iRegNet3D: three-dimensional integrated regulatory network for the genomic analysis of coding and non-coding disease mutations

Genome Biol. 2017 Jan 18;18(1):10. doi: 10.1186/s13059-016-1138-2.

Abstract

The mechanistic details of most disease-causing mutations remain poorly explored within the context of regulatory networks. We present a high-resolution three-dimensional integrated regulatory network (iRegNet3D) in the form of a web tool, where we resolve the interfaces of all known transcription factor (TF)-TF, TF-DNA and chromatin-chromatin interactions for the analysis of both coding and non-coding disease-associated mutations to obtain mechanistic insights into their functional impact. Using iRegNet3D, we find that disease-associated mutations may perturb the regulatory network through diverse mechanisms including chromatin looping. iRegNet3D promises to be an indispensable tool in large-scale sequencing and disease association studies.

Keywords: Chromatin interaction network; Disease-associated mutation; Inherited disease; Missense mutation; Non-coding mutation; TF-DNA interaction network; TF-TF interaction network; Transcriptional regulation; iRegNet3D.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Binding Sites
  • Chromatin / genetics
  • Chromatin / metabolism
  • DNA / chemistry
  • DNA / metabolism
  • DNA-Binding Proteins / chemistry
  • DNA-Binding Proteins / metabolism
  • Epistasis, Genetic
  • Gene Expression Regulation
  • Gene Regulatory Networks*
  • Genetic Predisposition to Disease*
  • Genome-Wide Association Study / methods*
  • Genomics / methods*
  • Humans
  • Models, Molecular*
  • Mutation*
  • Nucleotide Motifs
  • Open Reading Frames
  • Quantitative Structure-Activity Relationship*
  • Transcription Factors / chemistry
  • Transcription Factors / metabolism
  • Untranslated Regions

Substances

  • Chromatin
  • DNA-Binding Proteins
  • Transcription Factors
  • Untranslated Regions
  • DNA