DNA flexibility of the UP element is a major determinant for transcriptional activation at the Escherichia coli acetate promoter

被引:16
作者
Negre, D
BonodBidaud, C
Oudot, C
Prost, JF
Kolb, A
Ishihama, A
Cozzone, AJ
Cortay, JC
机构
[1] INST BIOL & CHIM PROT,CNRS,F-69367 LYON,FRANCE
[2] INST PASTEUR,F-75724 PARIS,FRANCE
[3] NATL INST GENET,DEPT MOL GENET,MISHIMA,SHIZUOKA 411,JAPAN
关键词
D O I
10.1093/nar/25.4.713
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 specific interaction of the upstream element-containing promoter of the Escherichia coli acetate operon with either the RNA polymerase holoenzyme or its alpha subunit has been analyzed by the base removal method, Our results indicate that: (i) direct and specific base contacts can be detected in the acetate promoter-alpha subunit complex; (ii) base elimination in the upstream element of the acetate promoter enhances the binding of RNA polymerase. A similar effect is observed when studying the interactions between RNA polymerase and the rrnB ribosomal operon P1 promoter.
引用
收藏
页码:713 / 718
页数:6
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