Technologies to study spatial genome organization: beyond 3C

Brief Funct Genomics. 2019 Nov 19;18(6):395-401. doi: 10.1093/bfgp/elz019.

Abstract

The way that chromatin is organized in three-dimensional nuclear space is now acknowledged as a factor critical for the major cell processes, like transcription, replication and cell division. Researchers have been armed with new molecular and imaging technologies to study this structure-to-function link of genomes, spearheaded by the introduction of the 'chromosome conformation capture' technology more than a decade ago. However, this technology is not without shortcomings, and novel variants and orthogonal approaches are being developed to overcome these. As a result, the field of nuclear organization is constantly fueled by methods of increasing resolution and/or throughput that strive to eliminate systematic biases and increase precision. In this review, we attempt to highlight the most recent advances in technology that promise to provide novel insights on how chromosomes fold and function.

Keywords: chromatin folding; chromosome conformation capture; nuclear body; single-cell analysis; super-resolution/high-throughput microscopy; territory.

Publication types

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

MeSH terms

  • Animals
  • Cell Nucleus / metabolism
  • Chromatin / chemistry
  • Chromatin / metabolism
  • Chromosomes / chemistry
  • Chromosomes / metabolism
  • Genome / physiology*
  • Humans
  • Molecular Conformation
  • Molecular Imaging / methods*
  • Nucleic Acid Conformation*

Substances

  • Chromatin