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From passengers to drivers: Impact of bacterial transposable elements on evolvability
Microbes have several mechanisms that promote evolutionary adaptation in stressful environments. The corresponding molecular pathways promote diversity through modulating rates of recombination, mutation or influence the activity of transposable genetic elements. Recent experimental studies suggest...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Landes Bioscience
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3661142/ https://www.ncbi.nlm.nih.gov/pubmed/23734296 http://dx.doi.org/10.4161/mge.23617 |
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author | Pál, Csaba Papp, Balázs |
author_facet | Pál, Csaba Papp, Balázs |
author_sort | Pál, Csaba |
collection | PubMed |
description | Microbes have several mechanisms that promote evolutionary adaptation in stressful environments. The corresponding molecular pathways promote diversity through modulating rates of recombination, mutation or influence the activity of transposable genetic elements. Recent experimental studies suggest an evolutionary conflict between these mechanisms. Specifically, presence of mismatch repair mutator alleles in a bacterial population dramatically reduced fixation of bacterial insertion sequence elements. When rare, these elements had only a limited impact on adaptive evolution compared with other mutation-generating pathways. IS elements may initially spread like molecular parasites, but once present in many copies in a given genome, they might become generators of novelty during bacterial evolution. |
format | Online Article Text |
id | pubmed-3661142 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Landes Bioscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-36611422013-06-03 From passengers to drivers: Impact of bacterial transposable elements on evolvability Pál, Csaba Papp, Balázs Mob Genet Elements Commentary Microbes have several mechanisms that promote evolutionary adaptation in stressful environments. The corresponding molecular pathways promote diversity through modulating rates of recombination, mutation or influence the activity of transposable genetic elements. Recent experimental studies suggest an evolutionary conflict between these mechanisms. Specifically, presence of mismatch repair mutator alleles in a bacterial population dramatically reduced fixation of bacterial insertion sequence elements. When rare, these elements had only a limited impact on adaptive evolution compared with other mutation-generating pathways. IS elements may initially spread like molecular parasites, but once present in many copies in a given genome, they might become generators of novelty during bacterial evolution. Landes Bioscience 2013-01-01 2013-01-01 /pmc/articles/PMC3661142/ /pubmed/23734296 http://dx.doi.org/10.4161/mge.23617 Text en Copyright © 2013 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited. |
spellingShingle | Commentary Pál, Csaba Papp, Balázs From passengers to drivers: Impact of bacterial transposable elements on evolvability |
title | From passengers to drivers: Impact of bacterial transposable elements on evolvability |
title_full | From passengers to drivers: Impact of bacterial transposable elements on evolvability |
title_fullStr | From passengers to drivers: Impact of bacterial transposable elements on evolvability |
title_full_unstemmed | From passengers to drivers: Impact of bacterial transposable elements on evolvability |
title_short | From passengers to drivers: Impact of bacterial transposable elements on evolvability |
title_sort | from passengers to drivers: impact of bacterial transposable elements on evolvability |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3661142/ https://www.ncbi.nlm.nih.gov/pubmed/23734296 http://dx.doi.org/10.4161/mge.23617 |
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