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对ppGpp和DksA调控大肠杆菌RNA聚合酶-启动子复合物机制的新见解。

New insights into the regulatory mechanisms of ppGpp and DksA on Escherichia coli RNA polymerase-promoter complex.

作者信息

Doniselli Nicola, Rodriguez-Aliaga Piere, Amidani Davide, Bardales Jorge A, Bustamante Carlos, Guerra Daniel G, Rivetti Claudio

机构信息

Dipartimento di Bioscienze, Università degli Studi di Parma, Parma, Italy.

Jason L. Choy Laboratory of Single Molecule Biophysics, University of California, Berkeley, CA, USA Biophysics Graduate Group, University of California, Berkeley, CA, USA Laboratorio de Moléculas Individuales, Facultad de Ciencias y Filosofía, Universidad Peruana Cayetano Heredia, Av Honorio Delgado 430, San Martin de Porras, Lima-31, Peru.

出版信息

Nucleic Acids Res. 2015 May 26;43(10):5249-62. doi: 10.1093/nar/gkv391. Epub 2015 Apr 27.

Abstract

The stringent response modulators, guanosine tetraphosphate (ppGpp) and protein DksA, bind RNA polymerase (RNAP) and regulate gene expression to adapt bacteria to different environmental conditions. Here, we use Atomic Force Microscopy and in vitro transcription assays to study the effects of these modulators on the conformation and stability of the open promoter complex (RPo) formed at the rrnA P1, rrnB P1, its discriminator (dis) variant and λ pR promoters. In the absence of modulators, RPo formed at these promoters show different extents of DNA wrapping which correlate with the position of UP elements. Addition of the modulators affects both DNA wrapping and RPo stability in a promoter-dependent manner. Overall, the results obtained under different conditions of ppGpp, DksA and initiating nucleotides (iNTPs) indicate that ppGpp allosterically prevents the conformational changes associated with an extended DNA wrapping that leads to RPo stabilization, while DksA interferes directly with nucleotide positioning into the RNAP active site. At the iNTPs-sensitive rRNA promoters ppGpp and DksA display an independent inhibitory effect, while at the iNTPs-insensitive pR promoter DksA reduces the effect of ppGpp in accordance with their antagonistic role.

摘要

严格反应调节剂鸟苷四磷酸(ppGpp)和蛋白质DksA与RNA聚合酶(RNAP)结合,并调节基因表达,以使细菌适应不同的环境条件。在此,我们使用原子力显微镜和体外转录分析来研究这些调节剂对在rrnA P1、rrnB P1、其鉴别子(dis)变体和λ pR启动子处形成的开放启动子复合物(RPo)的构象和稳定性的影响。在没有调节剂的情况下,在这些启动子处形成的RPo显示出不同程度的DNA缠绕,这与上游元件的位置相关。添加调节剂以启动子依赖的方式影响DNA缠绕和RPo稳定性。总体而言,在ppGpp、DksA和起始核苷酸(iNTPs)的不同条件下获得的结果表明,ppGpp变构地阻止与导致RPo稳定的扩展DNA缠绕相关的构象变化,而DksA直接干扰核苷酸定位到RNAP活性位点。在对iNTPs敏感的rRNA启动子处,ppGpp和DksA表现出独立的抑制作用,而在对iNTPs不敏感的pR启动子处,DksA根据它们的拮抗作用降低了ppGpp的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd60/4446441/47cbaf4eada4/gkv391fig1.jpg

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