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枯草芽孢杆菌DNA损伤诱导型启动子区域的克隆与特性分析

Cloning and characterization of DNA damage-inducible promoter regions from Bacillus subtilis.

作者信息

Cheo D L, Bayles K W, Yasbin R E

机构信息

Department of Biological Sciences, University of Maryland, Baltimore 21228.

出版信息

J Bacteriol. 1991 Mar;173(5):1696-703. doi: 10.1128/jb.173.5.1696-1703.1991.

Abstract

DNA damage-inducible (din) genes in Bacillus subtilis are coordinately regulated and together compose a global regulatory network that has been termed the SOS-like or SOB regulon. To elucidate the mechanisms of SOB regulation, operator/promoter regions from three din loci (dinA, dinB, and dinC) of B. subtilis were cloned. Operon fusions constructed with these cloned din promoter regions rendered reporter genes damage inducible in B. subtilis. Induction of all three din promoters was dependent upon a functional RecA protein. Analysis of these fusions has localized sequences required for damage-inducible expression of the dinA, dinB, and dinC promoters to within 120-, 462-, and 139-bp regions, respectively. Comparison of the nucleotide sequences of these three din promoters with the recA promoter, as well as with the promoters of other loci associated with DNA repair in B. subtilis, has identified the consensus sequence GAAC-N4-GTTC as a putative SOB operator site.

摘要

枯草芽孢杆菌中的DNA损伤诱导(din)基因受到协同调控,共同构成了一个被称为SOS样或SOB调节子的全局调控网络。为了阐明SOB调控的机制,克隆了枯草芽孢杆菌三个din位点(dinA、dinB和dinC)的操纵子/启动子区域。用这些克隆的din启动子区域构建的操纵子融合使报告基因在枯草芽孢杆菌中可被损伤诱导。所有三个din启动子的诱导都依赖于功能性的RecA蛋白。对这些融合体的分析已将dinA、dinB和dinC启动子损伤诱导表达所需的序列分别定位在120bp、462bp和139bp区域内。将这三个din启动子的核苷酸序列与recA启动子以及与枯草芽孢杆菌中与DNA修复相关的其他位点的启动子进行比较,已确定共有序列GAAC-N4-GTTC为假定的SOB操纵位点。

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