Le Grice S F, Matzura H, Marcoli R, Iida S, Bickle T A
J Bacteriol. 1982 Apr;150(1):312-8. doi: 10.1128/jb.150.1.312-318.1982.
DNase I protection experiments have indicated that the cyclic AMP-catabolite gene activator protein complex binds to two regions preceding the chloramphenicol acetyl transferase (cat) gene in Escherichia coli. One of these lies adjacent to the RNA polymerase binding site, whereas the second lies approximately 130 base pairs upstream from the starting point of transcription. Additional DNase protection experiments and in vitro transcription experiments with modified templates indicate that the catabolite gene activator protein site proximal to the cat promoter functions independently of the distal site, indicating that in vitro the second of these sites is not required for transcriptional activation of the cat gene.
脱氧核糖核酸酶I保护实验表明,环磷酸腺苷 - 分解代谢物基因激活蛋白复合物与大肠杆菌中氯霉素乙酰转移酶(cat)基因之前的两个区域结合。其中一个区域毗邻RNA聚合酶结合位点,而另一个区域位于转录起始点上游约130个碱基对处。额外的脱氧核糖核酸酶保护实验以及使用修饰模板进行的体外转录实验表明,靠近cat启动子的分解代谢物基因激活蛋白位点独立于远端位点发挥作用,这表明在体外,cat基因转录激活不需要这些位点中的第二个位点。