Literature DB >> 8002583

Multiple structural proteins are required for both transcriptional activation and negative autoregulation of Caulobacter crescentus flagellar genes.

G Ramakrishnan1, J L Zhao, A Newton.   

Abstract

The periodic and sequential expression of flagellar (fla) genes in the Caulobacter crescentus cell cycle depends on their organization into levels I to IV of a regulatory hierarchy in which genes at the top of the hierarchy are expressed early in the cell cycle and are required for the later expression of genes below them. In these studies, we have examined the regulatory role of level II fliF operon, which is located near the top of the hierarchy. The last gene in the fliF operon, flbD, encodes a transcriptional factor required for activation of sigma 54-dependent promoters at levels III and IV and negative autoregulation of the level II fliF promoter. We have physically mapped the fliF operon, identified four new genes in the transcription unit, and determined that the organization of these genes is 5'-fliF-fliG-flbE-fliN-flbD-3'. Three of the genes encode homologs of the MS ring protein (FliF) and two switch proteins (FliG and FliN) of enteric bacteria, and the fourth encodes a predicted protein (FlbE) without obvious similarities to known bacterial proteins. We have introduced nonpolar mutations in each of the open reading frames and shown that all of the newly identified genes (fliF, fliG, flbE, and fliN) are required in addition to flbD for activation of the sigma 54-dependent flgK and flbG promoters at level III. In contrast, fliF, fliG, and flbE, but not fliN, are required in addition to flbD for negative autoregulation of the level II fliF promoter. The simplest interpretation of these results is that the requirements of FlbD in transcriptional activation and repression are not identical, and we speculate that FlbD function is subject to dual or overlapping controls. We also discuss the requirement of multiple structural genes for regulation of levels II and III genes and suggest that fla gene expression in C. crescentus may be coupled to two checkpoints in flagellum assembly.

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Year:  1994        PMID: 8002583      PMCID: PMC197216          DOI: 10.1128/jb.176.24.7587-7600.1994

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


  69 in total

Review 1.  Genetics and biogenesis of bacterial flagella.

Authors:  R M Macnab
Journal:  Annu Rev Genet       Date:  1992       Impact factor: 16.830

2.  Flagellar switch of Salmonella typhimurium: gene sequences and deduced protein sequences.

Authors:  M Kihara; M Homma; K Kutsukake; R M Macnab
Journal:  J Bacteriol       Date:  1989-06       Impact factor: 3.490

3.  Localization of the Salmonella typhimurium flagellar switch protein FliG to the cytoplasmic M-ring face of the basal body.

Authors:  N R Francis; V M Irikura; S Yamaguchi; D J DeRosier; R M Macnab
Journal:  Proc Natl Acad Sci U S A       Date:  1992-07-15       Impact factor: 11.205

4.  Flagellar assembly in Salmonella typhimurium: analysis with temperature-sensitive mutants.

Authors:  C J Jones; R M Macnab
Journal:  J Bacteriol       Date:  1990-03       Impact factor: 3.490

5.  Identification of a gene cluster involved in flagellar basal body biogenesis in Caulobacter crescentus.

Authors:  K M Hahnenberger; L Shapiro
Journal:  J Mol Biol       Date:  1987-03-05       Impact factor: 5.469

6.  Ntr-like promoters and upstream regulatory sequence ftr are required for transcription of a developmentally regulated Caulobacter crescentus flagellar gene.

Authors:  D A Mullin; A Newton
Journal:  J Bacteriol       Date:  1989-06       Impact factor: 3.490

7.  Regulation of periodic protein synthesis in the cell cycle: control of initiation and termination of flagellar gene expression.

Authors:  M Sheffery; A Newton
Journal:  Cell       Date:  1981-04       Impact factor: 41.582

8.  Use of pulsed field gel electrophoresis and transposon mutagenesis to estimate the minimal number of genes required for motility in Caulobacter crescentus.

Authors:  B Ely; T W Ely
Journal:  Genetics       Date:  1989-12       Impact factor: 4.562

9.  Early Caulobacter crescentus genes fliL and fliM are required for flagellar gene expression and normal cell division.

Authors:  J Yu; L Shapiro
Journal:  J Bacteriol       Date:  1992-05       Impact factor: 3.490

10.  The nucleotide sequence of the Mr = 28,500 flagellin gene of Caulobacter crescentus.

Authors:  P R Gill; N Agabian
Journal:  J Biol Chem       Date:  1983-06-25       Impact factor: 5.157

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  21 in total

1.  Regulated expression of a highly conserved regulatory gene cluster is necessary for controlling photosynthesis gene expression in response to anaerobiosis in Rhodobacter capsulatus.

Authors:  S Du; J L Kouadio; C E Bauer
Journal:  J Bacteriol       Date:  1999-07       Impact factor: 3.490

2.  Role of the cytoplasmic C terminus of the FliF motor protein in flagellar assembly and rotation.

Authors:  Björn Grünenfelder; Stefanie Gehrig; Urs Jenal
Journal:  J Bacteriol       Date:  2003-03       Impact factor: 3.490

3.  An extreme clockwise switch bias mutation in fliG of Salmonella typhimurium and its suppression by slow-motile mutations in motA and motB.

Authors:  F Togashi; S Yamaguchi; M Kihara; S I Aizawa; R M Macnab
Journal:  J Bacteriol       Date:  1997-05       Impact factor: 3.490

4.  Intergenic suppression between the flagellar MS ring protein FliF of Salmonella and FlhA, a membrane component of its export apparatus.

Authors:  M Kihara; T Minamino; S Yamaguchi; R M Macnab
Journal:  J Bacteriol       Date:  2001-03       Impact factor: 3.490

5.  The hrpA and hrpC operons of Erwinia amylovora encode components of a type III pathway that secretes harpin.

Authors:  J F Kim; Z M Wei; S V Beer
Journal:  J Bacteriol       Date:  1997-03       Impact factor: 3.490

6.  Erwinia amylovora secretes harpin via a type III pathway and contains a homolog of yopN of Yersinia spp.

Authors:  A J Bogdanove; Z M Wei; L Zhao; S V Beer
Journal:  J Bacteriol       Date:  1996-03       Impact factor: 3.490

7.  Isolation and characterization of a xylose-dependent promoter from Caulobacter crescentus.

Authors:  A C Meisenzahl; L Shapiro; U Jenal
Journal:  J Bacteriol       Date:  1997-02       Impact factor: 3.490

8.  fleN, a gene that regulates flagellar number in Pseudomonas aeruginosa.

Authors:  N Dasgupta; S K Arora; R Ramphal
Journal:  J Bacteriol       Date:  2000-01       Impact factor: 3.490

9.  Cloning and phenotypic characterization of fleS and fleR, new response regulators of Pseudomonas aeruginosa which regulate motility and adhesion to mucin.

Authors:  B W Ritchings; E C Almira; S Lory; R Ramphal
Journal:  Infect Immun       Date:  1995-12       Impact factor: 3.441

10.  Cloning, sequencing, and phenotypic analysis of laf1, encoding the flagellin of the lateral flagella of Azospirillum brasilense Sp7.

Authors:  S Moens; K Michiels; V Keijers; F Van Leuven; J Vanderleyden
Journal:  J Bacteriol       Date:  1995-10       Impact factor: 3.490

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