Weight matrix descriptions of four eukaryotic RNA polymerase II promoter elements derived from 502 unrelated promoter sequences

CAAT箱 塔塔盒子 发起人 共识序列 生物 抄写(语言学) 遗传学 RNA聚合酶 基因 计算生物学 核糖核酸 基因表达 肽序列 语言学 哲学
作者
Philipp Bücher
出处
期刊:Journal of Molecular Biology [Elsevier]
卷期号:212 (4): 563-578 被引量:1084
标识
DOI:10.1016/0022-2836(90)90223-9
摘要

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.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
好难啊发布了新的文献求助10
1秒前
1秒前
5秒前
6秒前
6秒前
wewe完成签到,获得积分20
7秒前
李大爷发布了新的文献求助10
7秒前
Kevin完成签到,获得积分10
9秒前
酷炫的尔丝完成签到 ,获得积分10
9秒前
Hello应助标致的蛋挞采纳,获得50
10秒前
大个应助明亮的宁采纳,获得10
11秒前
Rainbow发布了新的文献求助10
11秒前
anyone发布了新的文献求助30
12秒前
充电宝应助SY采纳,获得10
13秒前
D先生完成签到,获得积分20
13秒前
yxt完成签到,获得积分10
13秒前
momo发布了新的文献求助10
14秒前
16秒前
苏照杭应助长度2到采纳,获得10
16秒前
17秒前
次我完成签到,获得积分10
17秒前
qisili关注了科研通微信公众号
18秒前
Owen应助李大爷采纳,获得10
19秒前
20秒前
脑洞疼应助迅速冰岚采纳,获得10
22秒前
NexusExplorer应助whoops采纳,获得10
22秒前
sweetbearm应助通~采纳,获得10
22秒前
VDC应助欢呼冰岚采纳,获得30
22秒前
Grayball应助hhl采纳,获得10
22秒前
充电宝应助次我采纳,获得10
23秒前
sgjj33发布了新的文献求助10
24秒前
墨墨完成签到,获得积分10
25秒前
蒸馏水完成签到,获得积分10
25秒前
123完成签到,获得积分10
25秒前
李大爷完成签到,获得积分10
26秒前
SY发布了新的文献求助10
26秒前
journey完成签到 ,获得积分10
30秒前
kaw发布了新的文献求助10
30秒前
彭于晏应助hdd采纳,获得10
33秒前
感性的寄真完成签到 ,获得积分10
33秒前
高分求助中
Continuum Thermodynamics and Material Modelling 3000
Production Logging: Theoretical and Interpretive Elements 2700
Ensartinib (Ensacove) for Non-Small Cell Lung Cancer 1000
Unseen Mendieta: The Unpublished Works of Ana Mendieta 1000
Bacterial collagenases and their clinical applications 800
El viaje de una vida: Memorias de María Lecea 800
Luis Lacasa - Sobre esto y aquello 700
热门求助领域 (近24小时)
化学 材料科学 生物 医学 工程类 有机化学 生物化学 物理 纳米技术 计算机科学 内科学 化学工程 复合材料 基因 遗传学 物理化学 催化作用 量子力学 光电子学 冶金
热门帖子
关注 科研通微信公众号,转发送积分 3528035
求助须知:如何正确求助?哪些是违规求助? 3108306
关于积分的说明 9288252
捐赠科研通 2805909
什么是DOI,文献DOI怎么找? 1540220
邀请新用户注册赠送积分活动 716950
科研通“疑难数据库(出版商)”最低求助积分说明 709851