Seyler R W, Moran C P
Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta GA 30322, USA.
Gene. 1996 Oct 24;177(1-2):129-32. doi: 10.1016/0378-1119(96)00288-0.
We used potassium permanganate (KMnO4) to identify unpaired thymidine (T) residues in promoter complexes formed by RNA polymerase (RNAP) associated with sigma E (sigma E-RNAP) from Bacillus subtilis. We found that a region of the spoIIID promoter from at least -10 to +1 becomes melted in the presence of this polymerase. In promoter complexes formed by RNAP associated with a mutant sigma E that melts promoter DNA inefficiently, we noted additional KMnO4 sensitivity at the -11 position of the spoIIID promoter. We suggest that the base pair at -11 is unpaired in both mutant and wild type (wt) complexes; however, close proximity of wt sigma E-RNAP with the T at -11 may protect it from KMnO4 attack. The absence of a close contact between the mutant sigma E-RNAP and the base at -11 may explain why this polymerase uses promoters less efficiently than wt sigma E-RNAP.
我们使用高锰酸钾(KMnO₄)来鉴定由来自枯草芽孢杆菌的与σE(σE-RNAP)相关的RNA聚合酶(RNAP)形成的启动子复合物中的未配对胸腺嘧啶(T)残基。我们发现,在这种聚合酶存在的情况下,spoIIID启动子至少从-10到+1的区域会发生解链。在由与一种突变型σE相关的RNAP形成的启动子复合物中,该突变型σE使启动子DNA解链效率低下,我们注意到spoIIID启动子的-11位对KMnO₄更敏感。我们认为,在突变体和野生型(wt)复合物中,-11位的碱基对都是未配对的;然而,wt σE-RNAP与-11位的T紧密接近可能会保护它免受KMnO₄的攻击。突变型σE-RNAP与-11位碱基之间缺乏紧密接触,这可能解释了为什么这种聚合酶使用启动子比wt σE-RNAP效率更低。