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大肠杆菌RNA聚合酶在超螺旋模板上起始转录的机制。

Mechanism of initiation of transcription by Escherichia coli RNA polymerase on supercoiled template.

作者信息

Mishra R K, Chatterji D

机构信息

Centre for Cellular and Molecular Biology, Hyderabad, India.

出版信息

Mol Microbiol. 1993 May;8(3):507-15. doi: 10.1111/j.1365-2958.1993.tb01594.x.

Abstract

DNA supercoiling is known to influence the pattern of gene expression in prokaryotes. Thus the mechanism of transcription initiation and the topological state of the template are intimately related. Using in vitro reconstituted transcription assays, composed of purified RNA polymerase and promoters in their natural topological state, we have conducted a detailed study of transcription initiation from T7 early promoters including the following steps: the formation of ternary complexes, acquisition of rifampicin resistance, release of sigma factor and the capacity for RNA chain elongation in complexes. We determined the order of these events and the length of the transcripts when each step occurred during initiation of transcription on supercoiled templates. The length of the transcripts varied in a promoter-specific manner. Analysis of abortive products formed during the initiation showed that stronger promoters go to the elongation mode at transcript lengths shorter than that required for weaker promoters.

摘要

已知DNA超螺旋会影响原核生物中的基因表达模式。因此,转录起始机制与模板的拓扑状态密切相关。我们使用由纯化的RNA聚合酶和处于天然拓扑状态的启动子组成的体外重组转录分析方法,对T7早期启动子的转录起始进行了详细研究,包括以下步骤:三元复合物的形成、获得利福平抗性、σ因子的释放以及复合物中RNA链延伸的能力。我们确定了这些事件的顺序以及在超螺旋模板上转录起始过程中每个步骤发生时转录本的长度。转录本的长度以启动子特异性的方式变化。对起始过程中形成的流产产物的分析表明,较强的启动子在转录本长度短于较弱启动子所需长度时就进入延伸模式。

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