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Coordination of Division and Development Influences Complex Multicellular Behavior in Agrobacterium tumefaciens

The α-Proteobacterium Agrobacterium tumefaciens has proteins homologous to known regulators that govern cell division and development in Caulobacter crescentus, many of which are also conserved among diverse α-Proteobacteria. In light of recent work demonstrating similarity between the division cycl...

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Autores principales: Kim, Jinwoo, Heindl, Jason E., Fuqua, Clay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3577659/
https://www.ncbi.nlm.nih.gov/pubmed/23437210
http://dx.doi.org/10.1371/journal.pone.0056682
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author Kim, Jinwoo
Heindl, Jason E.
Fuqua, Clay
author_facet Kim, Jinwoo
Heindl, Jason E.
Fuqua, Clay
author_sort Kim, Jinwoo
collection PubMed
description The α-Proteobacterium Agrobacterium tumefaciens has proteins homologous to known regulators that govern cell division and development in Caulobacter crescentus, many of which are also conserved among diverse α-Proteobacteria. In light of recent work demonstrating similarity between the division cycle of C. crescentus and that of A. tumefaciens, the functional conservation for this presumptive control pathway was examined. In C. crescentus the CtrA response regulator serves as the master regulator of cell cycle progression and cell division. CtrA activity is controlled by an integrated pair of multi-component phosphorelays: PleC/DivJ-DivK and CckA-ChpT-CtrA. Although several of the conserved orthologues appear to be essential in A. tumefaciens, deletions in pleC or divK were isolated and resulted in cell division defects, diminished swimming motility, and a decrease in biofilm formation. A. tumefaciens also has two additional pleC/divJ homologue sensor kinases called pdhS1 and pdhS2, absent in C. crescentus. Deletion of pdhS1 phenocopied the ΔpleC and ΔdivK mutants. Cells lacking pdhS2 morphologically resembled wild-type bacteria, but were decreased in swimming motility and elevated for biofilm formation, suggesting that pdhS2 may serve to regulate the motile to non-motile switch in A. tumefaciens. Genetic analysis suggests that the PleC/DivJ-DivK and CckA-ChpT-CtrA phosphorelays in A. tumefaciens are vertically-integrated, as in C. crescentus. A gain-of-function mutation in CckA (Y674D) was identified as a spontaneous suppressor of the ΔpleC motility phenotype. Thus, although the core architecture of the A. tumefaciens pathway resembles that of C. crescentus there are specific differences including additional regulators, divergent pathway architecture, and distinct target functions.
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spelling pubmed-35776592013-02-22 Coordination of Division and Development Influences Complex Multicellular Behavior in Agrobacterium tumefaciens Kim, Jinwoo Heindl, Jason E. Fuqua, Clay PLoS One Research Article The α-Proteobacterium Agrobacterium tumefaciens has proteins homologous to known regulators that govern cell division and development in Caulobacter crescentus, many of which are also conserved among diverse α-Proteobacteria. In light of recent work demonstrating similarity between the division cycle of C. crescentus and that of A. tumefaciens, the functional conservation for this presumptive control pathway was examined. In C. crescentus the CtrA response regulator serves as the master regulator of cell cycle progression and cell division. CtrA activity is controlled by an integrated pair of multi-component phosphorelays: PleC/DivJ-DivK and CckA-ChpT-CtrA. Although several of the conserved orthologues appear to be essential in A. tumefaciens, deletions in pleC or divK were isolated and resulted in cell division defects, diminished swimming motility, and a decrease in biofilm formation. A. tumefaciens also has two additional pleC/divJ homologue sensor kinases called pdhS1 and pdhS2, absent in C. crescentus. Deletion of pdhS1 phenocopied the ΔpleC and ΔdivK mutants. Cells lacking pdhS2 morphologically resembled wild-type bacteria, but were decreased in swimming motility and elevated for biofilm formation, suggesting that pdhS2 may serve to regulate the motile to non-motile switch in A. tumefaciens. Genetic analysis suggests that the PleC/DivJ-DivK and CckA-ChpT-CtrA phosphorelays in A. tumefaciens are vertically-integrated, as in C. crescentus. A gain-of-function mutation in CckA (Y674D) was identified as a spontaneous suppressor of the ΔpleC motility phenotype. Thus, although the core architecture of the A. tumefaciens pathway resembles that of C. crescentus there are specific differences including additional regulators, divergent pathway architecture, and distinct target functions. Public Library of Science 2013-02-20 /pmc/articles/PMC3577659/ /pubmed/23437210 http://dx.doi.org/10.1371/journal.pone.0056682 Text en © 2013 Kim 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
Kim, Jinwoo
Heindl, Jason E.
Fuqua, Clay
Coordination of Division and Development Influences Complex Multicellular Behavior in Agrobacterium tumefaciens
title Coordination of Division and Development Influences Complex Multicellular Behavior in Agrobacterium tumefaciens
title_full Coordination of Division and Development Influences Complex Multicellular Behavior in Agrobacterium tumefaciens
title_fullStr Coordination of Division and Development Influences Complex Multicellular Behavior in Agrobacterium tumefaciens
title_full_unstemmed Coordination of Division and Development Influences Complex Multicellular Behavior in Agrobacterium tumefaciens
title_short Coordination of Division and Development Influences Complex Multicellular Behavior in Agrobacterium tumefaciens
title_sort coordination of division and development influences complex multicellular behavior in agrobacterium tumefaciens
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3577659/
https://www.ncbi.nlm.nih.gov/pubmed/23437210
http://dx.doi.org/10.1371/journal.pone.0056682
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