Rougvie A E, Lis J T
Section of Biochemistry, Cornell University, Ithaca, New York 14853.
Cell. 1988 Sep 9;54(6):795-804. doi: 10.1016/s0092-8674(88)91087-2.
Protein-DNA cross-linking of cultured Drosophila cells has shown that, in vivo, prior to the induction of heat shock, there is approximately one molecule of RNA polymerase II associated with the promoter region of the major heat shock gene, hsp70. Here, we show that this promoter-associated RNA polymerase II molecule is transcriptionally engaged and has formed a nascent RNA chain of approximately 25 nucleotides in length, but is apparently arrested at that point and unable to penetrate further into the hsp70 gene without heat induction. The detection of a post-initiation RNA polymerase complex on the promoter region of the inactive gene suggests that there is a transcriptional control mechanism that acts at a step early in transcript elongation.
对培养的果蝇细胞进行蛋白质 - DNA交联实验表明,在体内,热休克诱导之前,主要热休克基因hsp70的启动子区域大约结合有一个RNA聚合酶II分子。在此,我们发现,与启动子结合的这个RNA聚合酶II分子处于转录状态,并且已经形成了一条长度约为25个核苷酸的新生RNA链,但显然在这一点上停滞不前,未经热诱导就无法进一步转录hsp70基因。在无活性基因的启动子区域检测到起始后RNA聚合酶复合物,这表明存在一种转录控制机制,该机制作用于转录延伸的早期阶段。