Structural basis of gap-filling DNA synthesis in the nucleosome by DNA Polymerase β
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.
Authors
- Jonah J. Spencer
- Spencer H. Thompson (ORCID: https://orcid.org/0009-0007-2122-546X)
- Adil S. Hussen
- Bret Freudenthal (ORCID: https://orcid.org/0000-0003-1449-4710)
- Tyler Weaver (ORCID: https://orcid.org/0000-0002-5138-7140)
- Nicholas Schnicker (ORCID: https://orcid.org/0000-0002-5189-4943)
- Benjamin Ryan (ORCID: https://orcid.org/0000-0001-8262-8659)
- Zhen Xu (ORCID: https://orcid.org/0000-0001-8855-0565)
Institutions
- University of Iowa (US)
- The University of Kansas Cancer Center (US)
- University of Kansas Medical Center (US)
Publication Details
- Journal
- Nature Communications
- Published
- 2025-03-17
- DOI
- https://doi.org/10.1038/s41467-025-57915-2
- Citations
- 4
- Primary Topic
- DNA Repair Mechanisms
- Type
- article
- Field-Weighted Citation Impact
- 3.22
Funders
- National Institute of General Medical Sciences