Literature DB >> 7814323

Caulobacter FliQ and FliR membrane proteins, required for flagellar biogenesis and cell division, belong to a family of virulence factor export proteins.

W Y Zhuang1, L Shapiro.   

Abstract

The Caulobacter crescentus fliQ and fliR genes encode membrane proteins that have a role in an early step of flagellar biogenesis and belong to a family of proteins implicated in the export of virulence factors. These include the MopD and MopE proteins from Erwinia carotovora, the Spa9 and Spa29 proteins from Shigella flexneri, and the YscS protein from Yersinia pestis. Inclusion in this family of proteins suggests that FliQ and FliR may participate in an export pathway required for flagellum assembly. In addition, mutations in either fliQ or fliR exhibit defects in cell division and thus may participate directly or indirectly in the division process. fliQ and fliR are class II flagellar genes residing near the top of the regulatory hierarchy that determines the order of flagellar gene transcription. The promoter sequence of the fliQR operon differs from most known bacterial promoter sequences but is similar to other Caulobacter class II flagellar gene promoter sequences. The conserved nucleotides in the promoter region are clustered in the -10, -20 to -30, and -35 regions. The importance of the conserved bases for promoter activity was demonstrated by mutational analysis. Transcription of the fliQR operon is initiated at a specific time in the cell cycle, and deletion analysis revealed that the minimal sequence required for transcriptional activation resides within 59 bp of the start site.

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Year:  1995        PMID: 7814323      PMCID: PMC176597          DOI: 10.1128/jb.177.2.343-356.1995

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


  58 in total

1.  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

2.  Export of an N-terminal fragment of Escherichia coli flagellin by a flagellum-specific pathway.

Authors:  G Kuwajima; I Kawagishi; M Homma; J Asaka; E Kondo; R M Macnab
Journal:  Proc Natl Acad Sci U S A       Date:  1989-07       Impact factor: 11.205

3.  Structure of the core and central channel of bacterial flagella.

Authors:  K Namba; I Yamashita; F Vonderviszt
Journal:  Nature       Date:  1989-12-07       Impact factor: 49.962

4.  Morphological pathway of flagellar assembly in Salmonella typhimurium.

Authors:  T Kubori; N Shimamoto; S Yamaguchi; K Namba; S Aizawa
Journal:  J Mol Biol       Date:  1992-07-20       Impact factor: 5.469

5.  Nucleotide sequences of Bacillus subtilis flagellar biosynthetic genes fliP and fliQ and identification of a novel flagellar gene, fliZ.

Authors:  D S Bischoff; M D Weinreich; G W Ordal
Journal:  J Bacteriol       Date:  1992-06       Impact factor: 3.490

6.  L-, P-, and M-ring proteins of the flagellar basal body of Salmonella typhimurium: gene sequences and deduced protein sequences.

Authors:  C J Jones; M Homma; R M Macnab
Journal:  J Bacteriol       Date:  1989-07       Impact factor: 3.490

7.  Transmission electron microscopy and immunocytochemical studies of yeast: analysis of HMG-CoA reductase overproduction by electron microscopy.

Authors:  R Wright; J Rine
Journal:  Methods Cell Biol       Date:  1989       Impact factor: 1.441

8.  Genetic switching in the flagellar gene hierarchy of Caulobacter requires negative as well as positive regulation of transcription.

Authors:  A Newton; N Ohta; G Ramakrishnan; D Mullin; G Raymond
Journal:  Proc Natl Acad Sci U S A       Date:  1989-09       Impact factor: 11.205

9.  Negative transcriptional regulation in the Caulobacter flagellar hierarchy.

Authors:  H Xu; A Dingwall; L Shapiro
Journal:  Proc Natl Acad Sci U S A       Date:  1989-09       Impact factor: 11.205

10.  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

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  24 in total

1.  A family of six flagellin genes contributes to the Caulobacter crescentus flagellar filament.

Authors:  B Ely; T W Ely; W B Crymes; S A Minnich
Journal:  J Bacteriol       Date:  2000-09       Impact factor: 3.490

2.  Molecular characterization of a flagellar export locus of Helicobacter pylori.

Authors:  S Porwollik; B Noonan; P W O'Toole
Journal:  Infect Immun       Date:  1999-05       Impact factor: 3.441

Review 3.  Complex regulatory pathways coordinate cell-cycle progression and development in Caulobacter crescentus.

Authors:  Pamela J B Brown; Gail G Hardy; Michael J Trimble; Yves V Brun
Journal:  Adv Microb Physiol       Date:  2009       Impact factor: 3.517

4.  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

5.  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

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.  An essential, multicomponent signal transduction pathway required for cell cycle regulation in Caulobacter.

Authors:  J Wu; N Ohta; A Newton
Journal:  Proc Natl Acad Sci U S A       Date:  1998-02-17       Impact factor: 11.205

8.  A mutation that uncouples flagellum assembly from transcription alters the temporal pattern of flagellar gene expression in Caulobacter crescentus.

Authors:  E K Mangan; M Bartamian; J W Gober
Journal:  J Bacteriol       Date:  1995-06       Impact factor: 3.490

9.  Flagellar assembly in Caulobacter crescentus: a basal body P-ring null mutation affects stability of the L-ring protein.

Authors:  C D Mohr; U Jenal; L Shapiro
Journal:  J Bacteriol       Date:  1996-02       Impact factor: 3.490

10.  Conserved gene cluster at replication origins of the alpha-proteobacteria Caulobacter crescentus and Rickettsia prowazekii.

Authors:  A K Brassinga; R Siam; G T Marczynski
Journal:  J Bacteriol       Date:  2001-03       Impact factor: 3.490

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