Literature DB >> 1597410

Identification of the promoter region of the Escherichia coli major cold shock gene, cspA.

H Tanabe1, J Goldstein, M Yang, M Inouye.   

Abstract

The major cold shock protein of Escherichia coli, CS7.4, is produced at a level of 13% of total protein synthesis upon a temperature shift from 37 to 10 degrees C. The transcription of its gene (cspA) was found to be tightly regulated and induced only at low temperature. In addition, the cspA mRNA was extremely unstable at 37 degrees C, so that CS7.4 production was hardly detected when the culture temperature was shifted from 15 degrees C to 37 degrees C. The transcription initiation site (+1) was identified. In vivo footprinting demonstrated that the region from bases -35 to -73 was protected from chemical modification, and gel mobility shift analysis showed that a cold-shocked cell extract contained a factor(s) specifically bound to the fragment containing the sequence between bases -63 and -92. This factor was synthesized de novo only at low temperature, and its synthesis was inhibited by chloramphenicol. Possible functions of this factor are discussed.

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Year:  1992        PMID: 1597410      PMCID: PMC206093          DOI: 10.1128/jb.174.12.3867-3873.1992

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


  23 in total

1.  Role of eukaryotic-type functional domains found in the prokaryotic enhancer receptor factor sigma 54.

Authors:  S Sasse-Dwight; J D Gralla
Journal:  Cell       Date:  1990-09-07       Impact factor: 41.582

2.  Major cold shock protein of Escherichia coli.

Authors:  J Goldstein; N S Pollitt; M Inouye
Journal:  Proc Natl Acad Sci U S A       Date:  1990-01       Impact factor: 11.205

3.  Enhancement of protein translocation across the membrane by specific mutations in the hydrophobic region of the signal peptide.

Authors:  J Goldstein; S Lehnhardt; M Inouye
Journal:  J Bacteriol       Date:  1990-03       Impact factor: 3.490

4.  Cold shock and DNA binding.

Authors:  G Wistow
Journal:  Nature       Date:  1990-04-26       Impact factor: 49.962

5.  Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction.

Authors:  P Chomczynski; N Sacchi
Journal:  Anal Biochem       Date:  1987-04       Impact factor: 3.365

6.  A simple high-resolution procedure to study DNA methylation and in vivo DNA-protein interactions on a single-copy gene level in higher eukaryotes.

Authors:  H Saluz; J P Jost
Journal:  Proc Natl Acad Sci U S A       Date:  1989-04       Impact factor: 11.205

7.  Characterization of the cDNA encoding a protein binding to the major histocompatibility complex class II Y box.

Authors:  D K Didier; J Schiffenbauer; S L Woulfe; M Zacheis; B D Schwartz
Journal:  Proc Natl Acad Sci U S A       Date:  1988-10       Impact factor: 11.205

8.  Mitotic recombination in germ cells generated two major histocompatibility complex mutant genes shown to be identical by RNA sequence analysis: Kbm9 and Kbm6.

Authors:  J Geliebter; R A Zeff; R W Melvold; S G Nathenson
Journal:  Proc Natl Acad Sci U S A       Date:  1986-05       Impact factor: 11.205

9.  Two human genes isolated by a novel method encode DNA-binding proteins containing a common region of homology.

Authors:  H Sakura; T Maekawa; F Imamoto; K Yasuda; S Ishii
Journal:  Gene       Date:  1988-12-20       Impact factor: 3.688

10.  Growth-rate dependent regulation of mRNA stability in Escherichia coli.

Authors:  G Nilsson; J G Belasco; S N Cohen; A von Gabain
Journal:  Nature       Date:  1984 Nov 1-7       Impact factor: 49.962

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  42 in total

1.  Mutation analysis of the 5' untranslated region of the cold shock cspA mRNA of Escherichia coli.

Authors:  K Yamanaka; M Mitta; M Inouye
Journal:  J Bacteriol       Date:  1999-10       Impact factor: 3.490

2.  Selective mRNA degradation by polynucleotide phosphorylase in cold shock adaptation in Escherichia coli.

Authors:  K Yamanaka; M Inouye
Journal:  J Bacteriol       Date:  2001-05       Impact factor: 3.490

3.  Restart of exponential growth of cold-shocked Yersinia enterocolitica occurs after down-regulation of cspA1/A2 mRNA.

Authors:  K Neuhaus; S Rapposch; K P Francis; S Scherer
Journal:  J Bacteriol       Date:  2000-06       Impact factor: 3.490

4.  Massive presence of the Escherichia coli 'major cold-shock protein' CspA under non-stress conditions.

Authors:  A Brandi; R Spurio; C O Gualerzi; C L Pon
Journal:  EMBO J       Date:  1999-03-15       Impact factor: 11.598

5.  Cold shock induction of the cspL gene in Lactobacillus plantarum involves transcriptional regulation.

Authors:  Sylviane Derzelle; Bernard Hallet; Thierry Ferain; Jean Delcour; Pascal Hols
Journal:  J Bacteriol       Date:  2002-10       Impact factor: 3.490

6.  Extended -10 motif is critical for activity of the cspA promoter but does not contribute to low-temperature transcription.

Authors:  Sangita Phadtare; Konstantin Severinov
Journal:  J Bacteriol       Date:  2005-09       Impact factor: 3.490

7.  Transcript analysis reveals an extended regulon and the importance of protein-protein co-operativity for the Escherichia coli methionine repressor.

Authors:  Ferenc Marincs; Iain W Manfield; Jonathan A Stead; Kenneth J McDowall; Peter G Stockley
Journal:  Biochem J       Date:  2006-06-01       Impact factor: 3.857

Review 8.  Linkage map of Escherichia coli K-12, edition 10: the traditional map.

Authors:  M K Berlyn
Journal:  Microbiol Mol Biol Rev       Date:  1998-09       Impact factor: 11.056

9.  Crystal structure of CspA, the major cold shock protein of Escherichia coli.

Authors:  H Schindelin; W Jiang; M Inouye; U Heinemann
Journal:  Proc Natl Acad Sci U S A       Date:  1994-05-24       Impact factor: 11.205

Review 10.  Strategies for achieving high-level expression of genes in Escherichia coli.

Authors:  S C Makrides
Journal:  Microbiol Rev       Date:  1996-09
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