Mechanism of transcriptional activation by FIS: Role of core promoter structure and DNA topology

被引:47
作者
Auner, H
Buckle, M
Deufel, A
Kutateladze, T
Lazarus, L
Mavathur, R
Muskhelishvili, G
Pemberton, I
Schneider, R
Travers, A
机构
[1] LMU, Inst Genet & Mikrobiol, D-80638 Munich, Germany
[2] Ecole Normale Super, LBPA, CNRS, UMR 8113, F-94235 Cachan, France
[3] Georgian Acad Sci, Inst Mol Biol & Biol Phys, GE-380060 Tbilisi, Georgia
[4] MRC, Mol Biol Lab, Cambridge CB2 2QH, England
[5] Max Planck Inst Terr Mikrobiol, D-35043 Marburg, Germany
关键词
promoter structure; DNA supercoiling; FIS; transcription activation;
D O I
10.1016/S0022-2836(03)00727-7
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
The Escherichia coli DNA architectural protein FIS activates transcription from stable RNA promoters on entry into exponential growth and also reduces the level of negative supercoiling. Here we show that such a reduction decreases the activity of the tyrT promoter but that activation by FIS rescues tyrT transcription at non-optimal superhelical densities. Additionally we show that three different "up" mutations in the tyrT core promoter either abolish or reduce the dependence of tyrT transcription on both high negative superhelicity and FIS in vivo and infer that the specific sequence organisation of the core promoter couples the control of transcription initiation by negative superhelicity and FIS. In vitro all the mutations potentiate FIS-independent untwisting of the - 10 region while at the wild-type promoter FIS facilitates this step. We propose that this untwisting is a crucial limiting step in the initiation of tyrT RNA synthesis. The tyrT core promoter structure is thus optimised to combine high transcriptional activity with acute sensitivity to at least three major independent regulatory inputs: negative superhelicity, FIS and ppGpp. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:331 / 344
页数:14
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