PMID:11889089

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Citation

Atlung, T and Hansen, FG (2002) Effect of different concentrations of H-NS protein on chromosome replication and the cell cycle in Escherichia coli. J. Bacteriol. 184:1843-50

Abstract

Flow cytometric analysis showed that the hns205 and hns206 mutants, lacking the abundant nucleoid-associated protein H-NS, have decreased origin concentration, as well as a low number of origins per cell (ploidy). The most striking observation was that the low ploidy was due to a very short replication time, e.g., at 30 degrees C it was halved compared to that of the hns(+) strain. The decreased origin concentration was not caused by a decreased dnaA gene expression, and the hns206 mutant had normal DnaA protein concentrations. The replication phenotypes of the hns206 mutant were independent of RpoS. Cells overproducing H-NS from a LacI-controlled plasmid had a normal origin concentration, indicating that H-NS is not controlling initiation. A wild-type H-NS concentration is, however, required to obtain a wild-type origin concentration, since cells with an intermediate H-NS concentration had an intermediate origin concentration. Two lines of evidence point to an indirect effect of H-NS on initiation. First, H-NS did not show high-affinity binding to any part of oriC, and H-NS had no effect on transcription entering oriC from the mioC promoter. Second, in a shift experiment with the hns206 mutant, when H-NS protein was induced to wild-type levels within 10 min, it took more than one generation before the origin concentration started to increase.

Links

PubMed PMC134913

Keywords

Bacterial Proteins/biosynthesis; Bacterial Proteins/genetics; Bacterial Proteins/metabolism; Binding Sites; Cell Cycle/drug effects; Chromosomes, Bacterial/drug effects; Chromosomes, Bacterial/physiology; DNA Replication/drug effects; DNA-Binding Proteins/biosynthesis; DNA-Binding Proteins/genetics; DNA-Binding Proteins/metabolism; DNA-Binding Proteins/pharmacology; Dose-Response Relationship, Drug; Electrophoretic Mobility Shift Assay; Escherichia coli/drug effects; Escherichia coli/genetics; Escherichia coli Proteins; Flavoproteins; Gene Expression/drug effects; Kinetics; Origin Recognition Complex; Phenotype; Sigma Factor/metabolism; Temperature; Transcription, Genetic/drug effects; Viral Proteins/metabolism

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