Literature DB >> 6387714

Heat shock regulatory gene (htpR) of Escherichia coli is required for growth at high temperature but is dispensable at low temperature.

T Yura, T Tobe, K Ito, T Osawa.   

Abstract

Nonsense mutations affecting the positive regulatory gene (htpR) of heat shock response have been obtained in a strain of Escherichia coli carrying no suppressor. The mutants can grow only at temperatures below 34 degrees C-35 degrees C. Heat, ethanol, and coumermycin induce major heat shock proteins in the wild-type but not in the htpR mutants. In contrast, the level of heat shock proteins synthesized at low temperature is unaffected. The htpR gene product is thus required for induction of heat shock proteins by heat or other stresses but not for their "basal-level" synthesis. Nucleotide sequence has been determined for the wild-type and the mutant alleles of htpR. The coding region appears to consist of 852 nucleotide pairs that correspond to 284 amino acids. Sequences commonly considered as signals for transcriptional initiation and termination were found flanking the coding region. Within this region, six amber, one opal, and two missense mutations were identified; the nonsense mutations are scattered along the gene, some being very close to the presumed amino terminus. These results indicate that the absence of htpR gene product is directly responsible for the failure to respond to heat shock or other stresses and for the inability to grow at high temperature. We propose that htpR represents a new class of genes that are essential for growth only at high temperatures (greater than 35 degrees C). Implications of the sequence homologies found among htpR, rpoD, and nusA proteins are discussed.

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Year:  1984        PMID: 6387714      PMCID: PMC392020          DOI: 10.1073/pnas.81.21.6803

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  20 in total

1.  Evidence for a positive regulation of RNA polymerase synthesis in Escherichia coli.

Authors:  Y Nakamura; T Yura
Journal:  J Mol Biol       Date:  1975-10-05       Impact factor: 5.469

2.  Still more mutant tyrosine transfer ribonucleic acids.

Authors:  K W Anderson; J D Smith
Journal:  J Mol Biol       Date:  1972-08-28       Impact factor: 5.469

3.  A temperature sensitive nonsense mutation affecting the synthesis of a major protein of Escherichia coli K12.

Authors:  S Cooper; T Ruettinger
Journal:  Mol Gen Genet       Date:  1975-08-05

4.  Interaction of the sigma factor and the nusA gene protein of E. coli with RNA polymerase in the initiation-termination cycle of transcription.

Authors:  J Greenblatt; J Li
Journal:  Cell       Date:  1981-05       Impact factor: 41.582

5.  Positive regulatory gene for temperature-controlled proteins in Escherichia coli.

Authors:  F C Neidhardt; R A VanBogelen
Journal:  Biochem Biophys Res Commun       Date:  1981-05-29       Impact factor: 3.575

6.  A system for shotgun DNA sequencing.

Authors:  J Messing; R Crea; P H Seeburg
Journal:  Nucleic Acids Res       Date:  1981-01-24       Impact factor: 16.971

7.  Temperature-induced synthesis of specific proteins in Escherichia coli: evidence for transcriptional control.

Authors:  T Yamamori; T Yura
Journal:  J Bacteriol       Date:  1980-06       Impact factor: 3.490

8.  DNA sequencing with chain-terminating inhibitors.

Authors:  F Sanger; S Nicklen; A R Coulson
Journal:  Proc Natl Acad Sci U S A       Date:  1977-12       Impact factor: 11.205

9.  Effects of reduced amount of RNA polymerase sigma factor on gene expression and growth of Escherichia coli: studies of the rpoD450 (amber) mutation.

Authors:  T Osawa; T Yura
Journal:  Mol Gen Genet       Date:  1981

10.  The nucleotide sequence of the cloned rpoD gene for the RNA polymerase sigma subunit from E coli K12.

Authors:  Z Burton; R R Burgess; J Lin; D Moore; S Holder; C A Gross
Journal:  Nucleic Acids Res       Date:  1981-06-25       Impact factor: 16.971

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  69 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.  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

3.  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

4.  Adaptation of Escherichia coli to elevated temperatures: the metA gene product is a heat shock protein.

Authors:  E Z Ron; S Alajem; D Biran; N Grossman
Journal:  Antonie Van Leeuwenhoek       Date:  1990-10       Impact factor: 2.271

Review 5.  Roles and regulation of the heat shock sigma factor sigma 32 in Escherichia coli.

Authors:  T Yura; Y Kawasaki; N Kusukawa; H Nagai; C Wada; R Yano
Journal:  Antonie Van Leeuwenhoek       Date:  1990-10       Impact factor: 2.271

6.  Phage shock protein, a stress protein of Escherichia coli.

Authors:  J L Brissette; M Russel; L Weiner; P Model
Journal:  Proc Natl Acad Sci U S A       Date:  1990-02       Impact factor: 11.205

7.  Suppression of the Escherichia coli rpoH opal mutation by ribosomes lacking S15 protein.

Authors:  R Yano; T Yura
Journal:  J Bacteriol       Date:  1989-03       Impact factor: 3.490

8.  Enhanced heterologous gene expression in novel rpoH mutants of Escherichia coli.

Authors:  M G Obukowicz; N R Staten; G G Krivi
Journal:  Appl Environ Microbiol       Date:  1992-05       Impact factor: 4.792

9.  The rpoE gene of Escherichia coli, which encodes sigma E, is essential for bacterial growth at high temperature.

Authors:  K Hiratsu; M Amemura; H Nashimoto; H Shinagawa; K Makino
Journal:  J Bacteriol       Date:  1995-05       Impact factor: 3.490

10.  Sigma 32-dependent promoter activity in vivo: sequence determinants of the groE promoter.

Authors:  Yang Wang; Pieter L deHaseth
Journal:  J Bacteriol       Date:  2003-10       Impact factor: 3.490

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