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鉴定参与调控金色链霉菌sigF基因表达的DNA结合蛋白,该基因编码孢子形成σ因子σ(F)。

Identification of DNA-binding proteins involved in regulation of expression of the Streptomyces aureofaciens sigF gene, which encodes sporulation sigma factor sigma(F).

作者信息

Homerová D, Ševčı Ková B, Sprušanský O, Kormanec J

机构信息

Institute of Molecular Biology, Slovak Academy of Sciences, Dubravská cesta 21, 842 51 Bratislava, Slovak Republic1.

出版信息

Microbiology (Reading). 2000 Nov;146 ( Pt 11):2919-2928. doi: 10.1099/00221287-146-11-2919.

Abstract

Expression of the sigF gene encoding a sporulation-specific sigma factor, sigma(F), in Streptomyces aureofaciens is restricted only to sporulation. Gel mobility-shift assays using protein fractions from different developmental stages of S. aureofaciens revealed two different putative proteins specifically bound to the sigF promoter region: a protein (designated RsfA) present in young substrate mycelium, and a protein (designated RsfB) present in the course of sporulation. Based on the characteristic profiles of their appearance during differentiation, RsfA might be a repressor and RsfB an activator of sigF expression. The location of a specific binding site of the repressor-like protein (RsfA) was determined by gel mobility-shift assays of promoter deletion fragments and by DNase I footprinting analysis. The binding site mapped from nucleotides -87 to -25 relative to the transcription start point of the sigF promoter, and overlapped the -35 promoter region. Given the dependence of sigF expression upon whiH, the putative sporulation transcription factor WhiH was overproduced in Escherichia coli and used in the mobility-shift assays with the sigF promoter. However, no specific binding was detected, indicating an indirect dependence of sigF upon whiH.

摘要

编码芽孢形成特异性σ因子σ(F)的sigF基因在金色链霉菌中的表达仅局限于芽孢形成阶段。利用金色链霉菌不同发育阶段的蛋白质组分进行凝胶迁移率变动分析,结果显示有两种不同的假定蛋白能特异性结合到sigF启动子区域:一种蛋白(命名为RsfA)存在于幼龄基质菌丝体中,另一种蛋白(命名为RsfB)存在于芽孢形成过程中。根据它们在分化过程中出现的特征图谱,RsfA可能是sigF表达的阻遏物,而RsfB是激活物。通过对启动子缺失片段进行凝胶迁移率变动分析以及DNase I足迹分析,确定了类阻遏蛋白(RsfA)特异性结合位点的位置。该结合位点位于相对于sigF启动子转录起始点的核苷酸-87至-25处,与-35启动子区域重叠。鉴于sigF表达对whiH的依赖性,假定的芽孢形成转录因子WhiH在大肠杆菌中过量表达,并用于与sigF启动子的迁移率变动分析。然而,未检测到特异性结合,这表明sigF对whiH存在间接依赖性。

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