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Genetics and Molecular Biology |
Department of Biochemistry, Imperial College of Science, Technology and Medicine, London SW7 2AY, UK1
Author for correspondence: M. R. K. Alley. Tel: +44 20 7594 5304. Fax: +44 20 7594 5207. e-mail: d.alley{at}ic.ac.uk
The Caulobacter crescentus che promoter region consists of two divergent promoters, directing expression of the major chemotaxis operon and a novel gene cagA (chemotaxis associated gene A). Analyses of start sites by primer extension and alignment of the divergent promoters revealed significant similarities between them at the -35 promoter region. Both mcpA and cagA are differentially expressed in the cell cycle, with maximal activation of transcription in predivisional cells. The main difference between the mcpA and cagA promoters is that, in common with the fljK flagellin, cagA is expressed in swarmer cells. A cagAlacZ promoter fusion that contains 36 bases of untranslated mRNA has sufficient information to segregate the lacZ transcript to swarmer cells. Expression of mcpA and cagA was dependent on DNA replication. Transcriptional epistasis experiments were performed to identify potential regulators in the flagellar hierarchy. The sigma factor RpoN, which is required for flagellar biogenesis, is not required for mcpA and cagA expression. Mutations in the genes for the MS-ring and the switch complex (flagellar class II mutants) do not affect expression of mcpA and cagA. However, CtrA, an essential response regulator of flagellar gene transcription, is required.
Keywords: cell cycle, Caulobacter crescentus, transcriptional regulation, flagella
Abbreviations: HU, hydroxyurea
a Present address: Department of Biology, Imperial College of Science, Technology and Medicine, London SW7 2AY, UK.
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