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大肠杆菌RNA聚合酶的转录暂停受下游DNA序列调控。

Transcription pausing by Escherichia coli RNA polymerase is modulated by downstream DNA sequences.

作者信息

Lee D N, Phung L, Stewart J, Landick R

机构信息

Department of Biology, Washington University, St. Louis, Missouri 63130.

出版信息

J Biol Chem. 1990 Sep 5;265(25):15145-53.

PMID:1697586
Abstract

Escherichia coli RNA polymerase pauses immediately after transcription of certain sequences that can form stable secondary structures in the nascent RNA transcript; pausing appears to be essential for several types of bacterial transcription attenuation mechanisms. Because base changes that weaken the RNA secondary structures reduce the half-life of pausing by RNA polymerase, nascent transcript RNA hairpins are thought to cause pausing at these sites. We show here that, for the well characterized trpL pause site, the determinants of transcription pausing are not limited to the RNA hairpin, but include the not-yet-transcribed sequence of DNA immediately downstream from the pause site. We show that this effect extends to bases up to fourteen nucleotides downstream from the pause site, that placement of a oligo(dT) tract in the nontranscribed strand in this region does not convert the pause site to a termination site, and that shifting the position of pausing by one nucleotide downstream almost eliminates pausing. From an analysis of many variants of this downstream sequence, we argue that the effect of downstream sequence is not related simply to its GC content. We suggest that these effects are mediated by altered interactions between RNA polymerase and the DNA template downstream from the enzyme's active site.

摘要

大肠杆菌RNA聚合酶在转录某些能在新生RNA转录本中形成稳定二级结构的序列后会立即暂停;暂停似乎对几种类型的细菌转录衰减机制至关重要。由于削弱RNA二级结构的碱基变化会缩短RNA聚合酶暂停的半衰期,因此新生转录本RNA发夹结构被认为会导致在这些位点暂停。我们在此表明,对于特征明确的trpL暂停位点,转录暂停的决定因素不仅限于RNA发夹结构,还包括紧邻暂停位点下游尚未转录的DNA序列。我们表明这种效应延伸到暂停位点下游多达14个核苷酸的碱基,在该区域非转录链中放置一段寡聚(dT)序列不会将暂停位点转变为终止位点,并且将暂停位置向下游移动一个核苷酸几乎会消除暂停。通过对该下游序列的许多变体进行分析,我们认为下游序列的效应并非简单地与其GC含量相关。我们认为这些效应是由RNA聚合酶与该酶活性位点下游的DNA模板之间相互作用的改变所介导的。

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