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Promoter recognition by Escherichia coli RNA polymerase: Effects of the UP element on open complex formation and promoter clearance

机译:大肠杆菌RNA聚合酶对启动子的识别:UP元件对开放复合物形成和启动子清除的影响

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摘要

Escherichia coli promoters for transcription of ribosomal and tRNAs are greatly activated by an A+T-rich "UP" element upstream of the -35 region. These same promoters have also been found to otherwise deviate in several respects from the consensus promoter sequence. Here we present the results of a kinetic characterization of the interaction of Escherichia coli RNA polymerase with UP element-containing promoters which by virtue of consensus or near-consensus sequence features should be among the most optimal that can be encountered by Escherichia coli RNA polymerase. We show that fur such promoters, (1) the second-order rate constant describing formation of the initial (closed) complex is close to that expected for a diffusion-limited process, (2) the extent of activation by the UP clement is temperature-sensitive, (3) the UP element accelerates a process after DNA binding by RNA polymerase, and (4) the presence of the UP element delays promoter clearance upon addition of nucleoside triphosphates to preformed RNA polymerase-promoter complexes. Finally, we provide evidence in support of models which describe the DNA melting process accompanying open complex formation as initiating in the -10 promoter region and progressing in the downstream direction. [References: 30]
机译:用于转录核糖体和tRNA的大肠杆菌启动子被-35区上游富含A + T的“ UP”元件极大地激活。还发现这些相同的启动子在某些方面与共有启动子序列不同。在这里,我们介绍了大肠杆菌RNA聚合酶与含UP元素的启动子相互作用的动力学表征的结果,借助于共有或接近共识的序列特征,应该是大肠杆菌RNA聚合酶可以遇到的最理想的启动子。我们显示了这类启动子,(1)描述初始(封闭)复合物形成的二级速率常数接近于扩散受限过程的预期,(2)UP元素的活化程度是温度敏感性,(3)UP元件加速了RNA聚合酶与DNA结合后的过程,并且(4)UP元件的存在在将核苷三磷酸添加到预先形成的RNA聚合酶-启动子复合物中后延迟了启动子清除。最后,我们提供了支持模型的证据,这些模型描述了伴随着开放复合物形成的DNA融化过程,该过程开始于-10启动子区域并向下游方向发展。 [参考:30]

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