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A mutational hotspot that determines highly repeatable evolution can be built and broken by silent genetic changes
Mutational hotspots can determine evolutionary outcomes and make evolution repeatable. Hotspots are products of multiple evolutionary forces including mutation rate heterogeneity, but this variable is often hard to identify. In this work, we reveal that a near-deterministic genetic hotspot can be bu...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8526746/ https://www.ncbi.nlm.nih.gov/pubmed/34667151 http://dx.doi.org/10.1038/s41467-021-26286-9 |
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author | Horton, James S. Flanagan, Louise M. Jackson, Robert W. Priest, Nicholas K. Taylor, Tiffany B. |
author_facet | Horton, James S. Flanagan, Louise M. Jackson, Robert W. Priest, Nicholas K. Taylor, Tiffany B. |
author_sort | Horton, James S. |
collection | PubMed |
description | Mutational hotspots can determine evolutionary outcomes and make evolution repeatable. Hotspots are products of multiple evolutionary forces including mutation rate heterogeneity, but this variable is often hard to identify. In this work, we reveal that a near-deterministic genetic hotspot can be built and broken by a handful of silent mutations. We observe this when studying homologous immotile variants of the bacteria Pseudomonas fluorescens, AR2 and Pf0-2x. AR2 resurrects motility through highly repeatable de novo mutation of the same nucleotide in >95% lines in minimal media (ntrB A289C). Pf0-2x, however, evolves via a number of mutations meaning the two strains diverge significantly during adaptation. We determine that this evolutionary disparity is owed to just 6 synonymous variations within the ntrB locus, which we demonstrate by swapping the sites and observing that we are able to both break (>95% to 0%) and build (0% to 80%) a deterministic mutational hotspot. Our work reveals a key role for silent genetic variation in determining adaptive outcomes. |
format | Online Article Text |
id | pubmed-8526746 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-85267462021-11-15 A mutational hotspot that determines highly repeatable evolution can be built and broken by silent genetic changes Horton, James S. Flanagan, Louise M. Jackson, Robert W. Priest, Nicholas K. Taylor, Tiffany B. Nat Commun Article Mutational hotspots can determine evolutionary outcomes and make evolution repeatable. Hotspots are products of multiple evolutionary forces including mutation rate heterogeneity, but this variable is often hard to identify. In this work, we reveal that a near-deterministic genetic hotspot can be built and broken by a handful of silent mutations. We observe this when studying homologous immotile variants of the bacteria Pseudomonas fluorescens, AR2 and Pf0-2x. AR2 resurrects motility through highly repeatable de novo mutation of the same nucleotide in >95% lines in minimal media (ntrB A289C). Pf0-2x, however, evolves via a number of mutations meaning the two strains diverge significantly during adaptation. We determine that this evolutionary disparity is owed to just 6 synonymous variations within the ntrB locus, which we demonstrate by swapping the sites and observing that we are able to both break (>95% to 0%) and build (0% to 80%) a deterministic mutational hotspot. Our work reveals a key role for silent genetic variation in determining adaptive outcomes. Nature Publishing Group UK 2021-10-19 /pmc/articles/PMC8526746/ /pubmed/34667151 http://dx.doi.org/10.1038/s41467-021-26286-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Horton, James S. Flanagan, Louise M. Jackson, Robert W. Priest, Nicholas K. Taylor, Tiffany B. A mutational hotspot that determines highly repeatable evolution can be built and broken by silent genetic changes |
title | A mutational hotspot that determines highly repeatable evolution can be built and broken by silent genetic changes |
title_full | A mutational hotspot that determines highly repeatable evolution can be built and broken by silent genetic changes |
title_fullStr | A mutational hotspot that determines highly repeatable evolution can be built and broken by silent genetic changes |
title_full_unstemmed | A mutational hotspot that determines highly repeatable evolution can be built and broken by silent genetic changes |
title_short | A mutational hotspot that determines highly repeatable evolution can be built and broken by silent genetic changes |
title_sort | mutational hotspot that determines highly repeatable evolution can be built and broken by silent genetic changes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8526746/ https://www.ncbi.nlm.nih.gov/pubmed/34667151 http://dx.doi.org/10.1038/s41467-021-26286-9 |
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