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J. Bacteriol., Jul 1995, 3656-3667, Vol 177, No. 13
JW Gober, CH Boyd, M Jarvis, EK Mangan, MF Rizzo and JA Wingrove
In Caulobacter crescentus, the genes encoding a single polar flagellum are
expressed under cell cycle control. In this report, we describe the
characterization of two early class II flagellar genes contained in the
orfX-fliP locus. Strains containing mutations in this locus exhibit a
filamentous growth phenotype and fail to express class III and IV flagellar
genes. A complementing DNA fragment was sequenced and found to contain two
potential open reading frames. The first, orfX, is predicted to encode a
105-amino-acid polypeptide that is similar to MopB, a protein which is
required for both motility and virulence in Erwinia carotovora. The deduced
amino acid sequence of the second open reading frame, fliP, is 264 amino
acids in length and shows significant sequence identity with the FliP
protein of Escherichia coli as well as virulence proteins of several plant
and mammalian pathogens. The FliP homolog in pathogenic organisms has been
implicated in the secretion of virulence factors, suggesting that the
export of virulence proteins and some flagellar proteins share a common
mechanism. The 5' end of orfX- fliP mRNA was determined and revealed an
upstream promoter sequence that shares few conserved features with that of
other early Caulobacter flagellar genes, suggesting that transcription of
orfX-fliP may require a different complement of trans-acting factors. In C.
crescentus, orfX- fliP is transcribed under cell cycle control, with a peak
of transcriptional activity in the middle portion of the cell cycle. Later
in the cell cycle, orfX-fliP expression occurs in both poles of the
predivisional cell. Protein fusions to a lacZ reporter gene indicate that
FliP is specifically targeted to the swarmer compartment of the
predivisional cell.
Copyright © 1995, American Society for Microbiology
Temporal and spatial regulation of fliP, an early flagellar gene of Caulobacter crescentus that is required for motility and normal cell division
Department of Chemistry and Biochemistry, University of California, Los Angeles 90095-1569, USA.
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