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首页> 外文期刊>Nucleic Acids Research >RNA secondary structures regulate three steps of Rho-dependent transcription termination within a bacterial mRNA leader
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RNA secondary structures regulate three steps of Rho-dependent transcription termination within a bacterial mRNA leader

机译:RNA二级结构调节细菌mRNA领导者内的RHO依赖性转录终止的三个步骤

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摘要

Transcription termination events in bacteria often require the RNA helicase Rho. Typically, Rho promotes termination at the end of coding sequences, but it can also terminate transcription within leader regions to implement regulatory decisions. Rho-dependent termination requires initial recognition of a Rho utilization (rut) site on a nascent RNA by Rho's primary binding surface. However, it is presently unclear what factors determine the location of transcription termination, how RNA secondary structures influence this process and whether mechanistic differences distinguish constitutive from regulated Rho-dependent terminators. We previously demonstrated that the 5' leader mRNA of the Salmonella corA gene can adopt two mutually exclusive conformations that dictate accessibility of a rut site to Rho. We now report that the corA leader also controls two subsequent steps of Rho-dependent termination. First, the RNA conformation that presents an accessible rut site promotes pausing of RNA polymerase (RNAP) at a single Rho-dependent termination site over 100 nt downstream. Second, an additional RNA stem-loop promotes Rho activity and controls the location at which Rho-dependent termination occurs, despite having no effect on initial Rho binding to the corA leader. Thus, the multi-step nature of Rho-dependent termination may facilitate regulation of a given coding region by multiple cytoplasmic signals.
机译:细菌中的转录终止事件通常需要RNA螺旋酶Rho。通常,rhO在编码序列结束时促进终止,但它也可以终止领导区域内的转录来实施监管决策。依赖性终端需要通过RHO的主要结合表面初始识别Nascent RNA上的RHO利用率(RUT)位点。然而,目前尚不清楚因素决定转录终止的位置,RNA二级结构如何影响该过程以及机械差是否区分本构型来自受调节的RHO依赖性终端。我们之前证明了Salmonella Cora Gene的5'前导力MRNA可以采用两种相互排斥的构象,要求RUT现场的可达性与RHO。我们现在报告称Cora Leader还控制了依赖终止的两个后续步骤。首先,呈现可接近的RUT位点的RNA构象促进在下游100nt的单个RHO依赖性终止位点处的RNA聚合酶(RNAP)。其次,额外的RNA茎环促进RHO活性并控制依赖于依赖终止的位置,尽管对Cora领导的初始ROO结合没有影响。因此,RHO依赖性终止的多步性质可以通过多种细胞质信号促进给定的编码区域的调节。

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