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sigma factor mutations affecting the sequence-selective interaction of RNA polymerase with -10 region single-stranded DNA

机译:σ因子突变影响RNA聚合酶与-10区单链DNA的序列选择性相互作用

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Thesigmasubunit of RNA polymerase determines promoter recognition and catalyzes DNA strand separation. The -35 promoter region is recognized by a helix-turn-helix motif in region 4, while the -10 region is specified, at least in part, by an amphipathic helix in region 2. We have proposed that conserved aromatic residues insigmaregion 2.3 interact with the non-template strand of the -10 element to drive open complex formation. We now report that Bacillus subtilis sigmaA holoenzyme, but neither core nor sigmaA alone, binds with high selectivity to single-stranded (ss) DNA containing the non-template -10 consensus sequence. UV irradiation of holoenzyme-ssDNA complexes efficiently crosslinks sigmaA to DNA and protease mapping supports a primary contact site in or near region 2. Several mutations in sigmaA region 2.3, shown previously to impair promoter melting, affect ssDNA binding: Y184A decreases binding selectivity, while Y189A and W193A decrease the efficiency of photocrosslinking. These results support a model in which these aromatic amino acids are juxtaposed to ssDNA, consistent with their demonstrated role in stabilizing the open complex.
机译:RNA聚合酶的σ亚基决定启动子的识别并催化DNA链分离。 -35启动子区域在区域4中由螺旋-转-螺旋基序识别,而-10区域(至少部分地)在区域2中由两亲性螺旋指定。与-10元素的非模板链一起驱动开放复合物的形成。我们现在报告枯草芽孢杆菌sigmaA全酶,但既没有核心也不是sigmaA,以高选择性结合到含有非模板-10共有序列的单链(ss)DNA。紫外线对全酶-ssDNA复合物的照射可有效地使sigmaA交联至DNA,并且蛋白酶定位支持区域2或附近的主要接触位点。sigmaA 2.3区域中的一些突变(先前显示可削弱启动子融化,影响ssDNA结合):Y184A降低了结合选择性,而Y189A和W193A降低了光交联的效率。这些结果支持了一种模型,其中这些芳香族氨基酸与ssDNA并置,这与它们在稳定开放复合体中所显示的作用一致。

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