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细菌鞭毛生物合成和群体游动的FlhD(2)C(2)转录主调控因子中各亚基的功能。

Functions of the subunits in the FlhD(2)C(2) transcriptional master regulator of bacterial flagellum biogenesis and swarming.

作者信息

Claret L, Hughes C

机构信息

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

出版信息

J Mol Biol. 2000 Nov 3;303(4):467-78. doi: 10.1006/jmbi.2000.4149.

Abstract

In enterobacteria like Salmonella, biogenesis of cell surface flagella needed for motility is dependent upon the master operon flhDC at the apex of the flagellar gene hierarchy. The operon products FlhD and FlhC act together in a FlhD(2)C(2 )heterotetramer to induce flagellar gene transcription, while FlhD also represses cell septation. The flhDC operon is pivotal to differentiation into elongated hyperflagellated swarm cells that undergo multicellular migration, most strikingly in Proteus. We set out to establish the mechanism of action of the FlhD(2)C(2) multimer. In Proteus swarm cell extracts, all the FlhC was assembled into the FlhD(2)C(2 )transcription activator, but FlhD additionally formed approximately equimolar amounts of a FlhD(2) homodimer. Both FlhD and FlhC subunits homodimerised in vivo and in vitro, suggesting that self-interactions stabilise the FlhD(2)C(2 )complex. The FlhC and FlhD subunit proteins were separately expressed and purified, and the FlhD(2)C(2)heterotetramer was reconstituted in vitro. Purified FlhC bound specifically and cooperatively to the promoter region of the flhDC-regulated flhB flagellar gene in the absence of FlhD. Purified FlhD was unable to bind this target DNA, but binding by the FlhD(2)C(2)complex was approximately tenfold greater than the FlhC subunit alone, suggesting that FlhD potentiated the FlhC/DNA interaction. In support of this possibility, pre-incubation of FlhC with FlhD reduced the apparent dissociation constant, K(D), for the FlhC/DNA complex from 100 nM to 13 nM. Furthermore, in competition assays, FlhD substantially increased the specificity of DNA recognition by FlhC, and also stabilised the resultant labile protein/DNA complex, prolonging its half-life from around two minutes to more than 40 minutes. FlhD(2)C(2)is therefore an atypical prokaryotic transcription activator in which interaction of the FlhC subunit with DNA target sequences is enhanced by the coexpressed helper subunit FlhD.

摘要

在诸如沙门氏菌这样的肠杆菌中,运动所需的细胞表面鞭毛的生物合成依赖于鞭毛基因层级顶端的主操纵子flhDC。操纵子产物FlhD和FlhC以FlhD(2)C(2)异源四聚体的形式共同作用,以诱导鞭毛基因转录,而FlhD也会抑制细胞分裂。flhDC操纵子对于分化成长丝状的多鞭毛群体细胞至关重要,这些细胞会进行多细胞迁移,在变形杆菌中最为显著。我们着手确定FlhD(2)C(2)多聚体的作用机制。在变形杆菌群体细胞提取物中,所有的FlhC都组装成了FlhD(2)C(2)转录激活因子,但FlhD还额外形成了约等摩尔量的FlhD(2)同型二聚体。FlhD和FlhC亚基在体内和体外都会形成同型二聚体,这表明自我相互作用稳定了FlhD(2)C(2)复合物。分别表达并纯化了FlhC和FlhD亚基蛋白,并在体外重构了FlhD(2)C(2)异源四聚体。在没有FlhD的情况下,纯化的FlhC能特异性且协同地结合flhDC调控的flhB鞭毛基因的启动子区域。纯化的FlhD无法结合该靶DNA,但FlhD(2)C(2)复合物的结合能力比单独的FlhC亚基大约高10倍,这表明FlhD增强了FlhC与DNA的相互作用。为支持这一可能性,将FlhC与FlhD预孵育可使FlhC/DNA复合物的表观解离常数K(D)从100 nM降至13 nM。此外,在竞争试验中,FlhD显著提高了FlhC对DNA识别的特异性,还稳定了由此产生的不稳定的蛋白质/DNA复合物,将其半衰期从约两分钟延长至40多分钟。因此,FlhD(2)C(2)是一种非典型的原核转录激活因子,其中FlhC亚基与DNA靶序列的相互作用因共表达的辅助亚基FlhD而增强。

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