Dandanell G, Valentin-Hansen P, Larsen J E, Hammer K
Nature. 1987;325(6107):823-6. doi: 10.1038/325823a0.
Regulation of transcription initiation by proteins binding at DNA sequences some distance from the promoter region itself seems to be a general phenomenon in both eukaryotes and prokaryotes. Proteins bound to an enhancer site in eukaryotes can turn on a distant gene, whereas efficient repression of some prokaryotic genes such as the gal, ara and deo operons of Escherichia coli, requires the presence of two operator sites, separated by 110, 200 and 600 base pairs (bp) respectively. In the deo operon, which encodes nucleoside catabolizing enzymes, we have shown that efficient and cooperative repression can be obtained when the distance between the two sites ranges from 224 to 997 bp. Here, we report that transcription initiation can be regulated from an operator site placed 1 to 5 kilobases (kb) downstream of the deoP2 promoter (and downstream of the transcribed gene), and present the first experimental data for prokaryotic regulation at distances greater than 1 kb. Our results support the model of DNA loop formation as a common regulatory mechanism explaining both some prokaryotic regulation and the action of eukaryotic enhancers.
蛋白质结合在距离启动子区域本身有一定距离的DNA序列上对转录起始进行调控,这似乎是真核生物和原核生物中的普遍现象。真核生物中与增强子位点结合的蛋白质能够开启一个远距离的基因,而对于一些原核基因,如大肠杆菌的gal、ara和deo操纵子,有效的阻遏需要存在两个操纵位点,它们分别被110、200和600个碱基对(bp)隔开。在编码核苷分解代谢酶的deo操纵子中,我们已经表明,当两个位点之间的距离在224到997 bp之间时,可以实现高效的协同阻遏。在此,我们报告转录起始可以从位于deoP2启动子下游1至5千碱基(kb)(以及转录基因下游)的一个操纵位点进行调控,并给出了原核生物在大于1 kb距离处调控的首个实验数据。我们的结果支持DNA环形成模型,该模型作为一种常见的调控机制,解释了一些原核生物的调控以及真核生物增强子的作用。