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Multiple sources of slow activity fluctuations in a bacterial chemosensory network
Cellular networks are intrinsically subject to stochastic fluctuations, but analysis of the resulting noise remained largely limited to gene expression. The pathway controlling chemotaxis of Escherichia coli provides one example where posttranslational signaling noise has been deduced from cellular...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5809148/ https://www.ncbi.nlm.nih.gov/pubmed/29231168 http://dx.doi.org/10.7554/eLife.26796 |
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author | Colin, Remy Rosazza, Christelle Vaknin, Ady Sourjik, Victor |
author_facet | Colin, Remy Rosazza, Christelle Vaknin, Ady Sourjik, Victor |
author_sort | Colin, Remy |
collection | PubMed |
description | Cellular networks are intrinsically subject to stochastic fluctuations, but analysis of the resulting noise remained largely limited to gene expression. The pathway controlling chemotaxis of Escherichia coli provides one example where posttranslational signaling noise has been deduced from cellular behavior. This noise was proposed to result from stochasticity in chemoreceptor methylation, and it is believed to enhance environment exploration by bacteria. Here we combined single-cell FRET measurements with analysis based on the fluctuation-dissipation theorem (FDT) to characterize origins of activity fluctuations within the chemotaxis pathway. We observed surprisingly large methylation-independent thermal fluctuations of receptor activity, which contribute to noise comparably to the energy-consuming methylation dynamics. Interactions between clustered receptors involved in amplification of chemotactic signals are also necessary to produce the observed large activity fluctuations. Our work thus shows that the high response sensitivity of this cellular pathway also increases its susceptibility to noise, from thermal and out-of-equilibrium processes. |
format | Online Article Text |
id | pubmed-5809148 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-58091482018-02-14 Multiple sources of slow activity fluctuations in a bacterial chemosensory network Colin, Remy Rosazza, Christelle Vaknin, Ady Sourjik, Victor eLife Computational and Systems Biology Cellular networks are intrinsically subject to stochastic fluctuations, but analysis of the resulting noise remained largely limited to gene expression. The pathway controlling chemotaxis of Escherichia coli provides one example where posttranslational signaling noise has been deduced from cellular behavior. This noise was proposed to result from stochasticity in chemoreceptor methylation, and it is believed to enhance environment exploration by bacteria. Here we combined single-cell FRET measurements with analysis based on the fluctuation-dissipation theorem (FDT) to characterize origins of activity fluctuations within the chemotaxis pathway. We observed surprisingly large methylation-independent thermal fluctuations of receptor activity, which contribute to noise comparably to the energy-consuming methylation dynamics. Interactions between clustered receptors involved in amplification of chemotactic signals are also necessary to produce the observed large activity fluctuations. Our work thus shows that the high response sensitivity of this cellular pathway also increases its susceptibility to noise, from thermal and out-of-equilibrium processes. eLife Sciences Publications, Ltd 2017-12-12 /pmc/articles/PMC5809148/ /pubmed/29231168 http://dx.doi.org/10.7554/eLife.26796 Text en © 2017, Colin et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Computational and Systems Biology Colin, Remy Rosazza, Christelle Vaknin, Ady Sourjik, Victor Multiple sources of slow activity fluctuations in a bacterial chemosensory network |
title | Multiple sources of slow activity fluctuations in a bacterial chemosensory network |
title_full | Multiple sources of slow activity fluctuations in a bacterial chemosensory network |
title_fullStr | Multiple sources of slow activity fluctuations in a bacterial chemosensory network |
title_full_unstemmed | Multiple sources of slow activity fluctuations in a bacterial chemosensory network |
title_short | Multiple sources of slow activity fluctuations in a bacterial chemosensory network |
title_sort | multiple sources of slow activity fluctuations in a bacterial chemosensory network |
topic | Computational and Systems Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5809148/ https://www.ncbi.nlm.nih.gov/pubmed/29231168 http://dx.doi.org/10.7554/eLife.26796 |
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