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大肠杆菌ilvYC操纵子 divergent转录启动子之间的DNA超螺旋依赖性转录偶联与启动子强度和转录本长度成正比。

DNA supercoiling-dependent transcriptional coupling between the divergently transcribed promoters of the ilvYC operon of Escherichia coli is proportional to promoter strengths and transcript lengths.

作者信息

Opel M L, Hatfield G W

机构信息

Department of Microbiology and Molecular Genetics, College of Medicine, University of California, Irvine, CA 92697, USA.

出版信息

Mol Microbiol. 2001 Jan;39(1):191-8. doi: 10.1046/j.1365-2958.2001.02249.x.

Abstract

The twin-domain model of Liu and Wang suggested that high levels of DNA supercoiling generated in the region between closely spaced divergently transcribed promoters could serve to couple the activities of these promoters transcriptionally. In this report, we use topoisomer sets of defined superhelical densities as DNA templates in a purified in vitro transcription system to demonstrate transcriptional coupling between the divergently transcribed ilvY and ilvC promoters of the ilvYC operon of Escherichia coli. Current evidence for this type of DNA supercoiling-dependent transcriptional coupling, based largely on the in vivo activities of promoters contained in engineered DNA constructs, suggests that the transcription complex must be physically hindered to generate DNA supercoils and to prevent their diffusion throughout the DNA duplex. However, the in vitro results presented here demonstrate that (i) transcriptional coupling is observed between the divergent promoters of the ilvYC operon in the absence of transcript anchoring; (ii) the magnitude of the negative DNA supercoiling generated in the divergent promoter region is proportional to the sum of the global and transcription-induced superhelicity; and (iii) the magnitude of this transcription-induced superhelicity is proportional to promoter strengths and transcript lengths.

摘要

刘和王的双结构域模型表明,在紧密间隔的反向转录启动子之间的区域产生的高水平DNA超螺旋可在转录上耦合这些启动子的活性。在本报告中,我们在纯化的体外转录系统中使用具有确定超螺旋密度的拓扑异构酶集作为DNA模板,以证明大肠杆菌ilvYC操纵子的反向转录的ilvY和ilvC启动子之间的转录偶联。目前关于这种类型的DNA超螺旋依赖性转录偶联的证据,很大程度上基于工程化DNA构建体中所含启动子的体内活性,表明转录复合物必须受到物理阻碍才能产生DNA超螺旋并防止其在整个DNA双链体中扩散。然而,此处给出的体外结果表明:(i)在没有转录本锚定的情况下,在ilvYC操纵子的反向启动子之间观察到转录偶联;(ii)在反向启动子区域产生的负DNA超螺旋的大小与全局和转录诱导的超螺旋度之和成正比;(iii)这种转录诱导的超螺旋度的大小与启动子强度和转录本长度成正比。

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