Huang X, Lopez de Saro F J, Helmann J D
Field of Biochemistry, Molecular and Cell Biology, Cornell University, Ithaca, NY 14853, USA.
Nucleic Acids Res. 1997 Jul 1;25(13):2603-9. doi: 10.1093/nar/25.13.2603.
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.
RNA聚合酶的σ亚基决定启动子识别并催化DNA链分离。-35启动子区域由区域4中的螺旋-转角-螺旋基序识别,而-10区域至少部分由区域2中的两亲性螺旋确定。我们曾提出,σ区域2.3中保守的芳香族残基与-10元件的非模板链相互作用以驱动开放复合物形成。我们现在报道,枯草芽孢杆菌σA全酶(而非单独的核心酶或σA)与含有非模板-10共有序列的单链(ss)DNA具有高选择性结合。全酶-ssDNA复合物的紫外线照射有效地使σA与DNA交联,蛋白酶图谱分析支持在区域2内或附近存在一个主要接触位点。σA区域2.3中先前显示会损害启动子解链的几个突变影响ssDNA结合:Y184A降低结合选择性,而Y189A和W193A降低光交联效率。这些结果支持一个模型,即这些芳香族氨基酸与ssDNA并列,这与其在稳定开放复合物中所起的作用一致。