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Survival of the simplest in microbial evolution

The evolution of microbial and viral organisms often generates clonal interference, a mode of competition between genetic clades within a population. Here we show how interference impacts systems biology by constraining genetic and phenotypic complexity. Our analysis uses biophysically grounded evol...

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Detalles Bibliográficos
Autores principales: Held, Torsten, Klemmer, Daniel, Lässig, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6554311/
https://www.ncbi.nlm.nih.gov/pubmed/31171781
http://dx.doi.org/10.1038/s41467-019-10413-8
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author Held, Torsten
Klemmer, Daniel
Lässig, Michael
author_facet Held, Torsten
Klemmer, Daniel
Lässig, Michael
author_sort Held, Torsten
collection PubMed
description The evolution of microbial and viral organisms often generates clonal interference, a mode of competition between genetic clades within a population. Here we show how interference impacts systems biology by constraining genetic and phenotypic complexity. Our analysis uses biophysically grounded evolutionary models for molecular phenotypes, such as fold stability and enzymatic activity of genes. We find a generic mode of phenotypic interference that couples the function of individual genes and the population’s global evolutionary dynamics. Biological implications of phenotypic interference include rapid collateral system degradation in adaptation experiments and long-term selection against genome complexity: each additional gene carries a cost proportional to the total number of genes. Recombination above a threshold rate can eliminate this cost, which establishes a universal, biophysically grounded scenario for the evolution of sex. In a broader context, our analysis suggests that the systems biology of microbes is strongly intertwined with their mode of evolution.
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spelling pubmed-65543112019-06-17 Survival of the simplest in microbial evolution Held, Torsten Klemmer, Daniel Lässig, Michael Nat Commun Article The evolution of microbial and viral organisms often generates clonal interference, a mode of competition between genetic clades within a population. Here we show how interference impacts systems biology by constraining genetic and phenotypic complexity. Our analysis uses biophysically grounded evolutionary models for molecular phenotypes, such as fold stability and enzymatic activity of genes. We find a generic mode of phenotypic interference that couples the function of individual genes and the population’s global evolutionary dynamics. Biological implications of phenotypic interference include rapid collateral system degradation in adaptation experiments and long-term selection against genome complexity: each additional gene carries a cost proportional to the total number of genes. Recombination above a threshold rate can eliminate this cost, which establishes a universal, biophysically grounded scenario for the evolution of sex. In a broader context, our analysis suggests that the systems biology of microbes is strongly intertwined with their mode of evolution. Nature Publishing Group UK 2019-06-06 /pmc/articles/PMC6554311/ /pubmed/31171781 http://dx.doi.org/10.1038/s41467-019-10413-8 Text en © The Author(s) 2019 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
Held, Torsten
Klemmer, Daniel
Lässig, Michael
Survival of the simplest in microbial evolution
title Survival of the simplest in microbial evolution
title_full Survival of the simplest in microbial evolution
title_fullStr Survival of the simplest in microbial evolution
title_full_unstemmed Survival of the simplest in microbial evolution
title_short Survival of the simplest in microbial evolution
title_sort survival of the simplest in microbial evolution
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6554311/
https://www.ncbi.nlm.nih.gov/pubmed/31171781
http://dx.doi.org/10.1038/s41467-019-10413-8
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