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对由CRP和CytR形成的用于抑制作用的启动子识别复合物,以及由CRP和RNA聚合酶形成的用于激活大肠杆菌deoP2启动子转录的启动子识别复合物的表征。

Characterization of promoter recognition complexes formed by CRP and CytR for repression and by CRP and RNA polymerase for activation of transcription on the Escherichia coli deoP2 promoter.

作者信息

Møllegaard N E, Rasmussen P B, Valentin-Hansen P, Nielsen P E

机构信息

Department of Biochemistry B, Panum Institute, University of Copenhagen, Denmark.

出版信息

J Biol Chem. 1993 Aug 15;268(23):17471-7.

PMID:8394345
Abstract

The structure of the cAMP-CRP-CytR repression complex and the cAMP CRP-RNA polymerase initiation complex at the deoP2 promoter of E. coli have been probed by DNase I and uranyl footprinting. In the CRP2-CytR complex all protein DNA-phosphate contacts at CRP-1 and CRP-2 are retained, and in addition two new minor groove contacts, ascribed to phosphate-CytR interactions, are observed at -60 between the CRP sites. The contacts are compatible with a model in which the promoter DNA is wrapped around a complex of two CRPs and one CytR. In the RNA polymerase-CRP complex, the CRP-1 phosphate contacts are almost identical to those seen in the repression complex and strong RNA polymerase contacts are seen in the -10 and in the +10 regions. Most noteworthy are minor groove contacts in the -60 region ascribed to RNA polymerase contacts upstream from the CRP. Furthermore, binding of CRP to the CRP-2 target does not seem to interfere with RNA polymerase binding. Thus, a model is suggested in which the DNA is wrapped around a complex of RNA polymerase and one CRP. Finally, the results show that CytR and RNA polymerase are rivals that compete for binding with CRP at deoP2 and that CytR functions as an antiactivator.

摘要

利用DNase I和铀酰足迹法探究了大肠杆菌deoP2启动子处的cAMP-CRP-CytR阻遏复合物以及cAMP CRP-RNA聚合酶起始复合物的结构。在CRP2-CytR复合物中,CRP-1和CRP-2处所有蛋白质与DNA磷酸基团的接触得以保留,此外,在CRP位点之间的-60处观察到两个新的归因于磷酸基团与CytR相互作用的小沟接触。这些接触与一种模型相符,即启动子DNA缠绕在两个CRP和一个CytR的复合物周围。在RNA聚合酶-CRP复合物中,CRP-1磷酸基团的接触与阻遏复合物中的几乎相同,并且在-10和+10区域观察到了强烈的RNA聚合酶接触。最值得注意的是在-60区域的小沟接触,归因于CRP上游的RNA聚合酶接触。此外,CRP与CRP-2靶点的结合似乎并不干扰RNA聚合酶的结合。因此,提出了一种模型,即DNA缠绕在RNA聚合酶和一个CRP的复合物周围。最后,结果表明CytR和RNA聚合酶是竞争对手,它们在deoP2处竞争与CRP的结合,并且CytR起到抗激活剂的作用。

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