학술논문

Discovery of Novel Human Gene Regulatory Modules from Gene Co-expression and Promoter Motif Analysis.
Document Type
article
Source
Scientific reports. 7(1)
Subject
Humans
Lysine
CCAAT-Binding Factor
Oligonucleotide Array Sequence Analysis
Gene Expression Regulation
Epigenesis
Genetic
Methylation
Sp1 Transcription Factor
Interferon Regulatory Factor-1
YY1 Transcription Factor
Gene Regulatory Networks
Promoter Regions
Genetic
Nucleotide Motifs
Regulatory Factor X1
Genetics
Human Genome
Biotechnology
2.1 Biological and endogenous factors
Generic Health Relevance
Epigenesis
Genetic
Promoter Regions
Biochemistry and Cell Biology
Other Physical Sciences
Language
Abstract
Deciphering gene regulatory networks requires identification of gene expression modules. We describe a novel bottom-up approach to identify gene modules regulated by cis-regulatory motifs from a human gene co-expression network. Target genes of a cis-regulatory motif were identified from the network via the motif's enrichment or biased distribution towards transcription start sites in the promoters of co-expressed genes. A gene sub-network containing the target genes was extracted and used to derive gene modules. The analysis revealed known and novel gene modules regulated by the NF-Y motif. The binding of NF-Y proteins to these modules' gene promoters were verified using ENCODE ChIP-Seq data. The analyses also identified 8,048 Sp1 motif target genes, interestingly many of which were not detected by ENCODE ChIP-Seq. These target genes assemble into house-keeping, tissues-specific developmental, and immune response modules. Integration of Sp1 modules with genomic and epigenomic data indicates epigenetic control of Sp1 targets' expression in a cell/tissue specific manner. Finally, known and novel target genes and modules regulated by the YY1, RFX1, IRF1, and 34 other motifs were also identified. The study described here provides a valuable resource to understand transcriptional regulation of various human developmental, disease, or immunity pathways.