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Insertion-sequence-mediated mutations both promote and constrain evolvability during a long-term experiment with bacteria
Insertion sequences (IS) are ubiquitous bacterial mobile genetic elements, and the mutations they cause can be deleterious, neutral, or beneficial. The long-term dynamics of IS elements and their effects on bacteria are poorly understood, including whether they are primarily genomic parasites or imp...
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/PMC7881107/ https://www.ncbi.nlm.nih.gov/pubmed/33579917 http://dx.doi.org/10.1038/s41467-021-21210-7 |
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author | Consuegra, Jessika Gaffé, Joël Lenski, Richard E. Hindré, Thomas Barrick, Jeffrey E. Tenaillon, Olivier Schneider, Dominique |
author_facet | Consuegra, Jessika Gaffé, Joël Lenski, Richard E. Hindré, Thomas Barrick, Jeffrey E. Tenaillon, Olivier Schneider, Dominique |
author_sort | Consuegra, Jessika |
collection | PubMed |
description | Insertion sequences (IS) are ubiquitous bacterial mobile genetic elements, and the mutations they cause can be deleterious, neutral, or beneficial. The long-term dynamics of IS elements and their effects on bacteria are poorly understood, including whether they are primarily genomic parasites or important drivers of adaptation by natural selection. Here, we investigate the dynamics of IS elements and their contribution to genomic evolution and fitness during a long-term experiment with Escherichia coli. IS elements account for ~35% of the mutations that reached high frequency through 50,000 generations in those populations that retained the ancestral point-mutation rate. In mutator populations, IS-mediated mutations are only half as frequent in absolute numbers. In one population, an exceptionally high ~8-fold increase in IS150 copy number is associated with the beneficial effects of early insertion mutations; however, this expansion later slowed down owing to reduced IS150 activity. This population also achieves the lowest fitness, suggesting that some avenues for further adaptation are precluded by the IS150-mediated mutations. More generally, across all populations, we find that higher IS activity becomes detrimental to adaptation over evolutionary time. Therefore, IS-mediated mutations can both promote and constrain evolvability. |
format | Online Article Text |
id | pubmed-7881107 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78811072021-02-24 Insertion-sequence-mediated mutations both promote and constrain evolvability during a long-term experiment with bacteria Consuegra, Jessika Gaffé, Joël Lenski, Richard E. Hindré, Thomas Barrick, Jeffrey E. Tenaillon, Olivier Schneider, Dominique Nat Commun Article Insertion sequences (IS) are ubiquitous bacterial mobile genetic elements, and the mutations they cause can be deleterious, neutral, or beneficial. The long-term dynamics of IS elements and their effects on bacteria are poorly understood, including whether they are primarily genomic parasites or important drivers of adaptation by natural selection. Here, we investigate the dynamics of IS elements and their contribution to genomic evolution and fitness during a long-term experiment with Escherichia coli. IS elements account for ~35% of the mutations that reached high frequency through 50,000 generations in those populations that retained the ancestral point-mutation rate. In mutator populations, IS-mediated mutations are only half as frequent in absolute numbers. In one population, an exceptionally high ~8-fold increase in IS150 copy number is associated with the beneficial effects of early insertion mutations; however, this expansion later slowed down owing to reduced IS150 activity. This population also achieves the lowest fitness, suggesting that some avenues for further adaptation are precluded by the IS150-mediated mutations. More generally, across all populations, we find that higher IS activity becomes detrimental to adaptation over evolutionary time. Therefore, IS-mediated mutations can both promote and constrain evolvability. Nature Publishing Group UK 2021-02-12 /pmc/articles/PMC7881107/ /pubmed/33579917 http://dx.doi.org/10.1038/s41467-021-21210-7 Text en © The Author(s) 2021 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/. |
spellingShingle | Article Consuegra, Jessika Gaffé, Joël Lenski, Richard E. Hindré, Thomas Barrick, Jeffrey E. Tenaillon, Olivier Schneider, Dominique Insertion-sequence-mediated mutations both promote and constrain evolvability during a long-term experiment with bacteria |
title | Insertion-sequence-mediated mutations both promote and constrain evolvability during a long-term experiment with bacteria |
title_full | Insertion-sequence-mediated mutations both promote and constrain evolvability during a long-term experiment with bacteria |
title_fullStr | Insertion-sequence-mediated mutations both promote and constrain evolvability during a long-term experiment with bacteria |
title_full_unstemmed | Insertion-sequence-mediated mutations both promote and constrain evolvability during a long-term experiment with bacteria |
title_short | Insertion-sequence-mediated mutations both promote and constrain evolvability during a long-term experiment with bacteria |
title_sort | insertion-sequence-mediated mutations both promote and constrain evolvability during a long-term experiment with bacteria |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7881107/ https://www.ncbi.nlm.nih.gov/pubmed/33579917 http://dx.doi.org/10.1038/s41467-021-21210-7 |
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