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PMID: 1847367 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Timing of flagellar gene expression in the Caulobacter cell cycle is determined by a transcriptional cascade of positive regulatory genes.

Journal of bacteriology ·Vol. 173 ·No. 4 ·1991-02-00 ·Pages 1514-22

Ohta N, Chen LS, Mullin DA, Newton A

Abstract

The Caulobacter crescentus flagellar (fla) genes are organized in a regulatory hierarchy in which genes at each level are required for expression of those at the next lower level. To determine the role of this hierarchy in the timing of fla gene expression, we have examined the organization and cell cycle regulation of genes located in the hook gene cluster. As shown here, this cluster is organized into four multicistronic transcription units flaN, flbG, flaO, and flbF that contain fla genes plus a fifth transcription unit II.1 of unknown function. Transcription unit II.1 is regulated independently of the fla gene hierarchy, and it is expressed with a unique pattern of periodicity very late in the cell cycle. The flaN, flbG, and flaO operons are all transcribed periodically, and flaO, which is near the top of the hierarchy and required in trans for the activation of flaN and flbG operons, is expressed earlier in the cell cycle than the other two transcription units. We have shown that delaying flaO transcription by fusing it to the II.1 promoter also delayed the subsequent expression of the flbG operon and the 27- and 25-kDa flagellin genes that are at the bottom of the regulatory hierarchy. Thus, the sequence and timing of fla gene expression in the cell cycle are determined in large measure by the positions of these genes in the regulatory hierarchy. These results also suggest that periodic transcription is a general feature of fla gene expression in C. crescentus.

MeSH Terms
Bacterial Proteins/biosynthesis Cell Cycle/physiology DNA Probes Flagellin/biosynthesis Gene Expression Regulation, Bacterial Genes, Regulator/physiology Repressor Proteins/biosynthesis Restriction Mapping Transcription, Genetic beta-Galactosidase/metabolism
Chemicals
Bacterial Proteins DNA Probes Repressor Proteins hook protein, bacterial flagellum Flagellin beta-Galactosidase
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Ohta N
Department of Molecular Biology, Lewis Thomas Laboratory, Princeton University, New Jersey 08544-1014.
Chen L S
Mullin D A
Newton A
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39 references, click to expand
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Article Info
Journal
Journal of bacteriology
Abbr.
J Bacteriol
ISSN
0021-9193
Published
1991-02-00
Pages
1514-22
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC207290
Subset
IM
Grants
NIGMS NIH HHS · 5 T32 GM07388 · United States
NCI NIH HHS · CA09528 · United States
NIGMS NIH HHS · GM 22299 · United States
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