首页> 外文期刊>Nucleic Acids Research >EXPERIMENTALLY DETERMINED WEIGHT MATRIX DEFINITIONS OF THE INITIATOR AND TBP BINDING SITE ELEMENTS OF PROMOTERS
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EXPERIMENTALLY DETERMINED WEIGHT MATRIX DEFINITIONS OF THE INITIATOR AND TBP BINDING SITE ELEMENTS OF PROMOTERS

机译:实验确定的启动子的重量矩阵定义和启动子的TBP结合位元

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摘要

The basal elements of class II promoters are: (i) a-30 region, recognized by TATA binding protein (TBP); (ii) an initiator (Inr) surrounding the start site for transcription; (iii) frequently a downstream (+10 to +35) element, To determine the sequences that specify an Inr, we performed a saturation mutagenesis of the Inr of the SV40 major late promoter (SV40-MLP). The transcriptional activity of each mutant was determined both in vivo and in vitro. An excellent correlation between transcriptional activity and closeness of fit to the optimal Inr sequence, 5'-CAG/TT-3', was found to exist both in vivo and in vitro, Employing a neural network technique we generated from these data a weight matrix definition of an Inr that can be used to predict the activity of a given sequence as an Inr, Using saturation mutagenesis data of TBP binding sites we likewise generated a weight matrix definition of the -30 region element, We conclude the following: (i) Inrs are defined by the nucleotides immediately surrounding the transcriptional start site; (ii) most, if not all, Inrs are recognized by the same general transcription factor(s), We propose that the mechanism of transcription initiation is fundamentally conserved, with the formation of pre-initiation complexes involving the concurrent binding of general transcription factors to the -30, Inr and, possibly, downstream elements of class II promoters.
机译:II类启动子的基础元件是:(i)被TATA结合蛋白(TBP)识别的a-30区; (ii)围绕起始位点进行转录的引发剂(Inr); (iii)通常是下游(+10至+35)元素,为了确定指定Inr的序列,我们对SV40主要晚期启动子(SV40-MLP)的Inr进行了饱和诱变。在体内和体外都确定了每种突变体的转录活性。发现转录活性和与最佳Inr序列5'-CAG / TT-3'的拟合紧密度之间存在极好的相关性,这是利用我们从这些数据生成的神经网络技术建立的重量矩阵可以用来预测给定序列作为Inr的活性的Inr的定义,使用TBP结合位点的饱和诱变数据,我们同样生成了-30区域元素的权重矩阵定义,我们得出以下结论:(i) Inrs由紧邻转录起始位点的核苷酸定义; (ii)大部分(如果不是全部)Inrs被相同的通用转录因子识别,我们建议转录起始机制是基本保守的,形成涉及通用转录因子同时结合的起始前复合物II类启动子的-30,Inr和可能的下游元件。

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