Greene E A, Spiegelman G B
Department of Microbiology and Immunology, University of British Columbia, Vancouver, Canada.
J Biol Chem. 1996 May 10;271(19):11455-61. doi: 10.1074/jbc.271.19.11455.
Repression of transcription of the abrB gene is essential to expression of many of the postexponential genes in Bacillus. The repression is due to the activity of the response regulator protein Spo0A. We have used in vitro transcription and DNase I and hydroxyl radical footprinting to explore the mechanism of transcription inhibition. Spo0A binds to specific DNA sequences (0A boxes), and two such boxes are found downstream of the tandem promoters for the abrB gene. The data indicate that both RNA polymerase and Spo0A bind simultaneously to a DNA fragment containing the promoters and the 0A boxes. The Spo0A prevents the polymerase from inducing DNA strand denaturation at the promoter for the abrB gene.
对芽孢杆菌中许多指数后期基因的表达而言,abrB基因转录的抑制作用至关重要。这种抑制作用归因于应答调节蛋白Spo0A的活性。我们利用体外转录以及DNase I和羟自由基足迹法来探究转录抑制的机制。Spo0A与特定的DNA序列(0A框)结合,并且在abrB基因的串联启动子下游发现了两个这样的框。数据表明RNA聚合酶和Spo0A同时与包含启动子和0A框的DNA片段结合。Spo0A阻止聚合酶在abrB基因的启动子处诱导DNA链变性。