Schmitz M L, Maier U G, Brown J W, Feix G
Institut für Biologie III, Albert-Ludwigs-Universität, Freiburg, Federal Republic of Germany.
J Biol Chem. 1989 Jan 25;264(3):1467-72.
The external spacer region of a nuclear rRNA gene unit of maize was analyzed for binding of nuclear proteins and revealed binding to the promoter region and to the 200-base pair repeat elements upstream of the promoter. The promoter binding site was further characterized by DNase I and exonuclease III foot-printing as well as by gel shift and South-Western experiments, revealing the binding of several proteins. Competition experiments indicate that the protein which interacts with the repeat units also binds to the promoter region. A model for the combined action of both binding regions in the regulation of transcription is presented.
对玉米核rRNA基因单位的外部间隔区进行了核蛋白结合分析,结果显示其与启动子区域以及启动子上游200个碱基对的重复元件存在结合。通过DNA酶I和核酸外切酶III足迹分析以及凝胶迁移和蛋白质印迹实验,对启动子结合位点进行了进一步表征,揭示了几种蛋白质的结合情况。竞争实验表明,与重复单位相互作用的蛋白质也与启动子区域结合。本文提出了一个关于这两个结合区域在转录调控中联合作用的模型。