3D genome and its disorganization in diseases

Cell Biol Toxicol. 2018 Oct;34(5):351-365. doi: 10.1007/s10565-018-9430-4. Epub 2018 May 23.

Abstract

The chromosomes in eukaryotic cells are highly folded and organized to form dynamic three-dimensional (3D) structures. In recent years, many technologies including chromosome conformation capture (3C) and 3C-based technologies (Hi-C, ChIA-PET) have been developed to investigate the 3D structure of chromosomes. These technologies are enabling research on how gene regulatory events are affected by the 3D genome structure, which is increasingly implicated in the regulation of gene expression and cellular functions. Importantly, many diseases are associated with genetic variations, most of which are located in non-coding regions. However, it is difficult to determine the mechanisms by which these variations lead to diseases. With 3D genome technologies, we can now better determine the consequences of non-coding genome alterations via their impact on chromatin interactions and structures in cancer and other diseases. In this review, we introduce the various 3D genome technologies, with a focus on their application to cancer and disease research, as well as future developments to extend their utility.

Keywords: 3D genome; Cancer; Disease; Hi-C.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Chromatin / genetics
  • Chromatin / physiology
  • Chromosome Structures / genetics*
  • Chromosome Structures / physiology*
  • Chromosomes / genetics
  • Computational Biology / methods
  • DNA / metabolism
  • DNA Breaks, Double-Stranded
  • Disease / genetics
  • Genome / physiology
  • Genomic Instability / genetics*
  • Genomic Instability / physiology
  • Humans
  • Imaging, Three-Dimensional / methods
  • Sequence Analysis, DNA / methods
  • Syndrome

Substances

  • Chromatin
  • DNA