Literature DB >> 2464580

SecA protein autogenously represses its own translation during normal protein secretion in Escherichia coli.

M G Schmidt1, D B Oliver.   

Abstract

The Escherichia coli secA gene, whose expression is responsive to the protein secretion status of the cell, is the second gene in an operon. We found that both the basal and induced levels of SecA biosynthesis are dependent on prior translation of the upstream gene, gene X, and identified two large gene X-secA transcripts. The 10-fold derepression of secA expression by protein export defects was at the translational level since no further increases in gene X or secA mRNA levels were detected during this period, and a secA-lacZ protein fusion but not an operon fusion was appropriately derepressed. Furthermore, overexpression of the SecA protein severely reduced expression of only the secA-lacZ protein fusion, indicating that SecA autogenously represses its own translation.

Entities:  

Mesh:

Substances:

Year:  1989        PMID: 2464580      PMCID: PMC209645          DOI: 10.1128/jb.171.2.643-649.1989

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


  26 in total

1.  Feedback regulation of the spc operon in Escherichia coli: translational coupling and mRNA processing.

Authors:  L C Mattheakis; M Nomura
Journal:  J Bacteriol       Date:  1988-10       Impact factor: 3.490

2.  Lysis gene of bacteriophage MS2 is activated by translation termination at the overlapping coat gene.

Authors:  B Berkhout; B F Schmidt; A van Strien; J van Boom; J van Westrenen; J van Duin
Journal:  J Mol Biol       Date:  1987-06-05       Impact factor: 5.469

Review 3.  Transcription termination and the regulation of gene expression.

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

4.  Evidence for specificity at an early step in protein export in Escherichia coli.

Authors:  C A Kumamoto; J Beckwith
Journal:  J Bacteriol       Date:  1985-07       Impact factor: 3.490

5.  Mutational alterations of translational coupling in the L11 ribosomal protein operon of Escherichia coli.

Authors:  F Sor; M Bolotin-Fukuhara; M Nomura
Journal:  J Bacteriol       Date:  1987-08       Impact factor: 3.490

6.  secD, a new gene involved in protein export in Escherichia coli.

Authors:  C Gardel; S Benson; J Hunt; S Michaelis; J Beckwith
Journal:  J Bacteriol       Date:  1987-03       Impact factor: 3.490

7.  Effects of secA mutations on the synthesis and secretion of proteins in Escherichia coli. Evidence for a major export system for cell envelope proteins.

Authors:  L R Liss; D B Oliver
Journal:  J Biol Chem       Date:  1986-02-15       Impact factor: 5.157

8.  Signal sequence mutations disrupt feedback between secretion of an exported protein and its synthesis in E. coli.

Authors:  C A Kumamoto; D B Oliver; J Beckwith
Journal:  Nature       Date:  1984 Apr 26-May 2       Impact factor: 49.962

9.  The SecY membrane component of the bacterial protein export machinery: analysis by new electrophoretic methods for integral membrane proteins.

Authors:  Y Akiyama; K Ito
Journal:  EMBO J       Date:  1985-12-01       Impact factor: 11.598

10.  A defined mutation in the protein export gene within the spc ribosomal protein operon of Escherichia coli: isolation and characterization of a new temperature-sensitive secY mutant.

Authors:  K Shiba; K Ito; T Yura; D P Cerretti
Journal:  EMBO J       Date:  1984-03       Impact factor: 11.598

View more
  31 in total

1.  A mutant hunt for defects in membrane protein assembly yields mutations affecting the bacterial signal recognition particle and Sec machinery.

Authors:  H Tian; D Boyd; J Beckwith
Journal:  Proc Natl Acad Sci U S A       Date:  2000-04-25       Impact factor: 11.205

2.  Critical regions of secM that control its translation and secretion and promote secretion-specific secA regulation.

Authors:  Shameema Sarker; Donald Oliver
Journal:  J Bacteriol       Date:  2002-05       Impact factor: 3.490

3.  Revised translation start site for secM defines an atypical signal peptide that regulates Escherichia coli secA expression.

Authors:  S Sarker; K E Rudd; D Oliver
Journal:  J Bacteriol       Date:  2000-10       Impact factor: 3.490

4.  Overproduction of SecA suppresses the export defect caused by a mutation in the gene encoding the Escherichia coli export chaperone secB.

Authors:  H A Cook; C A Kumamoto
Journal:  J Bacteriol       Date:  1999-05       Impact factor: 3.490

5.  Translocon "pulling" of nascent SecM controls the duration of its translational pause and secretion-responsive secA regulation.

Authors:  Martha E Butkus; Lucia B Prundeanu; Donald B Oliver
Journal:  J Bacteriol       Date:  2003-11       Impact factor: 3.490

Review 6.  The sec and prl genes of Escherichia coli.

Authors:  K L Bieker; G J Phillips; T J Silhavy
Journal:  J Bioenerg Biomembr       Date:  1990-06       Impact factor: 2.945

7.  SecM facilitates translocase function of SecA by localizing its biosynthesis.

Authors:  Hitoshi Nakatogawa; Akiko Murakami; Hiroyuki Mori; Koreaki Ito
Journal:  Genes Dev       Date:  2005-02-15       Impact factor: 11.361

8.  The first gene in the Escherichia coli secA operon, gene X, encodes a nonessential secretory protein.

Authors:  T Rajapandi; K M Dolan; D B Oliver
Journal:  J Bacteriol       Date:  1991-11       Impact factor: 3.490

9.  Regulation of Escherichia coli secA mRNA translation by a secretion-responsive element.

Authors:  M G Schmidt; K M Dolan; D B Oliver
Journal:  J Bacteriol       Date:  1991-10       Impact factor: 3.490

10.  A ribosome-nascent chain sensor of membrane protein biogenesis in Bacillus subtilis.

Authors:  Shinobu Chiba; Anne Lamsa; Kit Pogliano
Journal:  EMBO J       Date:  2009-09-24       Impact factor: 11.598

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.