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

机译:鉴定参与调节链霉菌的Sureofaciens Sigf基因的调节的DNA结合蛋白,其编码孢子σf因子σf

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Expression of the sigF gene encoding a sporulation-specific sigma factor, σF, 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.
机译:编码孢子化特异性Sigma因子σf的SigF基因的表达仅限于孢子菌。使用来自S. aureofaciens的不同发​​育阶段的蛋白质级分的凝胶迁移率测定显示出两种不同的推定蛋白,特异性地与Sigf启动子区中出现:存在于幼粒菌丝体中的蛋白质(指定的RSFA)和存在的蛋白质(指定的RSFB)孢子课程。基于在分化期间外观的特征谱,RSFA可能是抑制器和RSFB的SIGF表达式。通过启动子缺失片段的凝胶迁移率转移测定和通过DNA酶I脚印分析测定抑制蛋白(RSFA)的特异性结合位点的位置。相对于SIGF启动子的转录起点,并重叠α87至25的结合位点,并重叠α35启动子区域。鉴于Sigf表达对HIH的依赖性,推定的孢子化转录因子HHIH在大肠杆菌中过度引发,并在用SIGF启动子进行迁移率转换测定。然而,没有检测到特异性结合,表明SIGF在WHIH上的间接依赖性。

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