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枯草芽孢杆菌应答调节因子Spo0A通过修饰RNA聚合酶启动子复合物来刺激spoIIG操纵子的转录。

The Bacillus subtilis response regulator Spo0A stimulates transcription of the spoIIG operon through modification of RNA polymerase promoter complexes.

作者信息

Bird T H, Grimsley J K, Hoch J A, Spiegelman G B

机构信息

Department of Molecular and Experimental Medicine, Research Institute of Scripps Clinic, La Jolla, CA 92037, USA.

出版信息

J Mol Biol. 1996 Mar 1;256(3):436-48. doi: 10.1006/jmbi.1996.0099.

Abstract

Sporulation in Bacillus subtilis is dependent on the response regulator Spo0A, which both represses and activates transcription in vitro. The activity of Spo0A is increased by phosphorylation. We previously demonstrated that the phosphorylation increased the ability of Spo0A to stimulate in vivo transcription from the promoter for the spoIIG operon, one of the operons known to be regulated by Spo0A in vivo. In the work reported here we have examined the kinetics of transcription initiation at the spoIIG operon promoter using a single round transcription assay and the kinetics of formation of spoIIG promoter-RNA polymerase complexes using DNase I footprinting. Both the kinetic assays and the footprint assays indicated that the initial binding of the polymerase to the template was not dependent on the presence of Spo0A. The phosphorylated form of Spo0A stimulated the rate of initiation by affecting a step that occurred after the initial interaction of the polymerase with the template. Phosphorylation of Spo0A may stimulate transcription by modifying preinitiation complexes containing the polymerase and the promoter.

摘要

枯草芽孢杆菌中的孢子形成依赖于应答调节因子Spo0A,它在体外既能抑制转录又能激活转录。Spo0A的活性通过磷酸化作用增强。我们之前证明,磷酸化作用增强了Spo0A在体内刺激spoIIG操纵子启动子转录的能力,spoIIG操纵子是已知在体内受Spo0A调控的操纵子之一。在本文报道的工作中,我们使用单轮转录分析研究了spoIIG操纵子启动子处转录起始的动力学,并使用DNase I足迹法研究了spoIIG启动子 - RNA聚合酶复合物形成的动力学。动力学分析和足迹分析均表明,聚合酶与模板的初始结合不依赖于Spo0A的存在。磷酸化形式的Spo0A通过影响聚合酶与模板初始相互作用之后发生的一个步骤来刺激起始速率。Spo0A的磷酸化可能通过修饰包含聚合酶和启动子的起始前复合物来刺激转录。

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