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幽门螺杆菌的运动性由转录激活因子FlgR协同调节,FlgR是一种NtrC同源物。

Motility of Helicobacter pylori is coordinately regulated by the transcriptional activator FlgR, an NtrC homolog.

作者信息

Spohn G, Scarlato V

机构信息

Department of Molecular Biology, Chiron SpA, 53100 Siena, Italy.

出版信息

J Bacteriol. 1999 Jan;181(2):593-9. doi: 10.1128/JB.181.2.593-599.1999.

Abstract

sigma54 is the subunit of bacterial RNA polymerase that transcribes from promoters with enhancer elements bound by enhancer-binding proteins. By computer searches of Helicobacter pylori genomic sequences, chromosomal gene disruption, and RNA analyses, we have identified sigma54-recognized promoters that regulate transcription of flagellar basal body and hook genes, as well as the enhancer-binding protein FlgR (flagellum regulator), a transactivating protein of the NtrC family. We demonstrate that FlgR is required for bacterial motility and transcription of five promoters for seven basal body and hook genes. In addition, FlgR acts as a repressor of transcription of the sigma28-regulated flaA flagellin gene promoter, while changes in DNA topology repress transcription of the sigma54-regulated flaB flagellin gene promoter. Our data indicate that regulation of flagellar gene expression in H. pylori shows similarities with that in enterobacteriaceae and Caulobacter.

摘要

σ54是细菌RNA聚合酶的亚基,它从与增强子结合蛋白结合的具有增强子元件的启动子进行转录。通过对幽门螺杆菌基因组序列的计算机搜索、染色体基因破坏和RNA分析,我们鉴定出了σ54识别的启动子,这些启动子调节鞭毛基体和钩形基因的转录,以及增强子结合蛋白FlgR(鞭毛调节因子),它是NtrC家族的一种反式激活蛋白。我们证明,FlgR对于细菌运动以及七个基体和钩形基因的五个启动子的转录是必需的。此外,FlgR作为σ28调节的flaA鞭毛蛋白基因启动子转录的阻遏物,而DNA拓扑结构的变化则抑制σ54调节的flaB鞭毛蛋白基因启动子的转录。我们的数据表明,幽门螺杆菌中鞭毛基因表达的调控与肠杆菌科和柄杆菌中的调控有相似之处。

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