Role of the GGDEF regulator PleD in polar development of Caulobacter crescentus
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Open Access
- 5 March 2003
- journal article
- research article
- Published by Wiley in Molecular Microbiology
- Vol. 47 (6) , 1695-1708
- https://doi.org/10.1046/j.1365-2958.2003.03401.x
Abstract
Several members of the two-component signal transduction family have been implicated in the control of polar development in Caulobacter crescentus: PleC and DivJ, two polarly localized histidine sensor kinases; and the response regulators DivK and PleD. The PleD protein was shown previously to be required during the swarmer-to-stalked cell transition for flagellar ejection and efficient stalk biogenesis. Here, we present data indicating that PleD also controls the onset of motility and a cell density switch immediately preceding cell division. Constitutively active alleles of pleD or wspR, an orthologue from Pseudomonas fluorescens, almost completely suppressed C. crescentus motility and inhibited the increase in swarmer cell density during cell differentiation. The observation that these alleles also had a dominant-negative effect on motility in a pleC divJ and a pleC divK mutant background indicated that PleD is located downstream of the other components in the signal transduction cascade, which controls the activity of the flagellar motor. In addition, the presence of a constitutive pleD or wspR allele resulted in a doubling of the average stalk length. Together, this is consistent with a model in which the active form of PleD, PleD∼P, negatively controls aspects of differentiation in the late predivisional cell, whereas it acts positively on polar development during the swarmer-to-stalked cell transition. In agreement with such a model, we found that DivJ, which localizes to the stalked pole during cell differentiation, positively controlled the in vivo phosphorylation status of PleD, and the swarmer pole-specific PleC kinase modulated this status in a negative manner. Furthermore, domain switch experiments demonstrated that the WspR GGDEF output domain from P. fluorescens is active in C. crescentus, favouring a more general function for this novel signalling domain over a specific role such as DNA or protein interaction. Possible roles for PleD and its C-terminal output domain in modulating the polar cell surface of C. crescentus are discussed.Keywords
This publication has 56 references indexed in Scilit:
- MHYT, a new integral membrane sensor domainFEMS Microbiology Letters, 2001
- Genetic data indicate that proteins containing the GGDEF domain possess diguanylate cyclase activityFEMS Microbiology Letters, 2001
- Novel domains of the prokaryotic two-component signal transduction systemsFEMS Microbiology Letters, 2001
- Global Analysis of the Genetic Network Controlling a Bacterial Cell CycleScience, 2000
- Dos, a Heme-Binding PAS Protein from Escherichia coli, Is a Direct Oxygen SensorBiochemistry, 2000
- Characterization of high density monolayers of the biofilm bacterium Caulobacter crescentus: Evaluating prospects for developing immobilized cell bioreactorsCanadian Journal of Microbiology, 2000
- Signal transduction in the cell cycle regulation of Caulobacter differentiationTrends in Microbiology, 1996
- Glutamate at the Site of Phosphorylation of Nitrogen-regulatory Protein NTRC Mimics Aspartyl-Phosphate and Activates the ProteinJournal of Molecular Biology, 1993
- Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mpl8 and pUC19 vectorsGene, 1985
- A Broad Host Range Mobilization System for In Vivo Genetic Engineering: Transposon Mutagenesis in Gram Negative BacteriaBio/Technology, 1983