Transcriptional network dynamics in macrophage activation

被引:95
作者
Nilsson, Roland
Bajic, Vladimir B.
Suzuki, Harukazu
di Bernardo, Diego
Bjorkegren, Johan
Katayama, Shintaro
Reid, James F.
Sweet, Matthew J.
Gariboldi, Manuela
Carninci, Piero
Hayashizaki, Yosihide
Hume, David A.
Tegner, Jesper
Ravasi, Timothy
机构
[1] Univ Calif San Diego, Dept Bioengn, Jacobs Sch Engn, La Jolla, CA 92093 USA
[2] Karolinska Inst, Ctr Genom & Bioinformat, Stockholm, Sweden
[3] Linkoping Univ, IFM, S-58183 Linkoping, Sweden
[4] Inst Infocomm Res, Knowledge Extract Lab, Singapore 119613, Singapore
[5] Univ Western Cape, ZA-7535 Bellville, South Africa
[6] RIKEN Genom Sci Ctr, Genome Explorat Res Grp, RIKEN Yokohama Inst, Tsurumi Ku, Yokohama, Kanagawa 2300045, Japan
[7] Telethon Inst Genet & Med, Naples, Italy
[8] Ist Nazl Studio & Cura Tumori, Dept Expt Oncol, I-20133 Milan, Italy
[9] Univ Queensland, ARC Special Res Ctr Funct & Appl Genom, Inst Mol Biosci, Brisbane, Qld 4072, Australia
[10] RIKEN, Wako Inst, Genome Sci Lab, Discovery Res Inst, Wako, Saitama 3510198, Japan
关键词
system biology; regulatory networks; network dynamics; complex systems; transcriptional regulation; genome; macrophages; innate immunity; inflammation;
D O I
10.1016/j.ygeno.2006.03.022
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
Transcriptional regulatory networks govern cell differentiation and the cellular response to external stimuli. However, mammalian model systems have not yet been accessible for network analysis. Here, we present a genome-wide network analysis of the transcriptional regulation underlying the mouse macrophage response to bacterial lipopolysaccharide (LPS). Key to uncovering the network structure is our combination of time-series cap analysis of gene expression with in silico prediction of transcription factor binding sites. By integrating microarray and qPCR time-series expression data with a promoter analysis, we find dynamic subnetworks that describe how signaling pathways change dynamically during the progress of the macrophage LPS response, thus defining regulatory modules characteristic of the inflammatory response. In particular, our integrative analysis enabled us to suggest novel roles for the transcription factors ATF-3 and NRF-2 during the inflammatory response. We believe that our system approach presented here is applicable to understanding cellular differentiation in higher eukaryotes. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:133 / 142
页数:10
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