The Construction of Regulatory Network for Insulin-Mediated Genes by Integrating Methods Based on Transcription Factor Binding Motifs and Gene Expression Variations.
- Author:
Hyeim JUNG
1
;
Seonggyun HAN
;
Sangsoo KIM
Author Information
- Publication Type:Original Article
- Keywords: network; regulation; regulator; sequence motif
- MeSH: Biological Processes; Dataset; Diabetes Mellitus, Type 2; Gene Expression*; Humans; Insulin; Methods*; Muscle, Skeletal; Regulon; Transcription Factors*
- From:Genomics & Informatics 2015;13(3):76-80
- CountryRepublic of Korea
- Language:English
- Abstract: Type 2 diabetes mellitus is a complex metabolic disorder associated with multiple genetic, developmental and environmental factors. The recent advances in gene expression microarray technologies as well as network-based analysis methodologies provide groundbreaking opportunities to study type 2 diabetes mellitus. In the present study, we used previously published gene expression microarray datasets of human skeletal muscle samples collected from 20 insulin sensitive individuals before and after insulin treatment in order to construct insulin-mediated regulatory network. Based on a motif discovery method implemented by iRegulon, a Cytoscape app, we identified 25 candidate regulons, motifs of which were enriched among the promoters of 478 up-regulated genes and 82 down-regulated genes. We then looked for a hierarchical network of the candidate regulators, in such a way that the conditional combination of their expression changes may explain those of their target genes. Using Genomica, a software tool for regulatory network construction, we obtained a hierarchical network of eight regulons that were used to map insulin downstream signaling network. Taken together, the results illustrate the benefits of combining completely different methods such as motif-based regulatory factor discovery and expression level-based construction of regulatory network of their target genes in understanding insulin induced biological processes and signaling pathways.