A ratchet mechanism of transcription elongation and its control

被引:280
作者
Bar-Nahum, G
Epshtein, V
Ruckenstein, AE
Rafikov, R
Mustaev, A
Nudler, E [1 ]
机构
[1] NYU, Med Ctr, Dept Biochem, New York, NY 10016 USA
[2] Rutgers State Univ, BioMaPS Inst Quantitat Biol, Piscataway, NJ 08854 USA
[3] Rutgers State Univ, Dept Phys, Piscataway, NJ 08854 USA
[4] Publ Hlth Res Inst, Newark, NJ 07103 USA
关键词
D O I
10.1016/j.cell.2004.11.045
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
RNA chain elongation is a highly processive and accurate process that is finely regulated by numerous intrinsic and extrinsic signals. Here we describe a general mechanism that governs RNA polymerase (RNAP) movement and response to regulatory inputs such as pauses, terminators, and elongation factors. We show that E.coli RNAP moves by a complex Brownian ratchet mechanism, which acts prior to phosphodiester bond formation. The incoming substrate and the flexible F bridge domain of the catalytic center serve as two separate ratchet devices that function in concert to drive forward translocation. The adjacent G loop domain controls F bridge motion, thus keeping the proper balance between productive and inactive states of the elongation complex. This balance is critical for cell viability since it determines the rate, processivity, and fidelity of transcription.
引用
收藏
页码:183 / 193
页数:11
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