» Articles » PMID: 7768855

Role for the Histone-like Protein H-NS in Growth Phase-dependent and Osmotic Regulation of Sigma S and Many Sigma S-dependent Genes in Escherichia Coli

Overview
Journal J Bacteriol
Specialty Microbiology
Date 1995 Jun 1
PMID 7768855
Citations 80
Authors
Affiliations
Soon will be listed here.
Abstract

The sigma S subunit of RNA polymerase (encoded by the rpoS gene) is the master regulator in a complex regulatory network that controls stationary-phase induction and osmotic regulation of many genes in Escherichia coli. Here we demonstrate that the histone-like protein H-NS is also a component of this network, in which it functions as a global inhibitor of gene expression during the exponential phase of growth. On two-dimensional gels, at least 22 sigma S-controlled proteins show increased expression in an hns mutant. H-NS also inhibits the expression of sigma S itself by a mechanism that acts at the posttranscriptional level. Our results indicate that relief of repression by H-NS plays a role in stationary-phase induction as well as in hyperosmotic induction of rpoS translation. Whereas certain sigma S-dependent genes (e.g., osmY) are only indirectly regulated by H-NS via its role in the control of sigma S expression, others are also H-NS-regulated in a sigma S-independent manner. (For this latter class of genes, rpoS hns double mutants show higher levels of expression than mutants deficient in rpoS alone.) In addition, we demonstrate that the slow-growth phenotype of hns mutants is suppressed in hns rpoS double mutants and that many second-site suppressor mutants that spontaneously arise from hns strains carry lesions that affect the expression of sigma S.

Citing Articles

Characterization of Bacterial Transcriptional Regulatory Networks in through Genome-Wide In Vitro Run-Off Transcription/RNA-seq (ROSE).

Schmidt P, Brandt D, Busche T, Kalinowski J Microorganisms. 2023; 11(6).

PMID: 37374890 PMC: 10301672. DOI: 10.3390/microorganisms11061388.


Degradation of gene silencer is essential for expression of foreign genes and bacterial colonization of the mammalian gut.

Choi J, Schmukler M, Groisman E Proc Natl Acad Sci U S A. 2022; 119(40):e2210239119.

PMID: 36161931 PMC: 9546599. DOI: 10.1073/pnas.2210239119.


Growth Phase-Dependent Chromosome Condensation and Heat-Stable Nucleoid-Structuring Protein Redistribution in Escherichia coli under Osmotic Stress.

Rafiei N, Cordova M, Navarre W, Milstein J J Bacteriol. 2019; 201(23).

PMID: 31481544 PMC: 6832063. DOI: 10.1128/JB.00469-19.


Genetics, Toxicity, and Distribution of Enterohemorrhagic Hemolysin.

Schwidder M, Heinisch L, Schmidt H Toxins (Basel). 2019; 11(9).

PMID: 31470552 PMC: 6784236. DOI: 10.3390/toxins11090502.


Trouble is coming: Signaling pathways that regulate general stress responses in bacteria.

Gottesman S J Biol Chem. 2019; 294(31):11685-11700.

PMID: 31197038 PMC: 6682744. DOI: 10.1074/jbc.REV119.005593.


References
1.
Tupper A, Ussery D, Santos D, Ferguson D, Sidebotham J, Hinton J . The chromatin-associated protein H-NS alters DNA topology in vitro. EMBO J. 1994; 13(1):258-68. PMC: 394800. DOI: 10.1002/j.1460-2075.1994.tb06256.x. View

2.
Yim H, Brems R, VILLAREJO M . Molecular characterization of the promoter of osmY, an rpoS-dependent gene. J Bacteriol. 1994; 176(1):100-7. PMC: 205019. DOI: 10.1128/jb.176.1.100-107.1994. View

3.
Mellies J, Brems R, VILLAREJO M . The Escherichia coli proU promoter element and its contribution to osmotically signaled transcription activation. J Bacteriol. 1994; 176(12):3638-45. PMC: 205553. DOI: 10.1128/jb.176.12.3638-3645.1994. View

4.
Takayanagi Y, Tanaka K, Takahashi H . Structure of the 5' upstream region and the regulation of the rpoS gene of Escherichia coli. Mol Gen Genet. 1994; 243(5):525-31. DOI: 10.1007/BF00284200. View

5.
Lomovskaya O, Kidwell J, Matin A . Characterization of the sigma 38-dependent expression of a core Escherichia coli starvation gene, pexB. J Bacteriol. 1994; 176(13):3928-35. PMC: 205590. DOI: 10.1128/jb.176.13.3928-3935.1994. View