Tsao Y P, Wu H Y, Liu L F
Department of Biological Chemistry, Johns Hopkins School of Medicine, Baltimore, Maryland 21205.
Cell. 1989 Jan 13;56(1):111-8. doi: 10.1016/0092-8674(89)90989-6.
The translocation of an RNA polymerase elongation complex along double helical DNA has been proposed to generate positive supercoiling waves ahead of and negative supercoiling waves behind the transcription ensemble. This twin supercoiled domain model has been tested in vitro. In the presence of prokaryotic DNA topoisomerase I, which selectively removes negative supercoils, transcription from a single promoter results in rapid and extensive positive supercoiling of the DNA template. The accumulation of positive supercoils in the DNA template requires continued movement of the elongation complex as well as sizable nascent RNA chains. These in vitro results provide direct biochemical evidence supporting the twin supercoiled domain model of transcription. Furthermore, the magnitute of DNA supercoiling (torsional) waves generated by transcription is much greater than previously expected, suggesting that transcription is one of the principal factors affecting intracellular DNA supercoiling.
有人提出,RNA聚合酶延伸复合物沿双螺旋DNA的移位会在转录整体之前产生正超螺旋波,并在其后产生负超螺旋波。这种双超螺旋结构域模型已在体外进行了测试。在原核DNA拓扑异构酶I存在的情况下,该酶可选择性地去除负超螺旋,从单个启动子进行转录会导致DNA模板迅速而广泛地形成正超螺旋。DNA模板中正超螺旋的积累需要延伸复合物的持续移动以及相当长的新生RNA链。这些体外实验结果提供了直接的生化证据,支持转录的双超螺旋结构域模型。此外,转录产生的DNA超螺旋(扭转)波的幅度比之前预期的要大得多,这表明转录是影响细胞内DNA超螺旋的主要因素之一。