Exploring the characteristics of sequence elements in proximal promoters of human genes

被引:18
作者
Bina, M [1 ]
Wyss, P
Ren, WH
Szpankowski, W
Thomas, E
Randhawa, R
Reddy, S
John, PM
Pares-Matos, EI
Stein, A
Xu, H
Lazarus, SA
机构
[1] Purdue Univ, Dept Chem, W Lafayette, IN 47907 USA
[2] Purdue Univ, Dept Comp Sci, W Lafayette, IN 47907 USA
[3] Cold Spring Harbor Lab, Watson Sch Biol Sci, Cold Spring Harbor, NY 11724 USA
[4] Purdue Univ, Dept Biol Sci, W Lafayette, IN 47907 USA
关键词
human genome; gene regulation; transcription factor binding sites; sequence context of human genomic DNA; codes in human DNA;
D O I
10.1016/j.ygeno.2004.08.013
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Central to reconstruction of cis-regulatory networks is identification and classification of naturally occurring transcription factor-binding sites according to the genes that they control. We have examined salient characteristics of 9-mers that occur in various orders and combinations in the proximal promoters of human genes. In evaluations of a dataset derived with respect to experimentally defined transcription initiation sites, in some cases we observed a clear correspondence of highly ranked 9-mers with protein-binding sites in genomic DNA. Evaluations of the larger dataset, derived with respect to the 5'-end of human ESTs, revealed that a subset of the highly ranked 9-mers corresponded to sites for several known transcription factor families (including CREB, ETS, EGR-1, SP1, KLF, MAZ, HIF-1, and STATs) that play important roles in the regulation of vertebrate genes. We identified several highly ranked CpG-containing 9-mers, defining sites for interactions with the CREB and ETS families of proteins, and identified potential target genes for these proteins. The results of the studies imply that the CpG-containing transcription factor-binding sites regulate the expression of genes with important roles in pathways leading to cell-type-specific gene expression and pathways controlled by the complex networks of signaling systems. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:929 / 940
页数:12
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