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一种具有改变的启动子特异性的RNA聚合酶的突变型大肠杆菌σ70亚基。

A mutant Escherichia coli sigma 70 subunit of RNA polymerase with altered promoter specificity.

作者信息

Gardella T, Moyle H, Susskind M M

机构信息

Department of Molecular Genetics and Microbiology, University of Massachusetts Medical School, Worcester 01605.

出版信息

J Mol Biol. 1989 Apr 20;206(4):579-90. doi: 10.1016/0022-2836(89)90567-6.

Abstract

A mutation is described that alters the promoter specificity of sigma 70, the primary sigma factor of Escherichia coli RNA polymerase. In strains carrying both the mutant and wild-type sigma gene (rpoD), the mutant sigma causes a large increase in the activity of mutant P22 ant promoters with A.T or C.G instead of the wild-type, consensus G.C base-pair at position -33, the third position of the consensus -35 hexamer 5'-TTGACA-3'. There is little or no effect on the activities of the wild-type and 23 other mutant ant promoters, including one with T.A at -33. The mutant sigma also activates E. coli lac promoters with A.T or C.G, but not T.A, at the corresponding position. The rpoD mutation (rpoD-RH588) changes a CGT codon to CAT. The corresponding change in sigma 70 is Arg588----His. This residue is in a region that is conserved among most sigma factors, a region that is also homologous with the helix-turn-helix motif of DNA-binding proteins. These results suggest that this region of sigma 70 is directly involved in recognition of the -35 hexamer.

摘要

本文描述了一种突变,该突变改变了大肠杆菌RNA聚合酶的主要σ因子σ70的启动子特异性。在同时携带突变型和野生型σ基因(rpoD)的菌株中,突变型σ会导致突变型P22 ant启动子的活性大幅增加,这些启动子在-33位(即共有序列-35六聚体5'-TTGACA-3'的第三个位置)具有A.T或C.G碱基对,而非野生型的共有G.C碱基对。对野生型和其他23种突变型ant启动子的活性几乎没有影响,包括在-33位具有T.A的启动子。突变型σ还能激活在相应位置具有A.T或C.G而非T.A的大肠杆菌lac启动子。rpoD突变(rpoD-RH588)将CGT密码子变为CAT。σ70中相应的变化是Arg588变为His。该残基位于大多数σ因子中保守的区域,该区域也与DNA结合蛋白的螺旋-转角-螺旋基序同源。这些结果表明,σ70的该区域直接参与对-35六聚体的识别。

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