首页> 美国卫生研究院文献>The EMBO Journal >Unusual properties of promoter-up mutations in the Escherichia coli galactose operon and evidence suggesting RNA polymerase-induced DNA bending.
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Unusual properties of promoter-up mutations in the Escherichia coli galactose operon and evidence suggesting RNA polymerase-induced DNA bending.

机译:大肠杆菌半乳糖操纵子中启动子向上突变的异常特性和表明RNA聚合酶诱导的DNA弯曲的证据。

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摘要

Two mutations are described, each of which renders the Pribnow box sequence of one of the two overlapping promoters of the Escherichia coli galactose operon identical to the consensus sequence TATAAT. Both double exchanges were specifically introduced into the original context by oligonucleotide-directed mutation construction. Each of the mutant promoters exhibits a greatly enhanced capacity to form stable complexes with RNA polymerase, as judged by nuclease protection experiments and by assaying shifts of electrophoretic mobility. On the other hand, the effect of the same mutations on the rates of transcription from the two gal promoters is strikingly different. Unexpectedly, when complexed with RNA polymerase, DNA fragments carrying one of the two double exchanges were found to differ from each other as well as from the corresponding wild-type fragment with respect to their electrophoretic mobilities. These observations are indicative of different three-dimensional structures of these complexes which may reflect different forms of DNA bending induced in these otherwise identical fragments by complex formation with RNA polymerase.
机译:描述了两个突变,每个突变使大肠杆菌半乳糖操纵子的两个重叠启动子之一的Pribnow盒序列与共有序列TATAAT相同。通过寡核苷酸定向的突变构建将两个双重交换特异性地引入原始背景。通过核酸酶保护实验和通过分析电泳迁移率的变化判断,每个突变启动子都具有大大增强的与RNA聚合酶形成稳定复合物的能力。另一方面,相同突变对两个gal启动子转录速率的影响却截然不同。出乎意料的是,当与RNA聚合酶复合时,发现带有两个双交换之一的DNA片段在电泳迁移率上彼此不同,并且与相应的野生型片段不同。这些观察结果表明这些复合物的三维结构不同,这可能反映了通过RNA聚合酶形成复合物在这些原本相同的片段中诱导的DNA弯曲的不同形式。

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