A systems biology approach to understanding cis-regulatory module function

被引:30
|
作者
Jeziorska, Danuta M.
Jordan, Kate W.
Vance, Keith W. [1 ]
机构
[1] Univ Warwick, Dept Syst Biol, Biomed Res Inst, Coventry CV4 7AL, W Midlands, England
关键词
cis-Regulatory module; Transcription; Chromatin; Gene regulatory networks; Imaging; EMBRYONIC STEM-CELLS; CONSERVED NONCODING SEQUENCES; GENOME-SCALE IDENTIFICATION; BETA-GLOBIN LOCUS; GENE-EXPRESSION; CHROMOSOME CONFORMATION; TRANSCRIPTIONAL ENHANCERS; DROSOPHILA-MELANOGASTER; CHROMATIN ORGANIZATION; NUCLEAR ARCHITECTURE;
D O I
10.1016/j.semcdb.2009.07.007
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The genomic instructions used to regulate development are encoded within a set of functional DNA elements called cis-regulatory modules (CRMs). These elements determine the precise patterns of temporal and spatial gene expression. Here we summarize recent progress made towards cataloguing and characterizing the complete repertoire of CRMs. We describe CRMs as genomic information processing devices containing clusters of transcription factor binding sites and we position CRMs as nodes within large gene regulatory networks. We define CRM architecture and describe how these genomic elements process the information they encode to their target genes. Furthermore, we present an overview describing high-throughput techniques to identify CRMs genome wide and experimental methodologies to validate their function on a large scale. This review emphasizes the advantages and power of a systems biology approach which integrates computational and experimental technologies to further our understanding of CRM function. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:856 / 862
页数:7
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