ArticleJournal of bacteriology1994
Multiple structural proteins are required for both transcriptional activation and negative autoregulation of Caulobacter crescentus flagellar genes.
Article in Journal of bacteriology, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.
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Who cites it
24 citing papers in PubMed, 67 citations in OpenAlex.
- Phosphatase to kinase switch of a critical enzyme contributes to timing of cell differentiation.mBio · 2024Article
- Phase separation modulates the assembly and dynamics of a polarity-related scaffold-signaling hub.Nature communications · 2022Article
- Article
- Functional Activation of the Flagellar Type III Secretion Export Apparatus.PLoS genetics · 2015Article
- Direct interaction of FliX and FlbD is required for their regulatory activity in Caulobacter crescentus.BMC microbiology · 2011Article
- Role of the cytoplasmic C terminus of the FliF motor protein in flagellar assembly and rotation.Journal of bacteriology · 2003Article
- Intergenic suppression between the flagellar MS ring protein FliF of Salmonella and FlhA, a membrane component of its export apparatus.Journal of bacteriology · 2001Article
- fleN, a gene that regulates flagellar number in Pseudomonas aeruginosa.Journal of bacteriology · 2000Article
- FlbT couples flagellum assembly to gene expression in Caulobacter crescentus.Journal of bacteriology · 1999Article
- Regulated expression of a highly conserved regulatory gene cluster is necessary for controlling photosynthesis gene expression in response to anaerobiosis in Rhodobacter capsulatus.Journal of bacteriology · 1999Article
- An extreme clockwise switch bias mutation in fliG of Salmonella typhimurium and its suppression by slow-motile mutations in motA and motB.Journal of bacteriology · 1997Article
- Posttranscriptional regulation of Caulobacter flagellin genes by a late flagellum assembly checkpoint.Journal of bacteriology · 1997Article
- The hrpA and hrpC operons of Erwinia amylovora encode components of a type III pathway that secretes harpin.Journal of bacteriology · 1997Article
- Isolation and characterization of a xylose-dependent promoter from Caulobacter crescentus.Journal of bacteriology · 1997Article
- Cell cycle-controlled proteolysis of a flagellar motor protein that is asymmetrically distributed in the Caulobacter predivisional cell.The EMBO journal · 1996Article
- Erwinia amylovora secretes harpin via a type III pathway and contains a homolog of yopN of Yersinia spp.Journal of bacteriology · 1996Article
- A cell cycle-regulated bacterial DNA methyltransferase is essential for viability.Proceedings of the National Academy of Sciences of the United States of America · 1996Article
- Cloning and phenotypic characterization of fleS and fleR, new response regulators of Pseudomonas aeruginosa which regulate motility and adhesion to mucin.Infection and immunity · 1995Article
- Cloning, sequencing, and phenotypic analysis of laf1, encoding the flagellin of the lateral flagella of Azospirillum brasilense Sp7.Journal of bacteriology · 1995Article
- Temporal and spatial regulation of fliP, an early flagellar gene of Caulobacter crescentus that is required for motility and normal cell division.Journal of bacteriology · 1995Article
Corrections and comments
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Authors and funding
3 authors at 1 institution in 1 country.
Funding
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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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.