Literature DB >> 8376329

Chloramphenicol induces the transcription of the major cold shock gene of Escherichia coli, cspA.

W Jiang1, P Jones, M Inouye.   

Abstract

A downshift in temperature or exposure of cells to certain inhibitors of translation has been shown to induce the synthesis of cold shock proteins in Escherichia coli. We characterized the induction of the major cold shock protein (CS7.4, the product of the cspA gene) of E. coli in response to a shift from 37 to 15 degrees C and in response to the addition of chloramphenicol at 15 degrees C. A pulse-labeling assay and primer extension experiments indicated that the cold shock treatment resulted in a transient increase in the level of the cspA transcript and a transient induction of CS7.4, while the addition of chloramphenicol resulted in a constitutive increase in the level of cspA transcript and constitutive production of CS7.4. The addition of rifamycin immediately following the temperature downshift or along with the addition of chloramphenicol repressed the transcription of cspA as well as the induced production of CS7.4. Furthermore, changes in the cspA mRNA level were coincident with changes in CS7.4 synthesis. These results indicate that the expression of cspA induced by cold shock and chloramphenicol is at the level of transcription but not at the level of translation. Measurement of the half-life revealed that the cspA mRNA induced by chloramphenicol was more stable than that induced by cold shock.

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Year:  1993        PMID: 8376329      PMCID: PMC206661          DOI: 10.1128/jb.175.18.5824-5828.1993

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  24 in total

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Authors:  E Lund; N O Kjeldgaard
Journal:  Eur J Biochem       Date:  1972-07-24

Review 2.  Transcription termination and the regulation of gene expression.

Authors:  T Platt
Journal:  Annu Rev Biochem       Date:  1986       Impact factor: 23.643

3.  Induction of proteins in response to low temperature in Escherichia coli.

Authors:  P G Jones; R A VanBogelen; F C Neidhardt
Journal:  J Bacteriol       Date:  1987-05       Impact factor: 3.490

4.  Stringent control of RNA synthesis in the absence of guanosine 5'-diphosphate-3'-diphosphate.

Authors:  C C Pao; B T Dyess
Journal:  J Biol Chem       Date:  1981-03-10       Impact factor: 5.157

Review 5.  Inhibitors of ribosome functions.

Authors:  S Pestka
Journal:  Annu Rev Microbiol       Date:  1971       Impact factor: 15.500

6.  Role of positive charge on the amino-terminal region of the signal peptide in protein secretion across the membrane.

Authors:  S Inouye; X Soberon; T Franceschini; K Nakamura; K Itakura; M Inouye
Journal:  Proc Natl Acad Sci U S A       Date:  1982-06       Impact factor: 11.205

7.  The heat shock response of E. coli is regulated by changes in the concentration of sigma 32.

Authors:  D B Straus; W A Walter; C A Gross
Journal:  Nature       Date:  1987 Sep 24-30       Impact factor: 49.962

8.  Use of a lac promoter-operator fragment as a transcriptional control switch for expression of the constitutive lpp gene in Escherichia coli.

Authors:  K Nakamura; Y Masui; M Inouye
Journal:  J Mol Appl Genet       Date:  1982

9.  Correlation between RNA synthesis and ppGpp content in Escherichia coli during temperature shifts.

Authors:  E R Mackow; F N Chang
Journal:  Mol Gen Genet       Date:  1983

10.  Effects of the complete removal of basic amino acid residues from the signal peptide on secretion of lipoprotein in Escherichia coli.

Authors:  G P Vlasuk; S Inouye; H Ito; K Itakura; M Inouye
Journal:  J Biol Chem       Date:  1983-06-10       Impact factor: 5.157

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  20 in total

1.  CIRP2, a major cytoplasmic RNA-binding protein in Xenopus oocytes.

Authors:  K Matsumoto; K Aoki; N Dohmae; K Takio; M Tsujimoto
Journal:  Nucleic Acids Res       Date:  2000-12-01       Impact factor: 16.971

2.  Transcriptional profiling of colicin-induced cell death of Escherichia coli MG1655 identifies potential mechanisms by which bacteriocins promote bacterial diversity.

Authors:  Daniel Walker; Matthew Rolfe; Arthur Thompson; Geoffrey R Moore; Richard James; Jay C D Hinton; Colin Kleanthous
Journal:  J Bacteriol       Date:  2004-02       Impact factor: 3.490

3.  Single-stranded DNA binding of the cold-shock protein CspB from Bacillus subtilis: NMR mapping and mutational characterization.

Authors:  Markus Zeeb; Jochen Balbach
Journal:  Protein Sci       Date:  2003-01       Impact factor: 6.725

4.  Cold shock and cold acclimation proteins in the psychrotrophic bacterium Arthrobacter globiformis SI55.

Authors:  F Berger; N Morellet; F Menu; P Potier
Journal:  J Bacteriol       Date:  1996-06       Impact factor: 3.490

5.  The role of the 5'-end untranslated region of the mRNA for CspA, the major cold-shock protein of Escherichia coli, in cold-shock adaptation.

Authors:  W Jiang; L Fang; M Inouye
Journal:  J Bacteriol       Date:  1996-08       Impact factor: 3.490

6.  CspA, the major cold shock protein of Escherichia coli, negatively regulates its own gene expression.

Authors:  W Bae; P G Jones; M Inouye
Journal:  J Bacteriol       Date:  1997-11       Impact factor: 3.490

7.  Role of the cold-box region in the 5' untranslated region of the cspA mRNA in its transient expression at low temperature in Escherichia coli.

Authors:  L Fang; Y Hou; M Inouye
Journal:  J Bacteriol       Date:  1998-01       Impact factor: 3.490

8.  Recombinant protein expression at low temperatures under the transcriptional control of the major Escherichia coli cold shock promoter cspA.

Authors:  J A Vasina; F Baneyx
Journal:  Appl Environ Microbiol       Date:  1996-04       Impact factor: 4.792

9.  Large mutational target size for rapid emergence of bacterial persistence.

Authors:  Hany S Girgis; Kendra Harris; Saeed Tavazoie
Journal:  Proc Natl Acad Sci U S A       Date:  2012-07-16       Impact factor: 11.205

10.  capA, a cspA-like gene that encodes a cold acclimation protein in the psychrotrophic bacterium Arthrobacter globiformis SI55.

Authors:  F Berger; P Normand; P Potier
Journal:  J Bacteriol       Date:  1997-09       Impact factor: 3.490

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