DNA Supercoiling, Topoisomerases, and Cohesin: Partners in Regulating Chromatin Architecture?

Int J Mol Sci. 2018 Mar 16;19(3):884. doi: 10.3390/ijms19030884.

Abstract

Although our knowledge of chromatin organization has advanced significantly in recent years, much about the relationships between different features of genome architecture is still unknown. Folding of mammalian genomes into spatial domains is thought to depend on architectural proteins, other DNA-binding proteins, and different forms of RNA. In addition, emerging evidence points towards the possibility that the three-dimensional organisation of the genome is controlled by DNA topology. In this scenario, cohesin, CCCTC-binding factor (CTCF), transcription, DNA supercoiling, and topoisomerases are integrated to dictate different layers of genome organization, and the contribution of all four to gene control is an important direction of future studies. In this perspective, we review recent studies that give new insight on how DNA supercoiling shape chromatin structure.

Keywords: CTCF; DNA topology; cohesin; genome organization; topoisomerase; transcription.

Publication types

  • Review

MeSH terms

  • Animals
  • CCCTC-Binding Factor / chemistry
  • CCCTC-Binding Factor / metabolism
  • Cell Cycle Proteins / chemistry*
  • Cell Cycle Proteins / metabolism
  • Chromatin / chemistry*
  • Chromatin / metabolism
  • Chromosomal Proteins, Non-Histone / chemistry*
  • Chromosomal Proteins, Non-Histone / metabolism
  • Cohesins
  • DNA Topoisomerases / chemistry*
  • DNA Topoisomerases / metabolism
  • DNA, Superhelical / chemistry*
  • DNA, Superhelical / metabolism
  • Genome
  • Humans
  • Nucleic Acid Conformation*
  • RNA / chemistry
  • RNA / metabolism
  • Transcription, Genetic

Substances

  • CCCTC-Binding Factor
  • CTCF protein, human
  • Cell Cycle Proteins
  • Chromatin
  • Chromosomal Proteins, Non-Histone
  • DNA, Superhelical
  • RNA
  • DNA Topoisomerases