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Diminishing-returns epistasis among random beneficial mutations in a multicellular fungus
Adaptive evolution ultimately is fuelled by mutations generating novel genetic variation. Non-additivity of fitness effects of mutations (called epistasis) may affect the dynamics and repeatability of adaptation. However, understanding the importance and implications of epistasis is hampered by the...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5013798/ https://www.ncbi.nlm.nih.gov/pubmed/27559062 http://dx.doi.org/10.1098/rspb.2016.1376 |
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author | Schoustra, Sijmen Hwang, Sungmin Krug, Joachim de Visser, J. Arjan G. M. |
author_facet | Schoustra, Sijmen Hwang, Sungmin Krug, Joachim de Visser, J. Arjan G. M. |
author_sort | Schoustra, Sijmen |
collection | PubMed |
description | Adaptive evolution ultimately is fuelled by mutations generating novel genetic variation. Non-additivity of fitness effects of mutations (called epistasis) may affect the dynamics and repeatability of adaptation. However, understanding the importance and implications of epistasis is hampered by the observation of substantial variation in patterns of epistasis across empirical studies. Interestingly, some recent studies report increasingly smaller benefits of beneficial mutations once genotypes become better adapted (called diminishing-returns epistasis) in unicellular microbes and single genes. Here, we use Fisher's geometric model (FGM) to generate analytical predictions about the relationship between the effect size of mutations and the extent of epistasis. We then test these predictions using the multicellular fungus Aspergillus nidulans by generating a collection of 108 strains in either a poor or a rich nutrient environment that each carry a beneficial mutation and constructing pairwise combinations using sexual crosses. Our results support the predictions from FGM and indicate negative epistasis among beneficial mutations in both environments, which scale with mutational effect size. Hence, our findings show the importance of diminishing-returns epistasis among beneficial mutations also for a multicellular organism, and suggest that this pattern reflects a generic constraint operating at diverse levels of biological organization. |
format | Online Article Text |
id | pubmed-5013798 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-50137982016-10-04 Diminishing-returns epistasis among random beneficial mutations in a multicellular fungus Schoustra, Sijmen Hwang, Sungmin Krug, Joachim de Visser, J. Arjan G. M. Proc Biol Sci Research Articles Adaptive evolution ultimately is fuelled by mutations generating novel genetic variation. Non-additivity of fitness effects of mutations (called epistasis) may affect the dynamics and repeatability of adaptation. However, understanding the importance and implications of epistasis is hampered by the observation of substantial variation in patterns of epistasis across empirical studies. Interestingly, some recent studies report increasingly smaller benefits of beneficial mutations once genotypes become better adapted (called diminishing-returns epistasis) in unicellular microbes and single genes. Here, we use Fisher's geometric model (FGM) to generate analytical predictions about the relationship between the effect size of mutations and the extent of epistasis. We then test these predictions using the multicellular fungus Aspergillus nidulans by generating a collection of 108 strains in either a poor or a rich nutrient environment that each carry a beneficial mutation and constructing pairwise combinations using sexual crosses. Our results support the predictions from FGM and indicate negative epistasis among beneficial mutations in both environments, which scale with mutational effect size. Hence, our findings show the importance of diminishing-returns epistasis among beneficial mutations also for a multicellular organism, and suggest that this pattern reflects a generic constraint operating at diverse levels of biological organization. The Royal Society 2016-08-31 /pmc/articles/PMC5013798/ /pubmed/27559062 http://dx.doi.org/10.1098/rspb.2016.1376 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 | Research Articles Schoustra, Sijmen Hwang, Sungmin Krug, Joachim de Visser, J. Arjan G. M. Diminishing-returns epistasis among random beneficial mutations in a multicellular fungus |
title | Diminishing-returns epistasis among random beneficial mutations in a multicellular fungus |
title_full | Diminishing-returns epistasis among random beneficial mutations in a multicellular fungus |
title_fullStr | Diminishing-returns epistasis among random beneficial mutations in a multicellular fungus |
title_full_unstemmed | Diminishing-returns epistasis among random beneficial mutations in a multicellular fungus |
title_short | Diminishing-returns epistasis among random beneficial mutations in a multicellular fungus |
title_sort | diminishing-returns epistasis among random beneficial mutations in a multicellular fungus |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5013798/ https://www.ncbi.nlm.nih.gov/pubmed/27559062 http://dx.doi.org/10.1098/rspb.2016.1376 |
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