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RNA polymerase alpha subunit binding site in positively controlled promoters: a new model for RNA polymerase-promoter interaction and transcriptional activation in the Escherichia coli ada and aidB genes

机译:阳性对照启动子中RNa聚合酶α亚基结合位点:大肠杆菌ada和aidB基因中RNa聚合酶启动子相互作用和转录激活的新模型

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摘要

The ada and aidB genes are part of the adaptive response to DNA methylation damage in Escherichia coli. Transcription of the ada and the aidB genes is triggered by binding of the methylated Ada protein (meAda) to a specific sequence located 40-60 base pairs upstream of the transcriptional start, which is internal to an A/T-rich region. In this report we demonstrate that the Ada binding site is also a binding site for RNA polymerase. RNA polymerase is able to bind the -40 to -60 region of the ada and the aidB promoters in the absence of meAda, and its binding is mediated by the alpha subunit. This region resembles the UP element of the rrnB P1 promoter in location, sequence and mechanism of interaction with RNA polymerase. We discuss the function of UP-like elements in positively controlled promoters and provide evidence that Ada does not act by enhancing RNA polymerase binding affinity to the promoter region. Instead, Ada stimulates transcription by modifying the nature of the RNA polymerase-promoter interaction, allowing RNA polymerase to recognize the core promoter -35 and -10 elements in addition to the UP-like element.
机译:ada和aidB基因是大肠杆菌对DNA甲基化损伤的适应性反应的一部分。通过将甲基化的Ada蛋白(meAda)与位于转录起始位点上游40-60个碱基对的特定序列结合来触发ada和aidB基因的转录,该序列位于富含A / T的区域内。在此报告中,我们证明了Ada结合位点也是RNA聚合酶的结合位点。在没有meAda的情况下,RNA聚合酶能够结合ada和aidB启动子的-40至-60区,并且其结合是由α亚基介导的。该区域在位置,序列和与RNA聚合酶相互作用的机制上类似于rrnB P1启动子的UP元件。我们讨论了UP样元件在正调控启动子中的功能,并提供了Ada不能通过增强RNA聚合酶对启动子区域的亲和力来发挥作用的证据。取而代之的是,Ada通过修饰RNA聚合酶与启动子相互作用的性质来刺激转录,从而使RNA聚合酶除了识别UP样元件外,还识别核心启动子-35和-10元件。

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