Topoisomerase IIα represses transcription by enforcing promoter-proximal pausing

Cell Rep. 2021 Apr 13;35(2):108977. doi: 10.1016/j.celrep.2021.108977.

Abstract

Accumulation of topological stress in the form of DNA supercoiling is inherent to the advance of RNA polymerase II (Pol II) and needs to be resolved by DNA topoisomerases to sustain productive transcriptional elongation. Topoisomerases are therefore considered positive facilitators of transcription. Here, we show that, in contrast to this general assumption, human topoisomerase IIα (TOP2A) activity at promoters represses transcription of immediate early genes such as c-FOS, maintaining them under basal repressed conditions. Thus, TOP2A inhibition creates a particular topological context that results in rapid release from promoter-proximal pausing and transcriptional upregulation, which mimics the typical bursting behavior of these genes in response to physiological stimulus. We therefore describe the control of promoter-proximal pausing by TOP2A as a layer for the regulation of gene expression, which can act as a molecular switch to rapidly activate transcription, possibly by regulating the accumulation of DNA supercoiling at promoter regions.

Keywords: DNA supercoiling; DNA topoisomerases; DNA topology; gene expression; promoter-proximal pausing; transcription elongation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line, Transformed
  • DNA Topoisomerases, Type II / genetics*
  • DNA Topoisomerases, Type II / metabolism
  • DNA, Superhelical / genetics*
  • DNA, Superhelical / metabolism
  • Epithelial Cells / cytology
  • Epithelial Cells / drug effects
  • Epithelial Cells / enzymology
  • Gene Expression Regulation
  • Genes, Immediate-Early
  • Humans
  • Poly-ADP-Ribose Binding Proteins / antagonists & inhibitors
  • Poly-ADP-Ribose Binding Proteins / genetics*
  • Poly-ADP-Ribose Binding Proteins / metabolism
  • Promoter Regions, Genetic
  • Protein Binding
  • Proto-Oncogene Proteins c-fos / genetics*
  • Proto-Oncogene Proteins c-fos / metabolism
  • RNA Polymerase II / genetics*
  • RNA Polymerase II / metabolism
  • Retinal Pigment Epithelium / cytology
  • Retinal Pigment Epithelium / drug effects
  • Retinal Pigment Epithelium / enzymology
  • Thiobarbiturates / pharmacology
  • Topoisomerase II Inhibitors / pharmacology
  • Transcription, Genetic*

Substances

  • DNA, Superhelical
  • Poly-ADP-Ribose Binding Proteins
  • Proto-Oncogene Proteins c-fos
  • Thiobarbiturates
  • Topoisomerase II Inhibitors
  • RNA Polymerase II
  • DNA Topoisomerases, Type II
  • TOP2A protein, human
  • merbarone