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降低大肠杆菌正调控操纵子malPQ表达的点突变。

Point mutations that reduce the expression of malPQ, a positively controlled operon of Escherichia coli.

作者信息

Gutierrez C, Raibaud O

出版信息

J Mol Biol. 1984 Jul 25;177(1):69-86. doi: 10.1016/0022-2836(84)90058-5.

Abstract

malPQ is one of three operons controlled by the positive regulator gene malT. With the objective of defining DNA sequences essential for malPQ transcription, we looked for cis-dominant mutations that reduced the level of expression of this operon. We first constructed malP-lac fusion strains, selected from one of them a series of mutants resistant to p-nitrophenyl-beta-D-thiogalactopyranoside (a bacteriostatic compound that enters the cells via lac permease), and retained the clones that contained a mutation reducing the expression of the hybrid operon in a cis-dominant fashion. Nineteen such mutations were sequenced, and their effect on an otherwise wild type malPQ operon was studied. Three of them mapped in a transcribed portion of the operon, and are believed to exert their effect at the translation level. The others map upstream from the transcription startpoint (co-ordinate +1) and help define three DNA segments that must play a predominant role in transcription initiation: the Pribnow box (from positions -7 to -12); and two inverted repeats, extending from position -32 to -36, and -59 to -63, respectively, which are proposed to constitute part of the binding site for MalT protein.

摘要

malPQ是受正调控基因malT控制的三个操纵子之一。为了确定malPQ转录所必需的DNA序列,我们寻找了能降低该操纵子表达水平的顺式显性突变。我们首先构建了malP-lac融合菌株,从其中选出一系列对对硝基苯基-β-D-硫代半乳糖苷(一种通过乳糖通透酶进入细胞的抑菌化合物)有抗性的突变体,并保留了那些含有以顺式显性方式降低杂合操纵子表达的突变的克隆。对其中十九个这样的突变进行了测序,并研究了它们对野生型malPQ操纵子的影响。其中三个位于操纵子的转录部分,据信它们在翻译水平发挥作用。其他的位于转录起始点(坐标+1)上游,有助于确定在转录起始中必须起主要作用的三个DNA片段:Pribnow框(从-7到-12位);以及两个反向重复序列,分别从-32到-36位和-59到-63位延伸,它们被认为构成MalT蛋白结合位点的一部分。

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