Structural basis of gap-filling DNA synthesis in the nucleosome by DNA Polymerase β

Nat Commun. 2025 Mar 17;16(1):2607. doi: 10.1038/s41467-025-57915-2.

Abstract

Single-strand breaks (SSBs) are one of the most prevalent forms of DNA damage found in the chromatinized genome and are repaired by single-strand break repair (SSBR) or base excision repair (BER). DNA polymerase beta (Pol β) is the primary enzyme responsible for processing the 1-nt gap intermediate in chromatin during SSBR and BER. To date, the mechanism used by Pol β to process a 1-nt gap in the context of chromatin remains poorly understood. Here, we use biochemical assays and cryogenic electron microscopy (cryo-EM) to determine the kinetic and structural basis of gap-filling DNA synthesis in the nucleosome by Pol β. This work establishes that Pol β uses a global DNA sculpting mechanism for processing 1-nt gaps in the nucleosome during SSBR and BER, providing fundamental insight into DNA repair in chromatin.

MeSH terms

  • Chromatin / metabolism
  • Cryoelectron Microscopy
  • DNA Breaks, Single-Stranded
  • DNA Polymerase beta* / chemistry
  • DNA Polymerase beta* / genetics
  • DNA Polymerase beta* / metabolism
  • DNA Repair
  • DNA Replication*
  • DNA* / biosynthesis
  • DNA* / chemistry
  • DNA* / metabolism
  • Humans
  • Kinetics
  • Nucleosomes* / genetics
  • Nucleosomes* / metabolism
  • Nucleosomes* / ultrastructure

Substances

  • DNA Polymerase beta
  • Nucleosomes
  • DNA
  • Chromatin