Literature DB >> 2695391

The activity of sigma 32 is reduced under conditions of excess heat shock protein production in Escherichia coli.

D B Straus1, W A Walter, C A Gross.   

Abstract

The expression of heat shock genes in Escherichia coli is controlled by the action of an alternate sigma-factor of RNA polymerase, sigma 32, which directs core RNA polymerase to recognize the promoters for heat shock genes. After a shift from 30 degrees C to 42 degrees C, both the level of sigma 32 and transcription initiation at heat shock promoters transiently increase, indicating that heat shock gene expression is regulated by changes in the concentration of sigma 32. Here, we report that heat shock gene expression is regulated by changes in the activity of sigma 32 under some conditions. Our results show that the transient repression of heat shock protein synthesis, which follows a shift down from 42 degrees C to 30 degrees, occurs as a result of decreased transcription initiation at heat shock promoters, but this repression is accompanied by only a small decrease in the level of sigma 32. In addition, the induction of heat shock proteins following overproduction of sigma 32 from a multicopy plasmid is only transient, despite the fact that the level of sigma 32 remains elevated. Constitutive overproduction of sigma 32 also fails to cause a proportionate increase in heat shock gene transcription. These three examples suggest that the activity of sigma 32 is reduced under conditions of excess heat shock gene expression.

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Year:  1989        PMID: 2695391     DOI: 10.1101/gad.3.12a.2003

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


  41 in total

1.  The Cpx envelope stress response is controlled by amplification and feedback inhibition.

Authors:  T L Raivio; D L Popkin; T J Silhavy
Journal:  J Bacteriol       Date:  1999-09       Impact factor: 3.490

2.  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

3.  Antisense downregulation of sigma(32) as a transient metabolic controller in Escherichia coli: effects on yield of active organophosphorus hydrolase.

Authors:  R Srivastava; H J Cha; M S Peterson; W E Bentley
Journal:  Appl Environ Microbiol       Date:  2000-10       Impact factor: 4.792

4.  Regulation of the alternative sigma factor sigma(E) during initiation, adaptation, and shutoff of the extracytoplasmic heat shock response in Escherichia coli.

Authors:  Sarah E Ades; Irina L Grigorova; Carol A Gross
Journal:  J Bacteriol       Date:  2003-04       Impact factor: 3.490

5.  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

6.  DnaK, DnaJ, and GrpE are required for flagellum synthesis in Escherichia coli.

Authors:  W Shi; Y Zhou; J Wild; J Adler; C A Gross
Journal:  J Bacteriol       Date:  1992-10       Impact factor: 3.490

Review 7.  Signal transduction and regulatory mechanisms involved in control of the sigma(S) (RpoS) subunit of RNA polymerase.

Authors:  Regine Hengge-Aronis
Journal:  Microbiol Mol Biol Rev       Date:  2002-09       Impact factor: 11.056

Review 8.  Regulation by proteolysis: energy-dependent proteases and their targets.

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

Review 9.  Regulated proteolysis in Gram-negative bacteria--how and when?

Authors:  Eyal Gur; Dvora Biran; Eliora Z Ron
Journal:  Nat Rev Microbiol       Date:  2011-10-24       Impact factor: 60.633

10.  Suppression of a dnaKJ deletion by multicopy dksA results from non-feedback-regulated transcripts that originate upstream of the major dksA promoter.

Authors:  Pete Chandrangsu; Li Wang; Sang Ho Choi; Richard L Gourse
Journal:  J Bacteriol       Date:  2012-01-20       Impact factor: 3.490

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