Allegro: Analyzing expression and sequence in concert to discover regulatory programs

被引:30
作者
Halperin, Yonit [1 ]
Linhart, Chaim [1 ]
Ulitsky, Igor [1 ]
Shamir, Ron [1 ]
机构
[1] Tel Aviv Univ, Sch Comp Sci, IL-69978 Tel Aviv, Israel
基金
以色列科学基金会;
关键词
CELL-CYCLE ARREST; TRANSCRIPTION-FACTOR; GENE-EXPRESSION; SACCHAROMYCES-CEREVISIAE; MOTIF DISCOVERY; BINDING SITES; CREB GENE; IDENTIFICATION; MOUSE; NETWORK;
D O I
10.1093/nar/gkn1064
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
A major goal of system biology is the characterization of transcription factors and microRNAs (miRNAs) and the transcriptional programs they regulate. We present Allegro, a method for de-novo discovery of cis-regulatory transcriptional programs through joint analysis of genome-wide expression data and promoter or 3 UTR sequences. The algorithm uses a novel log-likelihood-based, non-parametric model to describe the expression pattern shared by a group of co-regulated genes. We show that Allegro is more accurate and sensitive than existing techniques, and can simultaneously analyze multiple expression datasets with more than 100 conditions. We apply Allegro on datasets from several species and report on the transcriptional modules it uncovers. Our analysis reveals a novel motif over-represented in the promoters of genes highly expressed in murine oocytes, and several new motifs related to fly development. Finally, using stem-cell expression profiles, we identify three miRNA families with pivotal roles in human embryogenesis.
引用
收藏
页码:1566 / 1579
页数:14
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