Role of open complex instability in kinetic promoter selection by bacteriophage T7 RNA polymerase

被引:49
作者
Villemain, J [1 ]
Guajardo, R [1 ]
Sousa, R [1 ]
机构
[1] UNIV TEXAS,HLTH SCI CTR,DEPT BIOCHEM,SAN ANTONIO,TX 78212
关键词
T7 RNA polymerase; transcription initiation; open complex; promoters;
D O I
10.1006/jmbi.1997.1358
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
By measuring steady-state rates of dinucleotide synthesis on double-stranded (d.s.) and partially single-stranded (p.s.s.) promoters, and topological unwinding due to open complex formation on plasmids, we have obtained evidence that open complex formation in bacteriophage T7 RNA polymerase:promoter binary complexes is thermodynamically disfavored and that the rate of collapse of the open complex is competitive with the rate of transcription initiation. It is suggested that open complex instability is a kinetic mechanism that allows T7 RNA polymerase (RNAP) to achieve promoter specificity while still allowing for efficient promoter release. Open complex instability could also provide a mechanism for modulating the K-M for the initiating NTPs so as to allow different promoters to respond differently to physiological changes in NTP concentration. (C) 1997 Academic Press Limited.
引用
收藏
页码:958 / 977
页数:20
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