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Synergy of human Pol II core promoter elements revealed by statistical sequence analysis

机译:统计序列分析揭示人Pol II核心启动子元件的协同作用

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Motivation: The subject of our paper is bioinformatics analysis of the distinguishing features of human promoter DNA sequences, in particular of synergetic combinations of core promoter elements therein. We suppose that specific scenarios of transcription initiation are essentially related to various particular implementations of the interaction of basal transcription machinery with promoter DNA, depending on the presence and mutual positioning of core promoter elements.Results: In addition to the combinations of core promoter elements previously experimentally confirmed [TATA box and Initiator (Inr), Downstream Promoter Element (DPE) and Inr, and TFIIB recognition element (BRE) and TATA box] we propose other alternate synergetic combinations: BRE and Inr, BRE and DPE, and TATA and DPE with respective models. The suggestion is based on a high statistical significance of the alternate combinations in promoters, comparable with the significance of the known combinations. We also present arguments that the BRE element is statistically more important than previously thought, and suggest possible mechanisms of action of the core elements in the promoters with multiple transcription start sites.
机译:动机:本文的主题是生物信息学分析人类启动子DNA序列的独特特征,特别是其中的核心启动子元件的协同组合。我们假设转录启动的具体情况基本上取决于基础转录机制与启动子DNA相互作用的各种特定实现方式,这取决于核心启动子元件的存在和相互定位。结果:除了以前核心启动子元件的组合之外经过实验确认[TATA盒和引发剂(Inr),下游启动子元素(DPE)和Inr,以及TFIIB识别元素(BRE)和TATA盒],我们提出了其他替代的协同组合:BRE和Inr,BRE和DPE,以及TATA和DPE与各自的模型。该建议是基于启动子中替代组合的高统计意义,与已知组合的意义相当。我们还提出论点,即BRE元素在统计学上比以前认为的要重要,并提出了具有多个转录起始位点的启动子中核心元素可能的作用机制。

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