Effect of Different Concentrations of H-NS Protein on Chromosome Replication and the Cell Cycle in Escherichia coli
Open Access
- 1 April 2002
- journal article
- Published by American Society for Microbiology in Journal of Bacteriology
- Vol. 184 (7) , 1843-1850
- https://doi.org/10.1128/jb.184.7.1843-1850.2002
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°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.Keywords
This publication has 52 references indexed in Scilit:
- Use of bacteriophage T7 RNA polymerase to direct selective high-level expression of cloned genesPublished by Elsevier ,2004
- Characterisation of the allelic variation in the rpoS gene in thirteen K12 and six other non-pathogenic Escherichia coli strainsMolecular Genetics and Genomics, 2002
- A comprehensive set of DnaA‐box mutations in the replication origin, oriC, of Escherichia coliMolecular Microbiology, 1996
- The initiation mess?Molecular Microbiology, 1996
- Synthesis of the Escherichia coli K‐12 nucleoid‐associated DNA‐binding protein H‐NS is subjected to growth‐phase control and autoregulationMolecular Microbiology, 1993
- A versatile method for integration of genes and gene fusions into the λ attachment site of Escherichia coliGene, 1991
- The DnaA protein determines the initiation mass of Escherichia coli K-12Cell, 1989
- A physiological role for DNA supercoiling in the osmotic regulation of gene expression in S. typhimurium and E. coliCell, 1988
- Autoregulation of the DNA replication gene dnaA in E. coli K-12Cell, 1985
- DNA replication and the division cycle in Escherichia coliJournal of Molecular Biology, 1967