DNA binding and DNA bending by the MelR transcription activator protein from Escherichia coli

被引:31
作者
Bourgerie, SJ
Michan, CM
Thomas, MS
Busby, SJW
Hyde, EI
机构
[1] UNIV BIRMINGHAM, SCH BIOCHEM, BIRMINGHAM B15 2TT, W MIDLANDS, ENGLAND
[2] UNIV SHEFFIELD, SCH MED, DEPT MED MICROBIOL, SHEFFIELD, S YORKSHIRE, ENGLAND
基金
英国生物技术与生命科学研究理事会;
关键词
D O I
10.1093/nar/25.9.1685
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 melR gene encodes MelR protein which is a member of the AraC/XylS family of bacterial transcription activators, The function of MelR was investigated by making a targeted deletion in the melR gene of the Escherichia coli chromosome, MelR is a transcription activator essential for melibiose-dependent expression of the melAB operon which is needed for bacterial growth with melibiose as a carbon source. To investigate the interactions of MelR at the melAB promoter, both full length MelR and a shortened derivative, MelR173, containing the C-terminal DNA-binding domain, were purified as fusions to glutathione-S-transferase. Circular permutation studies show that both full-length MelR and MelR173 induce an apparent bend upon binding to target sites at the melAB promoter, Bound full-length MelR, but not MelR173, can oligomerise to form larger complexes that are likely to be involved in transcription activation.
引用
收藏
页码:1685 / 1693
页数:9
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