Sequence-dependent kinetic model for transcription elongation by RNA polymerase

被引:121
|
作者
Bai, L [1 ]
Shundrovsky, A [1 ]
Wang, MD [1 ]
机构
[1] Cornell Univ, Atom & Solid State Phys Lab, Dept Phys, Ithaca, NY 14853 USA
基金
美国国家卫生研究院;
关键词
RNA polymerase; transcription; kinetics; sequence-dependence; model;
D O I
10.1016/j.jmb.2004.08.107
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We present a kinetic model for the sequence-dependent motion of RNA polymerase (RNAP) during transcription elongation. For each NTP incorporation, RNAP has a net forward translocation of one base-pair along the DNA template. However, this process may involve the exploration of back-tracked and forward-tracked translocation modes. In our model, the kinetic rates for the reaction pathway, calculated based on the stabilities of the transcription elongation complex (TEC), necessarily lead to sequence-dependent NTP incorporation rates. Simulated RNAP elongation kinetics is in good agreement with data from transcription gels and single-molecule studies. The model provides a kinetic explanation for well-known back-tracked pauses at transcript positions with unstable TECs. It also predicts a new type of pause caused by an energetically unfavorable transition from pre to post-translocation modes. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:335 / 349
页数:15
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