Lavigne M, Kolb A, Buc H
Institut Pasteur, Unité de Physicochimie des Macromolécules Biologiques (URA 1149 du CNRS), Paris, France.
Biochemistry. 1992 Oct 13;31(40):9647-56. doi: 10.1021/bi00155a018.
The cAMP-CRP complex activates the initiation of transcription at the Escherichia coli gal P1 promoter, and the activation efficiency is highly sensitive to the location of the complex on this promoter region. Moving the CRP binding site by one base pair toward the start of transcription significantly decreases the extent of activation in vivo and actually turns the cAMP-CRP complex into an inhibitor in in vitro experiments. A structural analysis of open complexes formed on the two promoter fragments at 37 degrees C has revealed three elements crucial for an optimal activation process: a strong upstream anchorage of RNA polymerase, a cooperative binding of CRP and RNA polymerase, and an accurate orientation of the two promoter regions located upstream and downstream of the CRP binding site. Furthermore, structural analysis of polymerase promoter complexes at lower temperatures suggests that RNA polymerase initially recognizes the upstream region of the gal P1 promoter and subsequently interacts with sequences from the -10 to +20 region to yield the final open complex structure. The involvement of CRP in these sequential events has been examined.
环磷酸腺苷 - 环磷酸腺苷受体蛋白(cAMP - CRP)复合物激活大肠杆菌半乳糖P1启动子处的转录起始,且激活效率对该复合物在启动子区域的位置高度敏感。将CRP结合位点向转录起始方向移动一个碱基对会显著降低体内的激活程度,并且在体外实验中实际上会使cAMP - CRP复合物变成抑制剂。在37摄氏度下对两个启动子片段形成的开放复合物进行的结构分析揭示了最佳激活过程的三个关键要素:RNA聚合酶的强上游锚定、CRP与RNA聚合酶的协同结合,以及位于CRP结合位点上游和下游的两个启动子区域的精确取向。此外,在较低温度下对聚合酶 - 启动子复合物的结构分析表明,RNA聚合酶最初识别半乳糖P1启动子的上游区域,随后与 - 10至 + 20区域的序列相互作用以产生最终的开放复合物结构。已经研究了CRP在这些连续事件中的参与情况。