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鉴定对OmpR-DNA相互作用至关重要的碱基对。

Identification of base pairs important for OmpR-DNA interaction.

作者信息

Pratt L A, Silhavy T J

机构信息

Department of Molecular Biology, Princeton University, New Jersey 08544, USA.

出版信息

Mol Microbiol. 1995 Aug;17(3):565-73. doi: 10.1111/j.1365-2958.1995.mmi_17030565.x.

Abstract

OmpR, the transcriptional regulator of the ompF and ompC porin genes, is a member of a novel class of DNA-binding proteins. The mechanism(s) by which this class of proteins interacts with target DNA sites is not understood. To address this issue, we investigated the nature of the DNA sequences recognized by OmpR. A 36 bp DNA fragment was identified that is capable of supporting OmpR-DNA interaction in vivo. The base pairs within this region of DNA that are critical to this interaction were identified by isolating mutations within the fragment that hinder normal OmpR-DNA binding. The results obtained provide insights concerning the nature of the sequences recognized by OmpR and also support a model in which co-operative binding is involved in OmpR-DNA interaction.

摘要

OmpR是外膜孔蛋白基因ompF和ompC的转录调节因子,是一类新型DNA结合蛋白的成员。这类蛋白质与靶DNA位点相互作用的机制尚不清楚。为了解决这个问题,我们研究了OmpR识别的DNA序列的性质。鉴定出一个36bp的DNA片段,它能够在体内支持OmpR与DNA的相互作用。通过分离该片段内阻碍正常OmpR与DNA结合的突变,确定了该DNA区域内对这种相互作用至关重要的碱基对。所得结果提供了有关OmpR识别序列性质的见解,也支持了一种模型,即协同结合参与了OmpR与DNA的相互作用。

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