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Long-Term m5C Methylome Dynamics Parallel Phenotypic Adaptation in the Cyanobacterium Trichodesmium
A major challenge in modern biology is understanding how the effects of short-term biological responses influence long-term evolutionary adaptation, defined as a genetically determined increase in fitness to novel environments. This is particularly important in globally important microbes experienci...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7947765/ https://www.ncbi.nlm.nih.gov/pubmed/33022053 http://dx.doi.org/10.1093/molbev/msaa256 |
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author | Walworth, Nathan G Lee, Michael D Dolzhenko, Egor Fu, Fei-Xue Smith, Andrew D Webb, Eric A Hutchins, David A |
author_facet | Walworth, Nathan G Lee, Michael D Dolzhenko, Egor Fu, Fei-Xue Smith, Andrew D Webb, Eric A Hutchins, David A |
author_sort | Walworth, Nathan G |
collection | PubMed |
description | A major challenge in modern biology is understanding how the effects of short-term biological responses influence long-term evolutionary adaptation, defined as a genetically determined increase in fitness to novel environments. This is particularly important in globally important microbes experiencing rapid global change, due to their influence on food webs, biogeochemical cycles, and climate. Epigenetic modifications like methylation have been demonstrated to influence short-term plastic responses, which ultimately impact long-term adaptive responses to environmental change. However, there remains a paucity of empirical research examining long-term methylation dynamics during environmental adaptation in nonmodel, ecologically important microbes. Here, we show the first empirical evidence in a marine prokaryote for long-term m5C methylome modifications correlated with phenotypic adaptation to CO(2), using a 7-year evolution experiment (1,000+ generations) with the biogeochemically important marine cyanobacterium Trichodesmium. We identify m5C methylated sites that rapidly changed in response to high (750 µatm) CO(2) exposure and were maintained for at least 4.5 years of CO(2) selection. After 7 years of CO(2) selection, however, m5C methylation levels that initially responded to high-CO(2) returned to ancestral, ambient CO(2) levels. Concurrently, high-CO(2) adapted growth and N(2) fixation rates remained significantly higher than those of ambient CO(2) adapted cell lines irrespective of CO(2) concentration, a trend consistent with genetic assimilation theory. These data demonstrate the maintenance of CO(2)-responsive m5C methylation for 4.5 years alongside phenotypic adaptation before returning to ancestral methylation levels. These observations in a globally distributed marine prokaryote provide critical evolutionary insights into biogeochemically important traits under global change. |
format | Online Article Text |
id | pubmed-7947765 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-79477652021-03-16 Long-Term m5C Methylome Dynamics Parallel Phenotypic Adaptation in the Cyanobacterium Trichodesmium Walworth, Nathan G Lee, Michael D Dolzhenko, Egor Fu, Fei-Xue Smith, Andrew D Webb, Eric A Hutchins, David A Mol Biol Evol Discoveries A major challenge in modern biology is understanding how the effects of short-term biological responses influence long-term evolutionary adaptation, defined as a genetically determined increase in fitness to novel environments. This is particularly important in globally important microbes experiencing rapid global change, due to their influence on food webs, biogeochemical cycles, and climate. Epigenetic modifications like methylation have been demonstrated to influence short-term plastic responses, which ultimately impact long-term adaptive responses to environmental change. However, there remains a paucity of empirical research examining long-term methylation dynamics during environmental adaptation in nonmodel, ecologically important microbes. Here, we show the first empirical evidence in a marine prokaryote for long-term m5C methylome modifications correlated with phenotypic adaptation to CO(2), using a 7-year evolution experiment (1,000+ generations) with the biogeochemically important marine cyanobacterium Trichodesmium. We identify m5C methylated sites that rapidly changed in response to high (750 µatm) CO(2) exposure and were maintained for at least 4.5 years of CO(2) selection. After 7 years of CO(2) selection, however, m5C methylation levels that initially responded to high-CO(2) returned to ancestral, ambient CO(2) levels. Concurrently, high-CO(2) adapted growth and N(2) fixation rates remained significantly higher than those of ambient CO(2) adapted cell lines irrespective of CO(2) concentration, a trend consistent with genetic assimilation theory. These data demonstrate the maintenance of CO(2)-responsive m5C methylation for 4.5 years alongside phenotypic adaptation before returning to ancestral methylation levels. These observations in a globally distributed marine prokaryote provide critical evolutionary insights into biogeochemically important traits under global change. Oxford University Press 2020-10-06 /pmc/articles/PMC7947765/ /pubmed/33022053 http://dx.doi.org/10.1093/molbev/msaa256 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Discoveries Walworth, Nathan G Lee, Michael D Dolzhenko, Egor Fu, Fei-Xue Smith, Andrew D Webb, Eric A Hutchins, David A Long-Term m5C Methylome Dynamics Parallel Phenotypic Adaptation in the Cyanobacterium Trichodesmium |
title | Long-Term m5C Methylome Dynamics Parallel Phenotypic Adaptation in the Cyanobacterium Trichodesmium |
title_full | Long-Term m5C Methylome Dynamics Parallel Phenotypic Adaptation in the Cyanobacterium Trichodesmium |
title_fullStr | Long-Term m5C Methylome Dynamics Parallel Phenotypic Adaptation in the Cyanobacterium Trichodesmium |
title_full_unstemmed | Long-Term m5C Methylome Dynamics Parallel Phenotypic Adaptation in the Cyanobacterium Trichodesmium |
title_short | Long-Term m5C Methylome Dynamics Parallel Phenotypic Adaptation in the Cyanobacterium Trichodesmium |
title_sort | long-term m5c methylome dynamics parallel phenotypic adaptation in the cyanobacterium trichodesmium |
topic | Discoveries |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7947765/ https://www.ncbi.nlm.nih.gov/pubmed/33022053 http://dx.doi.org/10.1093/molbev/msaa256 |
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