Literature DB >> 3315851

Regulation of the promoters and transcripts of rpoH, the Escherichia coli heat shock regulatory gene.

J W Erickson1, V Vaughn, W A Walter, F C Neidhardt, C A Gross.   

Abstract

In Escherichia coli the product of the rpoH (htpR) gene, sigma 32, directs RNA polymerase to initiate transcription from heat shock promoters at all temperatures. Transcription of the heat shock genes is increased when cells are exposed to high temperatures because of increased transcription initiation by sigma 32-RNA polymerase. As a step toward understanding the regulation of the heat shock response we have examined the transcription of the rpoH gene. Using S1 mapping, promoter cloning, and in vitro transcription, we have identified the promoters and the terminator for the rpoH transcription unit. The rpoH transcripts are monocistronic and originate from at least three promoters. None of the promoters is recognized by sigma 32-RNA polymerase. Two are recognized by sigma 70-RNA polymerase and are active at both low and high growth temperatures. We do not know what form of RNA polymerase recognizes the third promoter. Transcripts from this promoter are abundant only at high temperature and are present after shift to the lethal temperature of 50 degrees C, even at times when there are no detectable transcripts from the other rpoH promoters. The amount of rpoH mRNA increases fivefold by 8 min after shift from 30 to 43.5 degrees C but rpoH mRNA synthesis increases by less than twofold, indicating that there is post-transcriptional control of the level of rpoH mRNA and presumably of sigma 32.

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Year:  1987        PMID: 3315851     DOI: 10.1101/gad.1.5.419

Source DB:  PubMed          Journal:  Genes Dev        ISSN: 0890-9369            Impact factor:   11.361


  79 in total

1.  The Escherichia coli sigma(E)-dependent extracytoplasmic stress response is controlled by the regulated proteolysis of an anti-sigma factor.

Authors:  S E Ades; L E Connolly; B M Alba; C A Gross
Journal:  Genes Dev       Date:  1999-09-15       Impact factor: 11.361

2.  The response to extracytoplasmic stress in Escherichia coli is controlled by partially overlapping pathways.

Authors:  L Connolly; A De Las Penas; B M Alba; C A Gross
Journal:  Genes Dev       Date:  1997-08-01       Impact factor: 11.361

3.  A large decrease in heat-shock-induced proteolysis after tryptophan starvation leads to increased expression of phage lambda lysozyme cloned in Escherichia coli.

Authors:  P Soumillion; J Fastrez
Journal:  Biochem J       Date:  1992-08-15       Impact factor: 3.857

4.  How a mutation in the gene encoding sigma 70 suppresses the defective heat shock response caused by a mutation in the gene encoding sigma 32.

Authors:  Y N Zhou; C A Gross
Journal:  J Bacteriol       Date:  1992-11       Impact factor: 3.490

Review 5.  Regulation by proteolysis: energy-dependent proteases and their targets.

Authors:  S Gottesman; M R Maurizi
Journal:  Microbiol Rev       Date:  1992-12

6.  Some effects of growth conditions on steady state and heat shock induced htpG gene expression in continuous cultures of Escherichia coli.

Authors:  A Heitzer; C A Mason; M Snozzi; G Hamer
Journal:  Arch Microbiol       Date:  1990       Impact factor: 2.552

7.  Translational regulation of sigma 32 synthesis: requirement for an internal control element.

Authors:  A S Kamath-Loeb; C A Gross
Journal:  J Bacteriol       Date:  1991-06       Impact factor: 3.490

8.  Modulation of stability of the Escherichia coli heat shock regulatory factor sigma.

Authors:  K Tilly; J Spence; C Georgopoulos
Journal:  J Bacteriol       Date:  1989-03       Impact factor: 3.490

9.  The RpoH-mediated stress response in Neisseria gonorrhoeae is regulated at the level of activity.

Authors:  Lina Laskos; Catherine S Ryan; Janet A M Fyfe; John K Davies
Journal:  J Bacteriol       Date:  2004-12       Impact factor: 3.490

10.  Analysis of promoters controlled by the putative sigma factor AlgU regulating conversion to mucoidy in Pseudomonas aeruginosa: relationship to sigma E and stress response.

Authors:  D W Martin; M J Schurr; H Yu; V Deretic
Journal:  J Bacteriol       Date:  1994-11       Impact factor: 3.490

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