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大肠杆菌RNA聚合酶转录起始的体外研究。3. 启动子识别区域内单个DNA元件对流产起始和启动子逃逸的影响。

In vitro studies of transcript initiation by Escherichia coli RNA polymerase. 3. Influences of individual DNA elements within the promoter recognition region on abortive initiation and promoter escape.

作者信息

Vo Nam V, Hsu Lilian M, Kane Caroline M, Chamberlin Michael J

机构信息

Division of Biochemistry and Molecular Biology, Department of Molecular and Cell Biology, University of California, Berkeley, California 94720-3202, USA.

出版信息

Biochemistry. 2003 Apr 8;42(13):3798-811. doi: 10.1021/bi026962v.

Abstract

Abortive initiation and promoter escape are two principal biochemical reactions occurring in the latter stage of transcript initiation. We have analyzed the influences of individual DNA elements within the promoter recognition region (PRR) on these reactions by measuring the quantitative initiation parameters that describe abortive initiation and promoter escape; these parameters are the abortive rate, the productive rate, the abortive:productive ratio, the abortive probability, and the maximum size of abortive transcripts. Changes in the individual DNA elements within the PRR can have a substantial effect on each of these parameters. The discriminator region and the -10 element primarily influence the abortive probability at positions 2-5 and 6-10, respectively, while the -10 and -35 conserved hexamers and the spacer region affect the abortive probability at positions 11-15. Surprisingly, transcription of a consensus promoter invariably gives a higher abortive yield, a higher abortive probability, a longer abortive ladder, and a lower productive rate than promoter variants carrying even a single deviation in the consensus hexamers. These results suggest that strong RNA polymerase-PRR interactions stall the polymerase at the promoter, thereby reducing the rate of promoter escape and consequently enhancing the extent of abortive initiation.

摘要

流产起始和启动子逃逸是转录起始后期发生的两个主要生化反应。我们通过测量描述流产起始和启动子逃逸的定量起始参数,分析了启动子识别区域(PRR)内单个DNA元件对这些反应的影响;这些参数是流产率、产率、流产与产率之比、流产概率以及流产转录本的最大长度。PRR内单个DNA元件的变化会对这些参数中的每一个产生实质性影响。鉴别区域和-10元件分别主要影响第2至5位和第6至10位的流产概率,而-10和-35保守六聚体以及间隔区域影响第11至15位的流产概率。令人惊讶的是,与在保守六聚体中甚至有一个偏差的启动子变体相比,共有启动子的转录总是产生更高的流产产量、更高的流产概率、更长的流产梯状产物以及更低的产率。这些结果表明,强烈的RNA聚合酶与PRR相互作用使聚合酶在启动子处停滞,从而降低启动子逃逸率,进而提高流产起始的程度。

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