A systematic model to predict transcriptional regulatory mechanisms based on over representation of transcription factor binding profiles

被引:55
作者
Chang, LW
Nagarajan, R
Magee, JA
Milbrandt, J
Stormo, GD [1 ]
机构
[1] Washington Univ, Sch Med, Dept Genet, St Louis, MO 63110 USA
[2] Washington Univ, Dept Biomed Engn, St Louis, MO 63130 USA
[3] Washington Univ, Sch Med, Div Lab Med, Dept Pathol & Immunol, St Louis, MO 63110 USA
关键词
D O I
10.1101/gr.4303406
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
An important aspect Of understanding a biological pathway is to delineate the transcriptional regulatory mechanisms of the genes involved. Two important tasks are often encountered when studying transcription regulation, i.e., (1) the identification of common transcriptional regulators of a set of coexpressed genes; (2) the identification of genes that are regulated by one or several transcription factors. In this Study, a systematic and statistical approach was taken to accomplish these tasks by establishing an integrated model considering all of the promoters and characterized transcription factors (TFs) in the genome. A promoter analysis pipeline (PAP) was developed to implement this approach. PAP was tested using coregulated gene clusters collected from the literature. In most test cases, PAP identified the transcription regulators of the input genes accurately. When compared with chromatin immunoprecipitation experiment data, PAP's predictions are consistent with the experimental observations. When PAP was used to analyze one published expression-profiling data set and two novel coregulated gene sets, PAP was able to generate biologically meaningful hypotheses. Therefore, by taking a systematic approach of considering all promoters and characterized TFs in our model, we were able to make more reliable predictions about the regulation of gene expression in mammalian organisms.
引用
收藏
页码:405 / 413
页数:9
相关论文
共 51 条
[1]   Toucan:: deciphering the cis-regulatory logic of coregulated genes [J].
Aerts, S ;
Thijs, G ;
Coessens, B ;
Staes, M ;
Moreau, Y ;
Moor, BD .
NUCLEIC ACIDS RESEARCH, 2003, 31 (06) :1753-1764
[2]   Environmentally induced foregut remodeling by PHA-4/FoxA and DAF-12/NHR [J].
Ao, W ;
Gaudet, J ;
Kent, WJ ;
Muttumu, S ;
Mango, SE .
SCIENCE, 2004, 305 (5691) :1743-1746
[3]   NF-κB as a frequent target for immunosuppressive and anti-inflammatory molecules [J].
Baeuerle, PA ;
Baichwal, VR .
ADVANCES IN IMMUNOLOGY, VOL 65, 1997, 65 :111-137
[4]   SELECTION OF DNA-BINDING SITES BY REGULATORY PROTEINS - STATISTICAL-MECHANICAL THEORY AND APPLICATION TO OPERATORS AND PROMOTERS [J].
BERG, OG ;
VONHIPPEL, PH .
JOURNAL OF MOLECULAR BIOLOGY, 1987, 193 (04) :723-743
[5]   Aligning multiple genomic sequences with the threaded blockset aligner [J].
Blanchette, M ;
Kent, WJ ;
Riemer, C ;
Elnitski, L ;
Smit, AFA ;
Roskin, KM ;
Baertsch, R ;
Rosenbloom, K ;
Clawson, H ;
Green, ED ;
Haussler, D ;
Miller, W .
GENOME RESEARCH, 2004, 14 (04) :708-715
[6]   Discovery of regulatory elements by a computational method for phylogenetic footprinting [J].
Blanchette, M ;
Tompa, M .
GENOME RESEARCH, 2002, 12 (05) :739-748
[7]   Inferring combinatorial regulation of transcription in silico [J].
Blüthgen, N ;
Kielbasa, SM ;
Herzel, H .
NUCLEIC ACIDS RESEARCH, 2005, 33 (01) :272-279
[8]   Gene expression signature of fibroblast serum response predicts human cancer progression: Similarities between tumors and wounds [J].
Chang, HY ;
Sneddon, JB ;
Alizadeh, AA ;
Sood, R ;
West, RB ;
Montgomery, K ;
Chi, JT ;
van de Rijn, M ;
Botstein, D ;
Brown, PO .
PLOS BIOLOGY, 2004, 2 (02) :206-214
[9]   Expression-based monitoring of transcription factor activity: the TELiS database [J].
Cole, SW ;
Yan, W ;
Galic, Z ;
Arevalo, J ;
Zack, JA .
BIOINFORMATICS, 2005, 21 (06) :803-810
[10]   Integrating high-throughput and computational data elucidates bacterial networks [J].
Covert, MW ;
Knight, EM ;
Reed, JL ;
Herrgard, MJ ;
Palsson, BO .
NATURE, 2004, 429 (6987) :92-96