Nudler E, Goldfarb A, Kashlev M
Public Health Research Institute, New York, NY 10016.
Science. 1994 Aug 5;265(5173):793-6. doi: 10.1126/science.8047884.
During transcription elongation, three flexibly connected parts of RNA polymerase of Escherichia coli advance along the template so that the front-end domain is followed by the catalytic site which in turn is followed by the RNA product binding site. The advancing enzyme was found to maintain the same conformation throughout extended segments of the transcribed region. However, when the polymerase traveled across certain DNA sites that seemed to briefly anchor the front-end domain, cyclic shifting of the three parts, accompanied by buildup and relief of internal strain, was observed. Thus, elongation proceeded in alternating laps of monotonous and inchworm-like movement with the flexible RNA polymerase configuration being subject to direct sequence control.
在转录延伸过程中,大肠杆菌RNA聚合酶的三个柔性连接部分沿着模板前进,使得前端结构域之后是催化位点,催化位点之后又是RNA产物结合位点。研究发现,前进的酶在转录区域的延伸片段中保持相同的构象。然而,当聚合酶穿过某些似乎能短暂固定前端结构域的DNA位点时,观察到这三个部分的循环移位,同时伴随着内部应变的积累和缓解。因此,延伸过程以单调运动和类似尺蠖运动的交替阶段进行,柔性的RNA聚合酶构型受到直接的序列控制。