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大肠杆菌中lysU上游Lrp结合区域的结构-功能关系

Structure-function relationship of the Lrp-binding region upstream of lysU in Escherichia coli.

作者信息

Gazeau M, Delort F, Fromant M, Dessen P, Blanquet S, Plateau P

机构信息

Laboratoire de Biochimie, URA 240 CNRS, Ecole Polytechnique, Palaiseau, France.

出版信息

J Mol Biol. 1994 Aug 19;241(3):378-89. doi: 10.1006/jmbi.1994.1514.

Abstract

In Escherichia coli, one of the two genes encoding lysyl-tRNA synthetase, lysU, belongs to the regulon controlled by the leucine-responsive regulatory protein (Lrp). To map the site of Lrp action, mutants escaping regulation in rich medium were generated through random mutagenesis of the lysU promoter region. The mutations showed parallel effects on the strength of Lrp-DNA association, as measured in vitro by gel retardation experiments, and on the degree of repression of lysU expression by Lrp in vivo. In addition, DNase I and hydroxyl radical footprinting experiments indicated that several Lrp molecules bind to a DNA region of over 110 bp in a highly cooperative manner. This region, which encompasses the -35 box of the lysU promoter, was the target of all the mutations affecting the strength of the Lrp-DNA association. These mutations are frequently located in short A + T-rich runs distributed along the Lrp binding region with a periodicity of one helix turn. Because we could find such a regular alternance of A + T runs upstream of several other Lrp-regulated genes, we suggest that this pattern is one feature indicative of the binding of Lrp.

摘要

在大肠杆菌中,编码赖氨酰 - tRNA合成酶的两个基因之一lysU,属于由亮氨酸应答调节蛋白(Lrp)控制的调节子。为了定位Lrp作用位点,通过对lysU启动子区域进行随机诱变,在丰富培养基中产生了逃避调节的突变体。这些突变在体外通过凝胶阻滞实验测定的Lrp - DNA结合强度以及体内Lrp对lysU表达的抑制程度上表现出平行效应。此外,DNase I和羟自由基足迹实验表明,几个Lrp分子以高度协同的方式结合到超过110 bp的DNA区域。该区域包含lysU启动子的 - 35框,是所有影响Lrp - DNA结合强度的突变的靶点。这些突变经常位于沿着Lrp结合区域分布的富含A + T的短序列中,其周期为一个螺旋圈。因为我们在其他几个Lrp调节基因的上游也能发现这种A + T序列的规则交替,所以我们认为这种模式是Lrp结合的一个指示特征。

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