Apurinic/apyrimidinic endodeoxyribonuclease 1 contributes to the repair of damaged intercalated-motif of telomeric sequences
Alessia BellinaiD, Matilde Clarissa MalfattiiD, Tobias Obermann, Kayla GroomsiD, Andreas Gjosaether, Zahraa Othman, Gilmar F. J. SalgadoiD, Daniela MarascoiD, Antonella VirgilioiD, Veronica EspositoiD, Giulia AntonialiiD, Catia MioiD, Matteo Pivetta, Magnar BjøråsiD, Barbara van LooniD, Gianluca TelliD
Abstract
Apurinic/apyrimidinic endodeoxyribonuclease 1 (APE1) is a key enzyme in the Base Excision Repair pathway, responsible for processing abasic (AP-) sites. Recent studies revealed that APE1 participates in repairing DNA secondary structures as G-quadruplexes (G4). Telomeres, stabilized by shelterin proteins, are rich in G4, where APE1 binds and repairs AP-sites to maintain their integrity. The complementary cytosine-rich strand forms another structure, the i-motif (iM), essential for telomere maintenance, though its repair mechanism remains unclear. Herein we investigate APE1 binding and processing capabilities toward native and damaged telomeric iM, bearing AP-sites in different positions. Using biochemical and biophysical assays, we found that APE1 binds the telomeric iM-sequence and that its cleavage efficiency depends on AP-site position within iM. Proximity Ligation Assay analysis, in HeLa and U2OS cells, highlighted a novel interaction between APE1 and PCBP1, a well-known iM-folding modulator. PCBP1 binds iM with higher affinity than APE1 and inhibits its cleavage activity on damaged iM. Immunofluorescence and Telomere Restriction Fragment analyses showed that depletion of APE1 or PCBP1 impairs their interaction with the shelterin components, affecting telomere length. These results connect APE1 canonical DNA repair activity with the maintenance of non-canonical DNA secondary structures in telomeres, through its interaction with PCBP1. GRAPHICAL ABSTRACT O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=80 SRC="FIGDIR/small/694817v1_ufig1.gif" ALT="Figure 1"> View larger version (27K): org.highwire.dtl.DTLVardef@1962c63org.highwire.dtl.DTLVardef@3c3f60org.highwire.dtl.DTLVardef@164d78borg.highwire.dtl.DTLVardef@1831aae_HPS_FORMAT_FIGEXP M_FIG C_FIG
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 0
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Structural basis for APE1 processing DNA damage in the nucleosome
T. M. Weaver, N. M. Hoitsma, … B. D. Freudenthal·bioRxiv·Mar 9, 2022
- APE1 active site residue Asn174 stabilizes the AP-site and is essential for catalysis
Kaitlin M. DeHart, Nicole M. Hoitsma, … Bret Freudenthal·Journal of Biological ChemistryPeer-reviewed·Sep 1, 2025
- A Dynamic Search Mechanism Enables APE1 to Identify AP-Sites in DNA
Kaitlin M. DeHart, Peyton N. Oden, … Bret Freudenthal·Nucleic Acids ResearchPeer-reviewed·May 13, 2026
- Binding of AP endonuclease-1 to G-quadruplex DNA depends on the N-terminal domain, Mg2+ and ionic strength
A. M. Fleming, S. A. Howpay Manage, C. J. Burrows·ACS Bio & Med Chem AuPeer-reviewed·Oct 29, 2021
- Visualizing the Coordination of APE1 and DNA Polymerase β During Base Excision Repair
M. Fairlamb, T. Washington, B. D. Freudenthal·bioRxiv·May 2, 2022
- APE1 Coordinates Its Disordered Region and Metal Cofactors to Drive Genome Surveillance
Donghun Lee, S S Kim, … Gwangrog Lee·Nucleic Acids ResearchPeer-reviewed·May 1, 2026