Attey A, Belyaeva T, Savery N, Hoggett J, Fujita N, Ishihama A, Busby S
School of Biochemistry, University of Birmingham, UK.
Nucleic Acids Res. 1994 Oct 25;22(21):4375-80. doi: 10.1093/nar/22.21.4375.
DNAase I footprinting has been used to study open complexes between Escherichia coli RNA polymerase and the galactose operon P1 promoter, both in the absence and the presence of CRP (the cyclic AMP receptor protein, a transcription activator). From the effects of deletion of the C-terminal part of the RNA polymerase alpha subunit, we deduce that alpha binds at the upstream end of both the binary RNA polymerase-galP1 and ternary RNA polymerase-CRP-galP1 complexes. Disruption of the alpha-upstream contact suppresses open complex formation at galP1 at lower temperatures. In ternary RNA polymerase-CRP-galP1 complexes, alpha appears to make direct contact with Activating Region 1 in CRP. DNAase I footprinting has been used to detect and quantify interactions between purified alpha and CRP bound at galP1.
DNA酶I足迹法已被用于研究大肠杆菌RNA聚合酶与半乳糖操纵子P1启动子之间的开放复合物,包括在不存在和存在CRP(环磷酸腺苷受体蛋白,一种转录激活因子)的情况下。从RNA聚合酶α亚基C末端部分缺失的影响,我们推断α在二元RNA聚合酶-galP1和三元RNA聚合酶-CRP-galP1复合物的上游末端结合。α与上游的接触中断会抑制在较低温度下galP1处开放复合物的形成。在三元RNA聚合酶-CRP-galP1复合物中,α似乎与CRP中的激活区域1直接接触。DNA酶I足迹法已被用于检测和定量在galP1处结合的纯化α与CRP之间的相互作用。