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PMID: 11929518 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Mutations in FlbD that relieve the dependency on flagellum assembly alter the temporal and spatial pattern of developmental transcription in Caulobacter crescentus.

Molecular microbiology ·Vol. 43 ·No. 3 ·2002-02-00 ·Pages 597-615

Muir RE, Gober JW

Abstract

The transcription factor FlbD regulates the temporal and spatial transcription of flagellar genes in the bacterium Caulobacter crescentus. Activation of FlbD requires cell cycle progression and the assembly of an early (class II) flagellum structure. In this report, we identify 20 independent gain-of-function mutations in flbD that relieve regulation by flagellar assembly. One of these, flbD-1204, contained a mutation in the receiver domain (V17M) and another, flbD-1231, in the DNA binding domain (V451G). Both of these mutations resulted in an aberrant pattern of cell cycle transcription. The presence of the FlbD-1204 allele also resulted in a loss of swarmer-pole-specific transcription. These results indicate that temporal and spatial transcription is influenced by the assembly of the nascent flagellar structure. The trans-acting positive and negative regulatory factor, FliX, couples flagellar assembly to the activation of FlbD and, as we show here, also influences temporal transcription. Furthermore, we show that FliX can suppress the activity of FlbD mutants that cannot be phosphorylated, and that FliX is required for FlbD stability, and vice versa. These results indicate that FliX may interact directly with FlbD to regulate its activity.

MeSH Terms
Amino Acid Sequence Bacterial Proteins/genetics,metabolism Caulobacter crescentus/genetics,physiology Cell Compartmentation/genetics DNA-Binding Proteins/genetics,metabolism Flagella/physiology Gene Expression Regulation, Bacterial Membrane Proteins/genetics,metabolism Molecular Sequence Data Mutation Sequence Homology, Amino Acid Transcription, Genetic
Chemicals
Bacterial Proteins DNA-Binding Proteins FlbD protein, Caulobacter crescentus FliX protein, Caulobacter crescentus Membrane Proteins
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Muir Rachel E
Department of Chemistry and Biochemistry, and Molecular Biology Institute, University of California, Los Angeles, CA 90095-1569, USA.
Gober James W
Article Info
Journal
Molecular microbiology
Abbr.
Mol Microbiol
ISSN
0950-382X
Published
2002-02-00
Pages
597-615
Language
English
Region
England
NLM ID
8712028
Subset
IM
Grants
NIGMS NIH HHS · GM07104 · United States
NIGMS NIH HHS · GM48417 · United States
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