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通过实验确定的启动子起始子和TBP结合位点元件的权重矩阵定义。

Experimentally determined weight matrix definitions of the initiator and TBP binding site elements of promoters.

作者信息

Kraus R J, Murray E E, Wiley S R, Zink N M, Loritz K, Gelembiuk G W, Mertz J E

机构信息

McArdle Laboratory for Cancer Research, University of Wisconsin Medical School, Madison 53706-1599, USA.

出版信息

Nucleic Acids Res. 1996 Apr 15;24(8):1531-9. doi: 10.1093/nar/24.8.1531.

Abstract

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.

摘要

II类启动子的基本元件包括:(i)-30区域,可被TATA结合蛋白(TBP)识别;(ii)围绕转录起始位点的起始子(Inr);(iii)通常还有一个下游(+10至+35)元件。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。在体内和体外分别测定了每个突变体的转录活性。结果发现,在体内和体外,转录活性与与最佳Inr序列5'-CAG/TT-3'的契合度之间都存在极好的相关性。利用神经网络技术,我们根据这些数据生成了一个Inr的权重矩阵定义,可用于预测给定序列作为Inr的活性。同样,利用TBP结合位点的饱和诱变数据,我们生成了-30区域元件的权重矩阵定义。我们得出以下结论:(i)Inr由紧邻转录起始位点的核苷酸定义;(ii)大多数(如果不是全部)Inr被相同的通用转录因子识别。我们提出,转录起始机制在根本上是保守的,预起始复合物的形成涉及通用转录因子同时结合到II类启动子的-30、Inr以及可能的下游元件。

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