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Integrative and quantitative view of the CtrA regulatory network in a stalked budding bacterium

The Alphaproteobacteria show a remarkable diversity of cell cycle-dependent developmental patterns, which are governed by the conserved CtrA pathway. Its central component CtrA is a DNA-binding response regulator that is controlled by a complex two-component signaling network, mediating distinct tra...

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Autores principales: Leicht, Oliver, van Teeseling, Muriel C. F., Panis, Gaël, Reif, Celine, Wendt, Heiko, Viollier, Patrick H., Thanbichler, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7200025/
https://www.ncbi.nlm.nih.gov/pubmed/32324740
http://dx.doi.org/10.1371/journal.pgen.1008724
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author Leicht, Oliver
van Teeseling, Muriel C. F.
Panis, Gaël
Reif, Celine
Wendt, Heiko
Viollier, Patrick H.
Thanbichler, Martin
author_facet Leicht, Oliver
van Teeseling, Muriel C. F.
Panis, Gaël
Reif, Celine
Wendt, Heiko
Viollier, Patrick H.
Thanbichler, Martin
author_sort Leicht, Oliver
collection PubMed
description The Alphaproteobacteria show a remarkable diversity of cell cycle-dependent developmental patterns, which are governed by the conserved CtrA pathway. Its central component CtrA is a DNA-binding response regulator that is controlled by a complex two-component signaling network, mediating distinct transcriptional programs in the two offspring. The CtrA pathway has been studied intensively and was shown to consist of an upstream part that reads out the developmental state of the cell and a downstream part that integrates the upstream signals and mediates CtrA phosphorylation. However, the role of this circuitry in bacterial diversification remains incompletely understood. We have therefore investigated CtrA regulation in the morphologically complex stalked budding alphaproteobacterium Hyphomonas neptunium. Compared to relatives dividing by binary fission, H. neptunium shows distinct changes in the role and regulation of various pathway components. Most notably, the response regulator DivK, which normally links the upstream and downstream parts of the CtrA pathway, is dispensable, while downstream components such as the pseudokinase DivL, the histidine kinase CckA, the phosphotransferase ChpT and CtrA are essential. Moreover, CckA is compartmentalized to the nascent bud without forming distinct polar complexes and CtrA is not regulated at the level of protein abundance. We show that the downstream pathway controls critical functions such as replication initiation, cell division and motility. Quantification of the signal flow through different nodes of the regulatory cascade revealed that the CtrA pathway is a leaky pipeline and must involve thus-far unidentified factors. Collectively, the quantitative system-level analysis of CtrA regulation in H. neptunium points to a considerable evolutionary plasticity of cell cycle regulation in alphaproteobacteria and leads to hypotheses that may also hold in well-established model organisms such as Caulobacter crescentus.
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spelling pubmed-72000252020-05-12 Integrative and quantitative view of the CtrA regulatory network in a stalked budding bacterium Leicht, Oliver van Teeseling, Muriel C. F. Panis, Gaël Reif, Celine Wendt, Heiko Viollier, Patrick H. Thanbichler, Martin PLoS Genet Research Article The Alphaproteobacteria show a remarkable diversity of cell cycle-dependent developmental patterns, which are governed by the conserved CtrA pathway. Its central component CtrA is a DNA-binding response regulator that is controlled by a complex two-component signaling network, mediating distinct transcriptional programs in the two offspring. The CtrA pathway has been studied intensively and was shown to consist of an upstream part that reads out the developmental state of the cell and a downstream part that integrates the upstream signals and mediates CtrA phosphorylation. However, the role of this circuitry in bacterial diversification remains incompletely understood. We have therefore investigated CtrA regulation in the morphologically complex stalked budding alphaproteobacterium Hyphomonas neptunium. Compared to relatives dividing by binary fission, H. neptunium shows distinct changes in the role and regulation of various pathway components. Most notably, the response regulator DivK, which normally links the upstream and downstream parts of the CtrA pathway, is dispensable, while downstream components such as the pseudokinase DivL, the histidine kinase CckA, the phosphotransferase ChpT and CtrA are essential. Moreover, CckA is compartmentalized to the nascent bud without forming distinct polar complexes and CtrA is not regulated at the level of protein abundance. We show that the downstream pathway controls critical functions such as replication initiation, cell division and motility. Quantification of the signal flow through different nodes of the regulatory cascade revealed that the CtrA pathway is a leaky pipeline and must involve thus-far unidentified factors. Collectively, the quantitative system-level analysis of CtrA regulation in H. neptunium points to a considerable evolutionary plasticity of cell cycle regulation in alphaproteobacteria and leads to hypotheses that may also hold in well-established model organisms such as Caulobacter crescentus. Public Library of Science 2020-04-23 /pmc/articles/PMC7200025/ /pubmed/32324740 http://dx.doi.org/10.1371/journal.pgen.1008724 Text en © 2020 Leicht 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Leicht, Oliver
van Teeseling, Muriel C. F.
Panis, Gaël
Reif, Celine
Wendt, Heiko
Viollier, Patrick H.
Thanbichler, Martin
Integrative and quantitative view of the CtrA regulatory network in a stalked budding bacterium
title Integrative and quantitative view of the CtrA regulatory network in a stalked budding bacterium
title_full Integrative and quantitative view of the CtrA regulatory network in a stalked budding bacterium
title_fullStr Integrative and quantitative view of the CtrA regulatory network in a stalked budding bacterium
title_full_unstemmed Integrative and quantitative view of the CtrA regulatory network in a stalked budding bacterium
title_short Integrative and quantitative view of the CtrA regulatory network in a stalked budding bacterium
title_sort integrative and quantitative view of the ctra regulatory network in a stalked budding bacterium
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7200025/
https://www.ncbi.nlm.nih.gov/pubmed/32324740
http://dx.doi.org/10.1371/journal.pgen.1008724
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