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

机译:ppGpp和DksA对大肠杆菌RNA聚合酶-启动子复合物调控机制的新见解

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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.
机译:严格的响应调节剂四磷酸鸟苷(ppGpp)和蛋白DksA,结合RNA聚合酶(RNAP)并调节基因表达,以使细菌适应不同的环境条件。在这里,我们使用原子力显微镜和体外转录试验研究了这些调节剂对在rrnA P1,rrnB P1,其鉴别子(dis)和λpR上形成的开放启动子复合物(RPo)的构象和稳定性的影响。发起人。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包裹,其与UP元件的位置相关。调节剂的添加以启动子依赖性方式影响DNA包裹和RPO稳定性。总体而言,在ppGpp,DksA和起始核苷酸(iNTP)不同条件下获得的结果表明,ppGpp变构地阻止了与延长的DNA包装相关的构象变化,从而导致RPo稳定,而DksA直接干扰了核苷酸定位到RNAP活性位点中。在iNTPs敏感的rRNA启动子上,ppGpp和DksA显示出独立的抑制作用,而在iNTPs不敏感的pR启动子上,DksA根据其拮抗作用降低了ppGpp的作用。

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