for Budding Yeast
Mutations that a population accumulates during evolution in one (“home”) environment may cause fitness gains or losses in other conditions. Such pleiotropic fitness effects determine the evolutionary fate of the population in variable environments and can lead to ecological specialization. It is unc...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8063891/ https://www.ncbi.nlm.nih.gov/pubmed/32152531 http://dx.doi.org/10.1038/s41559-020-1128-3 |
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author | Jerison, Elizabeth R. Ba, Alex N. Nguyen Desai, Michael M. Kryazhimskiy, Sergey |
author_facet | Jerison, Elizabeth R. Ba, Alex N. Nguyen Desai, Michael M. Kryazhimskiy, Sergey |
author_sort | Jerison, Elizabeth R. |
collection | PubMed |
description | Mutations that a population accumulates during evolution in one (“home”) environment may cause fitness gains or losses in other conditions. Such pleiotropic fitness effects determine the evolutionary fate of the population in variable environments and can lead to ecological specialization. It is unclear how the pleiotropic outcomes of evolution are shaped by the intrinsic randomness of the evolutionary process and by the deterministic variation in selection pressures across environments. To address this question, we evolved 20 replicate populations of the yeast Saccharomyces cerevisiae in 11 laboratory environments and measured their fitness across multiple conditions. We found that evolution led to diverse pleiotropic fitness gains and losses, driven by multiple types of mutations. Approximately 60% percent of this variation is explained by a clone’s home environment and the most common parallel genetic changes, while about 40% is attributed to the stochastic accumulation of mutations whose pleiotropic effects are unpredictable. While populations typically specialized to their home environment, generalists also evolved in almost all conditions. Our results suggest that the mutations accumulating during evolution incur a variety of pleiotropic costs and benefits with different probabilities. Therefore, whether a population evolves towards a specialist or a generalist phenotype is heavily influenced by chance. |
format | Online Article Text |
id | pubmed-8063891 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
record_format | MEDLINE/PubMed |
spelling | pubmed-80638912021-04-23 Chance and Necessity in the Pleiotropic Consequences of Adaptation for Budding Yeast Jerison, Elizabeth R. Ba, Alex N. Nguyen Desai, Michael M. Kryazhimskiy, Sergey Nat Ecol Evol Article Mutations that a population accumulates during evolution in one (“home”) environment may cause fitness gains or losses in other conditions. Such pleiotropic fitness effects determine the evolutionary fate of the population in variable environments and can lead to ecological specialization. It is unclear how the pleiotropic outcomes of evolution are shaped by the intrinsic randomness of the evolutionary process and by the deterministic variation in selection pressures across environments. To address this question, we evolved 20 replicate populations of the yeast Saccharomyces cerevisiae in 11 laboratory environments and measured their fitness across multiple conditions. We found that evolution led to diverse pleiotropic fitness gains and losses, driven by multiple types of mutations. Approximately 60% percent of this variation is explained by a clone’s home environment and the most common parallel genetic changes, while about 40% is attributed to the stochastic accumulation of mutations whose pleiotropic effects are unpredictable. While populations typically specialized to their home environment, generalists also evolved in almost all conditions. Our results suggest that the mutations accumulating during evolution incur a variety of pleiotropic costs and benefits with different probabilities. Therefore, whether a population evolves towards a specialist or a generalist phenotype is heavily influenced by chance. 2020-03-09 2020-04 /pmc/articles/PMC8063891/ /pubmed/32152531 http://dx.doi.org/10.1038/s41559-020-1128-3 Text en https://www.nature.com/authors/policies/license.html#AAMtermsV1Terms of use and reuse: academic research for non-commercial purposes, see here for full terms. https://www.nature.com/authors/policies/license.html#AAMtermsV1 |
spellingShingle | Article Jerison, Elizabeth R. Ba, Alex N. Nguyen Desai, Michael M. Kryazhimskiy, Sergey Chance and Necessity in the Pleiotropic Consequences of Adaptation for Budding Yeast |
title | Chance and Necessity in the Pleiotropic Consequences of Adaptation for Budding Yeast |
title_full | Chance and Necessity in the Pleiotropic Consequences of Adaptation for Budding Yeast |
title_fullStr | Chance and Necessity in the Pleiotropic Consequences of Adaptation for Budding Yeast |
title_full_unstemmed | Chance and Necessity in the Pleiotropic Consequences of Adaptation for Budding Yeast |
title_short | Chance and Necessity in the Pleiotropic Consequences of Adaptation for Budding Yeast |
title_sort | chance and necessity in the pleiotropic consequences of adaptation for budding yeast |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8063891/ https://www.ncbi.nlm.nih.gov/pubmed/32152531 http://dx.doi.org/10.1038/s41559-020-1128-3 |
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