Understanding Epistatic Interactions between Genes Targeted by Non-coding Regulatory Elements in Complex Diseases.
- Author:
Min Kyung SUNG
1
;
Hyoeun BANG
;
Jung Kyoon CHOI
Author Information
- Publication Type:Original Article
- Keywords: coronary artery disease; diabetes mellitus; epistasis; hypertension; regulatory region
- MeSH: Coronary Artery Disease; Deoxyribonuclease I; Diabetes Mellitus; Diabetes Mellitus, Type 2; DNA; Gene Expression; Genome-Wide Association Study; Hypertension; Korea; Polymorphism, Single Nucleotide; Regulatory Sequences, Nucleic Acid; Transcription Factors
- From:Genomics & Informatics 2014;12(4):181-186
- CountryRepublic of Korea
- Language:English
- Abstract: Genome-wide association studies have proven the highly polygenic architecture of complex diseases or traits; therefore, single-locus-based methods are usually unable to detect all involved loci, especially when individual loci exert small effects. Moreover, the majority of associated single-nucleotide polymorphisms resides in non-coding regions, making it difficult to understand their phenotypic contribution. In this work, we studied epistatic interactions associated with three common diseases using Korea Association Resource (KARE) data: type 2 diabetes mellitus (DM), hypertension (HT), and coronary artery disease (CAD). We showed that epistatic single-nucleotide polymorphisms (SNPs) were enriched in enhancers, as well as in DNase I footprints (the Encyclopedia of DNA Elements [ENCODE] Project Consortium 2012), which suggested that the disruption of the regulatory regions where transcription factors bind may be involved in the disease mechanism. Accordingly, to identify the genes affected by the SNPs, we employed whole-genome multiple-cell-type enhancer data which discovered using DNase I profiles and Cap Analysis Gene Expression (CAGE). Assigned genes were significantly enriched in known disease associated gene sets, which were explored based on the literature, suggesting that this approach is useful for detecting relevant affected genes. In our knowledge-based epistatic network, the three diseases share many associated genes and are also closely related with each other through many epistatic interactions. These findings elucidate the genetic basis of the close relationship between DM, HT, and CAD.
