大肠杆菌鞭毛主调控因子FlhD2C2对非鞭毛基因的结合及转录激活作用。

Binding and transcriptional activation of non-flagellar genes by the Escherichia coli flagellar master regulator FlhD2C2.

作者信息

Stafford Graham P, Ogi Tomoo, Hughes Colin

机构信息

University of Cambridge, Department of Pathology, Tennis Court Road, Cambridge CB2 1QP, UK.

Genome Damage and Stability Centre, University of Sussex, Science Park Road, Falmer, Brighton BN1 9QG, UK.

出版信息

Microbiology (Reading). 2005 Jun;151(Pt 6):1779-1788. doi: 10.1099/mic.0.27879-0.

Abstract

The gene hierarchy directing biogenesis of peritrichous flagella on the surface of Escherichia coli and other enterobacteria is controlled by the heterotetrameric master transcriptional regulator FlhD(2)C(2). To assess the extent to which FlhD(2)C(2) directly activates promoters of a wider regulon, a computational screen of the E. coli genome was used to search for gene-proximal DNA sequences similar to the 42-44 bp inverted repeat FlhD(2)C(2) binding consensus. This identified the binding sequences upstream of all eight flagella class II operons, and also putative novel FlhD(2)C(2) binding sites in the promoter regions of 39 non-flagellar genes. Nine representative non-flagellar promoter regions were all bound in vitro by active reconstituted FlhD(2)C(2) over the K(D) range 38-356 nM, and of the nine corresponding chromosomal promoter-lacZ fusions, those of the four genes b1904, b2446, wzz(fepE) and gltI showed up to 50-fold dependence on FlhD(2)C(2) in vivo. In comparison, four representative flagella class II promoters bound FlhD(2)C(2) in the K(D) range 12-43 nM and were upregulated in vivo 30- to 990-fold. The FlhD(2)C(2)-binding sites of the four regulated non-flagellar genes overlap by 1 or 2 bp the predicted -35 motif of the FlhD(2)C(2)-activated sigma(70) promoters, as is the case with FlhD(2)C(2)-dependent class II flagellar promoters. The data indicate a wider FlhD(2)C(2) regulon, in which non-flagellar genes are bound and activated directly, albeit less strongly, by the same mechanism as that regulating the flagella gene hierarchy.

摘要

指导大肠杆菌和其他肠道细菌表面周生鞭毛生物合成的基因层级由异源四聚体主转录调节因子FlhD(2)C(2)控制。为了评估FlhD(2)C(2)直接激活更广泛调控子启动子的程度,利用大肠杆菌基因组的计算筛选来搜索与42 - 44 bp反向重复FlhD(2)C(2)结合共有序列相似的基因近端DNA序列。这确定了所有八个鞭毛II类操纵子上游的结合序列,以及39个非鞭毛基因启动子区域中假定的新型FlhD(2)C(2)结合位点。九个代表性的非鞭毛启动子区域在体外均被活性重组的FlhD(2)C(2)结合,解离常数(K(D))范围为38 - 356 nM,在九个相应的染色体启动子 - lacZ融合体中,四个基因b1904、b2446、wzz(fepE)和gltI的融合体在体内对FlhD(2)C(2)的依赖性高达50倍。相比之下,四个代表性的鞭毛II类启动子在K(D)范围为12 - 43 nM时结合FlhD(2)C(2),并且在体内上调30至990倍。四个受调控的非鞭毛基因的FlhD(2)C(2)结合位点与FlhD(2)C(2)激活的σ(70)启动子的预测 - 35基序重叠1或2 bp,就像FlhD(2)C(2)依赖性II类鞭毛启动子的情况一样。数据表明存在更广泛的FlhD(2)C(2)调控子,其中非鞭毛基因通过与调节鞭毛基因层级相同的机制直接被结合并激活,尽管强度较低。

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