Kuhnke G, Theres C, Fritz H J, Ehring R
Institut für Genetik, Universität zu Köln, FRG.
EMBO J. 1989 Apr;8(4):1247-55. doi: 10.1002/j.1460-2075.1989.tb03498.x.
The Escherichia coli galactose operon contains an unusual array of closely spaced binding sites for proteins governing the expression from the two physically overlapping gal promoters. Based on studies of two gal promoter-up mutants we have previously suggested RNA-polymerase-induced DNA bending of gal promoter DNA. Here we present new evidence confirming and extending this interpretation. It was obtained by the circular permutation assay of gel electrophoretic mobility [Wu and Crothers (1984), Nature, 308, 509-513] applied to three analogous series of circularly permuted fragments derived from wild-type and two promoter-up mutant DNAs. The same circularly permuted DNA fragments have further been used to study the binding of gal repressor to its operator sites by electrophoretic mobility shift and by DNase I footprinting techniques. The main results are: (i) complexes carrying repressor either exclusively at the upstream operator O1 or at the downstream operator O2 exhibit different electrophoretic mobilities; (ii) binding to either one of the operators results in protein-induced DNA bending by the criteria of the circular permutation mobility assay; and (iii) occupation of both gal operators by gal repressor does not prevent cAMP-CRP-independent binding of RNA polymerase to the gal promoters, as judged by DNase I protection and gel retardation assays. The latter finding imposes constraints on any attempt to model the regulation of gal expression by assumed DNA-protein and protein-protein interactions.
大肠杆菌半乳糖操纵子包含一系列不同寻常的紧密排列的蛋白质结合位点,这些蛋白质控制着两个在物理上重叠的半乳糖启动子的表达。基于对两个半乳糖启动子上游突变体的研究,我们之前提出RNA聚合酶可诱导半乳糖启动子DNA发生弯曲。在此,我们提供新的证据来证实并扩展这一解释。证据来自凝胶电泳迁移率的环形置换分析[吴和克罗瑟斯(1984年),《自然》,308卷,509 - 513页],该分析应用于源自野生型和两个启动子上游突变体DNA的三个类似系列的环形置换片段。同样的环形置换DNA片段还被用于通过电泳迁移率变动分析和DNase I足迹分析技术研究半乳糖阻遏物与其操纵位点的结合。主要结果如下:(i)仅在上游操纵子O1或下游操纵子O2携带阻遏物的复合物表现出不同的电泳迁移率;(ii)根据环形置换迁移率分析的标准,与任一操纵子的结合都会导致蛋白质诱导的DNA弯曲;(iii)通过DNase I保护分析和凝胶阻滞分析判断,半乳糖阻遏物占据两个半乳糖操纵子并不妨碍RNA聚合酶与半乳糖启动子进行不依赖于cAMP - CRP的结合。后一发现对任何试图通过假定的DNA - 蛋白质和蛋白质 - 蛋白质相互作用来模拟半乳糖表达调控的尝试施加了限制。