Literature DB >> 2771950

Negative transcriptional regulation in the Caulobacter flagellar hierarchy.

H Xu1, A Dingwall, L Shapiro.   

Abstract

The Caulobacter crescentus flagellum is formed at a specific time in the cell cycle and its assembly requires the ordered expression of a large number of genes. These genes are controlled in a positive trans-acting hierarchy that reflects the order of assembly of the flagellum. Using plasmids carrying transcriptional fusions of either a neo or a lux reporter gene to the promoters of three flagellar genes representing different ranks in the hierarchy (the hook operon, a basal body gene flbN, and the flaO gene), we have measured the level of chimeric gene expression in 13 flagellar mutant backgrounds. Mutants in the hook operon or in basal body genes caused overproduction of both hook operon and basal body gene chimeric mRNAs, suggesting that negative regulation is superimposed on the positive trans-acting control for these early events in the flagellar hierarchy. Mutants in the structural genes and in genes involved in flagellar assembly had no effect on flaO expression, placing the flaO gene near the top of the hierarchy. However, flaO expression appears to be under negative control by two regulatory genes flaS and flaW. Negative control, as a response to the completion of specific steps in the assembly process, may be an important mechanism used by the cell to turn off flagellar gene expression once the gene product is no longer needed.

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Year:  1989        PMID: 2771950      PMCID: PMC297904          DOI: 10.1073/pnas.86.17.6656

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


  36 in total

1.  Envelope-associated nucleoid from Caulobacter crescentus stalked and swarmer cells.

Authors:  M Evinger; N Agabian
Journal:  J Bacteriol       Date:  1977-10       Impact factor: 3.490

2.  Analysis of nonmotile mutants of the dimorphic bacterium Caulobacter crescentus.

Authors:  R C Johnson; B Ely
Journal:  J Bacteriol       Date:  1979-01       Impact factor: 3.490

3.  Temporal control of the cell cycle in Caulobacter crescentus: roles of DNA chain elongation and completion.

Authors:  M A Osley; A Newton
Journal:  J Mol Biol       Date:  1980-03-25       Impact factor: 5.469

4.  Cascade regulation of Caulobacter flagellar and chemotaxis genes.

Authors:  R Champer; A Dingwall; L Shapiro
Journal:  J Mol Biol       Date:  1987-03-05       Impact factor: 5.469

5.  Flagellar hook and basal complex of Caulobacter crescentus.

Authors:  R C Johnson; M P Walsh; B Ely; L Shapiro
Journal:  J Bacteriol       Date:  1979-06       Impact factor: 3.490

6.  Synthesis and structure of Caulobacter crescentus flagella.

Authors:  L Shapiro; J V Maizel
Journal:  J Bacteriol       Date:  1973-01       Impact factor: 3.490

7.  Caulobacter flagellar organelle: synthesis, compartmentation, and assembly.

Authors:  C Lagenaur; N Agabian
Journal:  J Bacteriol       Date:  1978-09       Impact factor: 3.490

8.  Membrane phospholipid composition of Caulobacter crescentus.

Authors:  I Contreras; L Shapiro; S Henry
Journal:  J Bacteriol       Date:  1978-09       Impact factor: 3.490

9.  Purification and characterization of a polyhook protein from Caulobacter crescentus.

Authors:  M Sheffery; A Newton
Journal:  J Bacteriol       Date:  1979-05       Impact factor: 3.490

10.  Generation of asymmetry during development. Segregation of type-specific proteins in Caulobacter.

Authors:  N Agabian; M Evinger; G Parker
Journal:  J Cell Biol       Date:  1979-04       Impact factor: 10.539

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  33 in total

1.  sigmaK can negatively regulate sigE expression by two different mechanisms during sporulation of Bacillus subtilis.

Authors:  B Zhang; P Struffi; L Kroos
Journal:  J Bacteriol       Date:  1999-07       Impact factor: 3.490

2.  Expression of an early gene in the flagellar regulatory hierarchy is sensitive to an interruption in DNA replication.

Authors:  A Dingwall; W Y Zhuang; K Quon; L Shapiro
Journal:  J Bacteriol       Date:  1992-03       Impact factor: 3.490

3.  Characterization of In Vivo Reporter Systems for Gene Expression and Biosensor Applications Based on luxAB Luciferase Genes.

Authors:  K Blouin; S G Walker; J Smit; R Turner
Journal:  Appl Environ Microbiol       Date:  1996-06       Impact factor: 4.792

4.  Characterization of the Caulobacter crescentus flbF promoter and identification of the inferred FlbF product as a homolog of the LcrD protein from a Yersinia enterocolitica virulence plasmid.

Authors:  L A Sanders; S Van Way; D A Mullin
Journal:  J Bacteriol       Date:  1992-02       Impact factor: 3.490

5.  Transcriptional analysis of the flagellar regulon of Salmonella typhimurium.

Authors:  K Kutsukake; Y Ohya; T Iino
Journal:  J Bacteriol       Date:  1990-02       Impact factor: 3.490

6.  A new class of Caulobacter crescentus flagellar genes.

Authors:  G Leclerc; S P Wang; B Ely
Journal:  J Bacteriol       Date:  1998-10       Impact factor: 3.490

7.  A membrane-associated protein, FliX, is required for an early step in Caulobacter flagellar assembly.

Authors:  C D Mohr; J K MacKichan; L Shapiro
Journal:  J Bacteriol       Date:  1998-04       Impact factor: 3.490

Review 8.  Regulation of cellular differentiation in Caulobacter crescentus.

Authors:  J W Gober; M V Marques
Journal:  Microbiol Rev       Date:  1995-03

9.  Timing of flagellar gene expression in the Caulobacter cell cycle is determined by a transcriptional cascade of positive regulatory genes.

Authors:  N Ohta; L S Chen; D A Mullin; A Newton
Journal:  J Bacteriol       Date:  1991-02       Impact factor: 3.490

10.  The cell cycle-regulated flagellar gene flbF of Caulobacter crescentus is homologous to a virulence locus (lcrD) of Yersinia pestis.

Authors:  G Ramakrishnan; J L Zhao; A Newton
Journal:  J Bacteriol       Date:  1991-11       Impact factor: 3.490

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