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Evolutionary Remodeling of Bacterial Motility Checkpoint Control
Regulatory networks play a central role in the relationship between genotype and phenotype in all organisms. However, the mechanisms that underpin the evolutionary plasticity of these networks remain poorly understood. Here, we used experimental selection for enhanced bacterial motility in a porous...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5289928/ https://www.ncbi.nlm.nih.gov/pubmed/28122238 http://dx.doi.org/10.1016/j.celrep.2016.12.088 |
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author | Ni, Bin Ghosh, Bhaswar Paldy, Ferencz S. Colin, Remy Heimerl, Thomas Sourjik, Victor |
author_facet | Ni, Bin Ghosh, Bhaswar Paldy, Ferencz S. Colin, Remy Heimerl, Thomas Sourjik, Victor |
author_sort | Ni, Bin |
collection | PubMed |
description | Regulatory networks play a central role in the relationship between genotype and phenotype in all organisms. However, the mechanisms that underpin the evolutionary plasticity of these networks remain poorly understood. Here, we used experimental selection for enhanced bacterial motility in a porous environment to explore the adaptability of one of the most complex networks known in bacteria. We found that the resulting phenotypic changes are mediated by adaptive mutations in several functionally different proteins, including multiple components of the flagellar motor. Nevertheless, this evolutionary adaptation could be explained by a single mechanism, namely remodeling of the checkpoint regulating flagellar gene expression. Supported by computer simulations, our findings suggest that the specific “bow-tie” topology of the checkpoint facilitates evolutionary tuning of the cost-benefit trade-off between motility and growth. We propose that bow-tie regulatory motifs, which are widespread in cellular networks, play a general role in evolutionary adaptation. |
format | Online Article Text |
id | pubmed-5289928 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-52899282017-02-13 Evolutionary Remodeling of Bacterial Motility Checkpoint Control Ni, Bin Ghosh, Bhaswar Paldy, Ferencz S. Colin, Remy Heimerl, Thomas Sourjik, Victor Cell Rep Article Regulatory networks play a central role in the relationship between genotype and phenotype in all organisms. However, the mechanisms that underpin the evolutionary plasticity of these networks remain poorly understood. Here, we used experimental selection for enhanced bacterial motility in a porous environment to explore the adaptability of one of the most complex networks known in bacteria. We found that the resulting phenotypic changes are mediated by adaptive mutations in several functionally different proteins, including multiple components of the flagellar motor. Nevertheless, this evolutionary adaptation could be explained by a single mechanism, namely remodeling of the checkpoint regulating flagellar gene expression. Supported by computer simulations, our findings suggest that the specific “bow-tie” topology of the checkpoint facilitates evolutionary tuning of the cost-benefit trade-off between motility and growth. We propose that bow-tie regulatory motifs, which are widespread in cellular networks, play a general role in evolutionary adaptation. Cell Press 2017-01-24 /pmc/articles/PMC5289928/ /pubmed/28122238 http://dx.doi.org/10.1016/j.celrep.2016.12.088 Text en © 2017 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Ni, Bin Ghosh, Bhaswar Paldy, Ferencz S. Colin, Remy Heimerl, Thomas Sourjik, Victor Evolutionary Remodeling of Bacterial Motility Checkpoint Control |
title | Evolutionary Remodeling of Bacterial Motility Checkpoint Control |
title_full | Evolutionary Remodeling of Bacterial Motility Checkpoint Control |
title_fullStr | Evolutionary Remodeling of Bacterial Motility Checkpoint Control |
title_full_unstemmed | Evolutionary Remodeling of Bacterial Motility Checkpoint Control |
title_short | Evolutionary Remodeling of Bacterial Motility Checkpoint Control |
title_sort | evolutionary remodeling of bacterial motility checkpoint control |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5289928/ https://www.ncbi.nlm.nih.gov/pubmed/28122238 http://dx.doi.org/10.1016/j.celrep.2016.12.088 |
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