Bucher P
Department of Polymer Research, Weizmann Institute of Science, Rehovot, Israel.
J Mol Biol. 1990 Apr 20;212(4):563-78. doi: 10.1016/0022-2836(90)90223-9.
Optimized weight matrices defining four major eukaryotic promoter elements, the TATA-box, cap signal, CCAAT-, and GC-box, are presented; they were derived by comparative sequence analysis of 502 unrelated RNA polymerase II promoter regions. The new TATA-box and cap signal descriptions differ in several respects from the only hitherto available base frequency Tables. The CCAAT-box matrix, obtained with no prior assumption but CCAAT being the core of the motif, reflects precisely the sequence specificity of the recently discovered nuclear factor NY-I/CP1 but does not include typical recognition sequences of two other purported CCAAT-binding proteins, CTF and CBP. The GC-box description is longer than the previously proposed consensus sequences but is consistent with Sp1 protein-DNA binding data. The notion of a CACCC element distinct from the GC-box seems not to be justified any longer in view of the new weight matrix. Unlike the two fixed-distance elements, neither the CCAAT- nor the GC-box occurs at significantly high frequency in the upstream regions of non-vertebrate genes. Preliminary attempts to predict promoters with the aid of the new signal descriptions were unexpectedly successful. The new TATA-box matrix locates eukaryotic transcription initiation sites as reliably as do the best currently available methods to map Escherichia coli promoters. This analysis was made possible by the recently established Eukaryotic Promoter Database (EPD) of the EMBL Nucleotide Sequence Data Library. In order to derive the weight matrices, a novel algorithm has been devised that is generally applicable to sequence motifs positionally correlated with a biologically defined position in the sequences. The signal must be sufficiently over-represented in a particular region relative to the given site, but need not be present in all members of the input sequence collection. The algorithm iteratively redefines the set of putative motif representatives from which a weight matrix is derived, so as to maximize a quantitative measure of local over-representation, an optimization criterion that naturally combines structural and positional constancy. A comprehensive description of the technique is presented in Methods and Data.
本文给出了定义四种主要真核生物启动子元件(TATA框、帽信号、CCAAT框和GC框)的优化权重矩阵;这些矩阵是通过对502个不相关的RNA聚合酶II启动子区域进行比较序列分析得出的。新的TATA框和帽信号描述在几个方面与目前唯一可用的碱基频率表不同。通过无先验假设但以CCAAT为基序核心得到的CCAAT框矩阵,精确反映了最近发现的核因子NY-I/CP1的序列特异性,但不包括另外两种所谓的CCAAT结合蛋白CTF和CBP的典型识别序列。GC框描述比先前提出的共有序列更长,但与Sp1蛋白-DNA结合数据一致。鉴于新的权重矩阵,与GC框不同的CACCC元件的概念似乎不再合理。与两个固定距离元件不同,CCAAT框和GC框在非脊椎动物基因的上游区域中出现的频率均不显著高。借助新的信号描述预测启动子的初步尝试意外地取得了成功。新的TATA框矩阵定位真核生物转录起始位点的可靠性与目前用于定位大肠杆菌启动子的最佳方法相当。这项分析得益于欧洲分子生物学实验室核苷酸序列数据库最近建立的真核生物启动子数据库(EPD)。为了得出权重矩阵,设计了一种新算法,该算法通常适用于与序列中生物学定义位置位置相关的序列基序。信号在相对于给定位点的特定区域中必须有足够的过度代表性,但不必存在于输入序列集合的所有成员中。该算法迭代地重新定义从中导出权重矩阵的假定基序代表集,以最大化局部过度代表性的定量度量,这是一种自然结合结构和位置恒定性的优化标准。方法和数据部分给出了该技术的全面描述。