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Evolution and Design Governing Signal Precision and Amplification in a Bacterial Chemosensory Pathway

Understanding the principles underlying the plasticity of signal transduction networks is fundamental to decipher the functioning of living cells. In Myxococcus xanthus, a particular chemosensory system (Frz) coordinates the activity of two separate motility systems (the A- and S-motility systems),...

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Autores principales: Guzzo, Mathilde, Agrebi, Rym, Espinosa, Leon, Baronian, Grégory, Molle, Virginie, Mauriello, Emilia M. F., Brochier-Armanet, Céline, Mignot, Tâm
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4546325/
https://www.ncbi.nlm.nih.gov/pubmed/26291327
http://dx.doi.org/10.1371/journal.pgen.1005460
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author Guzzo, Mathilde
Agrebi, Rym
Espinosa, Leon
Baronian, Grégory
Molle, Virginie
Mauriello, Emilia M. F.
Brochier-Armanet, Céline
Mignot, Tâm
author_facet Guzzo, Mathilde
Agrebi, Rym
Espinosa, Leon
Baronian, Grégory
Molle, Virginie
Mauriello, Emilia M. F.
Brochier-Armanet, Céline
Mignot, Tâm
author_sort Guzzo, Mathilde
collection PubMed
description Understanding the principles underlying the plasticity of signal transduction networks is fundamental to decipher the functioning of living cells. In Myxococcus xanthus, a particular chemosensory system (Frz) coordinates the activity of two separate motility systems (the A- and S-motility systems), promoting multicellular development. This unusual structure asks how signal is transduced in a branched signal transduction pathway. Using combined evolution-guided and single cell approaches, we successfully uncoupled the regulations and showed that the A-motility regulation system branched-off an existing signaling system that initially only controlled S-motility. Pathway branching emerged in part following a gene duplication event and changes in the circuit structure increasing the signaling efficiency. In the evolved pathway, the Frz histidine kinase generates a steep biphasic response to increasing external stimulations, which is essential for signal partitioning to the motility systems. We further show that this behavior results from the action of two accessory response regulator proteins that act independently to filter and amplify signals from the upstream kinase. Thus, signal amplification loops may underlie the emergence of new connectivity in signal transduction pathways.
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spelling pubmed-45463252015-08-26 Evolution and Design Governing Signal Precision and Amplification in a Bacterial Chemosensory Pathway Guzzo, Mathilde Agrebi, Rym Espinosa, Leon Baronian, Grégory Molle, Virginie Mauriello, Emilia M. F. Brochier-Armanet, Céline Mignot, Tâm PLoS Genet Research Article Understanding the principles underlying the plasticity of signal transduction networks is fundamental to decipher the functioning of living cells. In Myxococcus xanthus, a particular chemosensory system (Frz) coordinates the activity of two separate motility systems (the A- and S-motility systems), promoting multicellular development. This unusual structure asks how signal is transduced in a branched signal transduction pathway. Using combined evolution-guided and single cell approaches, we successfully uncoupled the regulations and showed that the A-motility regulation system branched-off an existing signaling system that initially only controlled S-motility. Pathway branching emerged in part following a gene duplication event and changes in the circuit structure increasing the signaling efficiency. In the evolved pathway, the Frz histidine kinase generates a steep biphasic response to increasing external stimulations, which is essential for signal partitioning to the motility systems. We further show that this behavior results from the action of two accessory response regulator proteins that act independently to filter and amplify signals from the upstream kinase. Thus, signal amplification loops may underlie the emergence of new connectivity in signal transduction pathways. Public Library of Science 2015-08-20 /pmc/articles/PMC4546325/ /pubmed/26291327 http://dx.doi.org/10.1371/journal.pgen.1005460 Text en © 2015 Guzzo et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Guzzo, Mathilde
Agrebi, Rym
Espinosa, Leon
Baronian, Grégory
Molle, Virginie
Mauriello, Emilia M. F.
Brochier-Armanet, Céline
Mignot, Tâm
Evolution and Design Governing Signal Precision and Amplification in a Bacterial Chemosensory Pathway
title Evolution and Design Governing Signal Precision and Amplification in a Bacterial Chemosensory Pathway
title_full Evolution and Design Governing Signal Precision and Amplification in a Bacterial Chemosensory Pathway
title_fullStr Evolution and Design Governing Signal Precision and Amplification in a Bacterial Chemosensory Pathway
title_full_unstemmed Evolution and Design Governing Signal Precision and Amplification in a Bacterial Chemosensory Pathway
title_short Evolution and Design Governing Signal Precision and Amplification in a Bacterial Chemosensory Pathway
title_sort evolution and design governing signal precision and amplification in a bacterial chemosensory pathway
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4546325/
https://www.ncbi.nlm.nih.gov/pubmed/26291327
http://dx.doi.org/10.1371/journal.pgen.1005460
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