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复杂的枯草芽孢杆菌启动子RNA聚合酶结合位点的分离与分析

Separation and analysis of the RNA polymerase binding sites of a complex Bacillus subtilis promoter.

作者信息

Le Grice S F, Shih C C, Whipple F, Sonenshein A L

出版信息

Mol Gen Genet. 1986 Aug;204(2):229-36. doi: 10.1007/BF00425503.

Abstract

The Bacillus subtilis veg promotor site was shown to be composed of two neighboring RNA polymerase binding sites, only one of which ("Site I") produces a transcript. The relationship between these sites has been investigated following insertion of ten base pairs of DNA between the sites and subsequent cloning of each site independent of the other, and deletion of DNA sequences upstream from the productive site. The effect of DNA insertion was to permit transcription initiation from the previously nonproductive Site II, in either the presence or absence of Site I. This could be attributed to insertion of a purine residue seven base pairs downstream from the Pribnow box of Site II. Transcription from Site I was slightly increased in the presence of Site II in cis, but was still efficient in the absence of Site II, indicating that there is no absolute dependence on Site II for in vitro transcription from Site I.

摘要

枯草芽孢杆菌veg启动子位点由两个相邻的RNA聚合酶结合位点组成,其中只有一个位点(“位点I”)产生转录本。在两个位点之间插入10个碱基对的DNA,随后将每个位点独立于另一个位点进行克隆,并删除生产性位点上游的DNA序列后,对这些位点之间的关系进行了研究。DNA插入的作用是,无论位点I是否存在,都能使转录从前述非生产性的位点II起始。这可能归因于在位点II的普里布诺框下游7个碱基对处插入了一个嘌呤残基。在位点II顺式存在的情况下,位点I的转录略有增加,但在没有位点II的情况下仍然有效,这表明从位点I进行体外转录并不绝对依赖于位点II。

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