Hofer B, Müller D, Köster H
Institut für Organische Chemie und Biochemie der Universität Hamburg, F.R.G.
Biochim Biophys Acta. 1987 Dec 8;910(3):254-60. doi: 10.1016/0167-4781(87)90118-7.
A 302 bp DNA fragment and a 113 bp subfragment of the former, both containing the fd gene VIII promoter (P VIII), were found to exhibit temperature-dependent differential behaviour in RNA chain initiation from P VIII. At 37 degrees C no significant differences were observed, while at 17 degrees C chain initiation was strongly suppressed only with the 113 bp fragment. This phenomenon depended on the presence of the (blunt) DNA terminus upstream from P VIII (position -70). Footprinting revealed that at 17 degrees C RNA polymerase was bound to this DNA fragment in a different mode. Contacts were observed only upstream from position -25. On the contrary, at 37 degrees C only the promoter complex footprint was visible. These results indicate that at 17 degrees C formation of the non-initiating complex is more favourable than formation of the promoter complex (which is closed at 17 degrees C; Hofer, B., Müller, D. and Köster, H. (1985) Nucleic Acids Res. 13, 5995-6013) and that formation of both complexes is mutually exclusive. No footprints of RNA polymerase were observed at other DNA termini. This indicates a sequence-specificity for the interaction at the terminus of the 113 bp fragment. The footprint pattern, together with features of the DNA sequence, suggests that the contacts involved in this interaction are similar to those promoter contacts formed upstream from position -20 and that DNA without a -10 region can be specifically recognized by RNA polymerase.
发现一个302 bp的DNA片段及其113 bp的亚片段(二者均含有fd基因VIII启动子(P VIII))在从P VIII起始RNA链时呈现出温度依赖性差异行为。在37℃时未观察到显著差异,而在17℃时,只有113 bp的片段强烈抑制链起始。这种现象取决于P VIII上游(-70位)(平端)DNA末端的存在。足迹分析显示,在17℃时,RNA聚合酶以不同模式与该DNA片段结合。仅在-25位上游观察到接触。相反,在37℃时,仅可见启动子复合物足迹。这些结果表明,在17℃时,非起始复合物的形成比启动子复合物(在17℃时是封闭的;霍费尔,B.,米勒,D.和克斯特,H.(1985年)《核酸研究》13,5995 - 6013)的形成更有利,并且两种复合物的形成是相互排斥的。在其他DNA末端未观察到RNA聚合酶的足迹。这表明在113 bp片段末端的相互作用具有序列特异性。足迹模式以及DNA序列特征表明,这种相互作用中涉及的接触类似于在-20位上游形成的启动子接触,并且没有-10区域的DNA可以被RNA聚合酶特异性识别。