Previous Article | Next Article ![]()
Journal of Bacteriology, January 2001, p. 725-735, Vol. 183, No. 2
Department of Chemistry and Biochemistry and
the Molecular Biology Institute, University of California at Los
Angeles, Los Angeles, California 90095-1569
Received 14 June 2000/Accepted 31 October 2000
The gram-negative bacterium Caulobacter crescentus has
a life cycle that includes two distinct and separable developmental stages, a motile swarmer phase and a sessile stalked phase. The cell
cycle-controlled biogenesis of the single polar flagellum of the
swarmer cell is the best-studied aspect of this developmental program.
The flagellar regulon is arranged into a rigid trans-acting hierarchy of gene expression in which successful expression of early genes is required for the expression of genes that are later in
the hierarchy and in which the order of gene expression mirrors the
order of assembly of gene products into the completed flagellum. The
flgBC-fliE genes were identified as a result of
the C. crescentus genome sequencing project and encode the
homologues of two flagellar proximal rod proteins, FlgB and FlgC, and
one conserved protein, FliE, that is of unknown function. Footprint
assays on a DNA fragment containing the operon promoter as well as in
vivo mutant suppressor analysis of promoter mutations indicate that
this operon is controlled by the cell cycle response regulator CtrA,
which with
0021-9193/01/$04.00+0 DOI: 10.1128/JB.183.2.725-735.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Temporal Regulation of Genes Encoding the
Flagellar Proximal Rod in Caulobacter
crescentus
70 is responsible for regulating
transcription of other early flagellar genes in C. crescentus. Promoter analysis, timing of expression, and
epistasis experiments place these genes outside of the flagellar regulatory hierarchy; they are expressed in class II mutants, and
flgB deletions do not prevent class III gene expression.
This operon is also unusual in that it is expressed from a promoter that is divergent from the class II operon containing fliP,
which encodes a member of the flagellum-specific protein export apparatus.
*
Corresponding author. Mailing address: Department of
Chemistry and Biochemistry and the Molecular Biology Institute,
University of California at Los Angeles, Los Angeles, CA 90095-1569. Phone: (310) 206-9440. Fax: (310) 206-5213. E-mail:
gober{at}chem.ucla.edu.
This article has been cited by other articles:
Copyright © 2009 by the American Society for Microbiology. For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»