Document Detail


Sinorhizobium meliloti CpdR1 is critical for co-ordinating cell cycle progression and the symbiotic chronic infection.
MedLine Citation:
PMID:  19602145     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
ATP-driven proteolysis plays a major role in regulating the bacterial cell cycle, development and stress responses. In the nitro -fixing symbiosis with host plants, Sinorhizobium meliloti undergoes a profound cellular differentiation, including endoreduplication of the ome. The regulatory mechanisms governing the alterations of the S. meliloti cell cycle in planta are largely unknown. Here, we report the characterization of two cpdR homologues, cpdR1 and cpdR2, of S. meliloti that encode single-domain response regulators. In Caulobacter crescentus, CpdR controls the polar localization of the ClpXP protease, thereby mediating the regulated proteolysis of key protein(s), such as CtrA, involved in cell cycle progression. The S. meliloti cpdR1-null mutant can invade the host cytoplasm, however, the intracellular bacteria are unable to differentiate into bacteroids. We show that S. meliloti CpdR1 has a polar localization pattern and a role in ClpX positioning similar to C. crescentus CpdR, suggesting a conserved function of CpdR proteins among alpha-proteobacteria. However, in S. meliloti, free-living cells of the cpdR1-null mutant show a striking morphology of irregular coccoids and aberrant DNA replication. Thus, we demonstrate that CpdR1 mediates the co-ordination of cell cycle events, which are critical for both the free-living cell division and the differentiation required for the chronic intracellular infection.
Authors:
Hajime Kobayashi; Nicole J De Nisco; Peter Chien; Lyle A Simmons; Graham C Walker
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Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't     Date:  2009-07-07
Journal Detail:
Title:  Molecular microbiology     Volume:  73     ISSN:  1365-2958     ISO Abbreviation:  Mol. Microbiol.     Publication Date:  2009 Aug 
Date Detail:
Created Date:  2009-08-19     Completed Date:  2009-10-13     Revised Date:  2010-12-03    
Medline Journal Info:
Nlm Unique ID:  8712028     Medline TA:  Mol Microbiol     Country:  England    
Other Details:
Languages:  eng     Pagination:  586-600     Citation Subset:  IM    
Affiliation:
Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
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MeSH Terms
Descriptor/Qualifier:
Bacterial Proteins / genetics,  metabolism*
Cell Cycle*
DNA Replication
DNA, Bacterial / biosynthesis
Gene Expression Profiling
Gene Expression Regulation, Bacterial
Mutagenesis, Insertional
Sinorhizobium meliloti / cytology*,  genetics,  metabolism
Symbiosis*
Grant Support
ID/Acronym/Agency:
5K99GM084157-01/GM/NIGMS NIH HHS; CA21615-27/CA/NCI NIH HHS; GM31010/GM/NIGMS NIH HHS; P30 ES002109/ES/NIEHS NIH HHS; R01 CA021615-27/CA/NCI NIH HHS
Chemical
Reg. No./Substance:
0/Bacterial Proteins; 0/DNA, Bacterial
Comments/Corrections

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