Transcription-Replication Collisions-A Series of Unfortunate Events

Biomolecules. 2021 Aug 21;11(8):1249. doi: 10.3390/biom11081249.

Abstract

Transcription-replication interactions occur when DNA replication encounters genomic regions undergoing transcription. Both replication and transcription are essential for life and use the same DNA template making conflicts unavoidable. R-loops, DNA supercoiling, DNA secondary structure, and chromatin-binding proteins are all potential obstacles for processive replication or transcription and pose an even more potent threat to genome integrity when these processes co-occur. It is critical to maintaining high fidelity and processivity of transcription and replication while navigating through a complex chromatin environment, highlighting the importance of defining cellular pathways regulating transcription-replication interaction formation, evasion, and resolution. Here we discuss how transcription influences replication fork stability, and the safeguards that have evolved to navigate transcription-replication interactions and maintain genome integrity in mammalian cells.

Keywords: DNA replication; R-loops; replication stress; transcription.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Animals
  • Chromatin / metabolism*
  • Chromosomes / metabolism
  • DNA / chemistry
  • DNA Damage
  • DNA Replication*
  • DNA Topoisomerases, Type II / chemistry
  • DNA-Binding Proteins / metabolism
  • DNA-Directed DNA Polymerase / chemistry
  • DNA-Directed RNA Polymerases / chemistry
  • Escherichia coli
  • Genomic Instability
  • Humans
  • Mice
  • Nucleic Acid Conformation
  • Nucleotides / chemistry
  • Oncogenes
  • Protein Binding
  • Reproducibility of Results
  • Ribonuclease H / chemistry
  • Saccharomyces cerevisiae
  • Stochastic Processes
  • Transcription, Genetic*

Substances

  • Chromatin
  • DNA-Binding Proteins
  • Nucleotides
  • DNA
  • DNA-Directed RNA Polymerases
  • DNA-Directed DNA Polymerase
  • Ribonuclease H
  • DNA Topoisomerases, Type II