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Phenotypic and molecular evolution across 10,000 generations in laboratory budding yeast populations
Laboratory experimental evolution provides a window into the details of the evolutionary process. To investigate the consequences of long-term adaptation, we evolved 205 Saccharomyces cerevisiae populations (124 haploid and 81 diploid) for ~10,000 generations in three environments. We measured the d...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7815316/ https://www.ncbi.nlm.nih.gov/pubmed/33464204 http://dx.doi.org/10.7554/eLife.63910 |
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author | Johnson, Milo S Gopalakrishnan, Shreyas Goyal, Juhee Dillingham, Megan E Bakerlee, Christopher W Humphrey, Parris T Jagdish, Tanush Jerison, Elizabeth R Kosheleva, Katya Lawrence, Katherine R Min, Jiseon Moulana, Alief Phillips, Angela M Piper, Julia C Purkanti, Ramya Rego-Costa, Artur McDonald, Michael J Nguyen Ba, Alex N Desai, Michael M |
author_facet | Johnson, Milo S Gopalakrishnan, Shreyas Goyal, Juhee Dillingham, Megan E Bakerlee, Christopher W Humphrey, Parris T Jagdish, Tanush Jerison, Elizabeth R Kosheleva, Katya Lawrence, Katherine R Min, Jiseon Moulana, Alief Phillips, Angela M Piper, Julia C Purkanti, Ramya Rego-Costa, Artur McDonald, Michael J Nguyen Ba, Alex N Desai, Michael M |
author_sort | Johnson, Milo S |
collection | PubMed |
description | Laboratory experimental evolution provides a window into the details of the evolutionary process. To investigate the consequences of long-term adaptation, we evolved 205 Saccharomyces cerevisiae populations (124 haploid and 81 diploid) for ~10,000 generations in three environments. We measured the dynamics of fitness changes over time, finding repeatable patterns of declining adaptability. Sequencing revealed that this phenotypic adaptation is coupled with a steady accumulation of mutations, widespread genetic parallelism, and historical contingency. In contrast to long-term evolution in E. coli, we do not observe long-term coexistence or populations with highly elevated mutation rates. We find that evolution in diploid populations involves both fixation of heterozygous mutations and frequent loss-of-heterozygosity events. Together, these results help distinguish aspects of evolutionary dynamics that are likely to be general features of adaptation across many systems from those that are specific to individual organisms and environmental conditions. |
format | Online Article Text |
id | pubmed-7815316 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-78153162021-01-21 Phenotypic and molecular evolution across 10,000 generations in laboratory budding yeast populations Johnson, Milo S Gopalakrishnan, Shreyas Goyal, Juhee Dillingham, Megan E Bakerlee, Christopher W Humphrey, Parris T Jagdish, Tanush Jerison, Elizabeth R Kosheleva, Katya Lawrence, Katherine R Min, Jiseon Moulana, Alief Phillips, Angela M Piper, Julia C Purkanti, Ramya Rego-Costa, Artur McDonald, Michael J Nguyen Ba, Alex N Desai, Michael M eLife Evolutionary Biology Laboratory experimental evolution provides a window into the details of the evolutionary process. To investigate the consequences of long-term adaptation, we evolved 205 Saccharomyces cerevisiae populations (124 haploid and 81 diploid) for ~10,000 generations in three environments. We measured the dynamics of fitness changes over time, finding repeatable patterns of declining adaptability. Sequencing revealed that this phenotypic adaptation is coupled with a steady accumulation of mutations, widespread genetic parallelism, and historical contingency. In contrast to long-term evolution in E. coli, we do not observe long-term coexistence or populations with highly elevated mutation rates. We find that evolution in diploid populations involves both fixation of heterozygous mutations and frequent loss-of-heterozygosity events. Together, these results help distinguish aspects of evolutionary dynamics that are likely to be general features of adaptation across many systems from those that are specific to individual organisms and environmental conditions. eLife Sciences Publications, Ltd 2021-01-19 /pmc/articles/PMC7815316/ /pubmed/33464204 http://dx.doi.org/10.7554/eLife.63910 Text en © 2021, Johnson et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Evolutionary Biology Johnson, Milo S Gopalakrishnan, Shreyas Goyal, Juhee Dillingham, Megan E Bakerlee, Christopher W Humphrey, Parris T Jagdish, Tanush Jerison, Elizabeth R Kosheleva, Katya Lawrence, Katherine R Min, Jiseon Moulana, Alief Phillips, Angela M Piper, Julia C Purkanti, Ramya Rego-Costa, Artur McDonald, Michael J Nguyen Ba, Alex N Desai, Michael M Phenotypic and molecular evolution across 10,000 generations in laboratory budding yeast populations |
title | Phenotypic and molecular evolution across 10,000 generations in laboratory budding yeast populations |
title_full | Phenotypic and molecular evolution across 10,000 generations in laboratory budding yeast populations |
title_fullStr | Phenotypic and molecular evolution across 10,000 generations in laboratory budding yeast populations |
title_full_unstemmed | Phenotypic and molecular evolution across 10,000 generations in laboratory budding yeast populations |
title_short | Phenotypic and molecular evolution across 10,000 generations in laboratory budding yeast populations |
title_sort | phenotypic and molecular evolution across 10,000 generations in laboratory budding yeast populations |
topic | Evolutionary Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7815316/ https://www.ncbi.nlm.nih.gov/pubmed/33464204 http://dx.doi.org/10.7554/eLife.63910 |
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