Wang D, Meier T I, Chan C L, Feng G, Lee D N, Landick R
Department of Biology, Washington University, St. Louis, Missouri 63130, USA.
Cell. 1995 May 5;81(3):341-50. doi: 10.1016/0092-8674(95)90387-9.
A central enigma of transcriptional regulation is how the normally efficient transcription elongation complex stops at pause and termination signals. One possibility, raised by the discovery that RNA polymerase sometimes contracts its DNA footprint, is that discontinuous movements contribute to recognizing these signals. We report that E. coli RNA polymerase responds to sequences immediately downstream and upstream from the his leader pause site by changing neither its downstream DNA contact nor its upstream RNA contact for 8 bp preceding the pause. This compressed complex isomerizes to a paused conformation by an approximately 10 bp jump of its downstream DNA contact and simultaneous extrusion of an RNA hairpin that stabilizes the paused conformation. We suggest pausing and termination could be alternative outcomes of a similar isomerization that depend on the strength of contacts to 3'-proximal RNA remaining after the jump.
转录调控的一个核心谜团是,正常高效的转录延伸复合物如何在暂停和终止信号处停止。RNA聚合酶有时会收缩其DNA足迹这一发现提出了一种可能性,即不连续运动有助于识别这些信号。我们报告称,大肠杆菌RNA聚合酶对his前导序列暂停位点下游和上游的序列做出反应,在暂停前的8个碱基对中,其下游DNA接触和上游RNA接触均未发生变化。这种压缩复合物通过其下游DNA接触大约10个碱基对的跳跃以及同时挤出一个稳定暂停构象的RNA发夹,异构化为暂停构象。我们认为,暂停和终止可能是类似异构化的不同结果,这取决于跳跃后与3'近端RNA接触的强度。