GSK3β guides chromosomal repair pathway selection to support BRCA1-independent PARP inhibitor sensitivity

Glycogen synthase kinase-3β (GSK3β) is an established regulator in the DNA double-strand break (DSB) repair pathway. Recent work by Allam et al. revealed a mechanism of DSB repair pathway choice through GSK3β-mediated, site-specific phosphorylation of the tumor suppressor p53 binding protein 1 (53BP1) at threonine 334 (T334). 53BP1 T334 phosphorylation prevented interaction between 53BP1 and its downstream functional partners, PTIP and RIF1, thereby inhibiting 53BP1-directed nonhomologous end joining (NHEJ). Additionally, 53BP1 T334 phosphorylation promoted recruitment of CtIP and RPA32 to DNA damage sites to facilitate homologous recombination (HR). In contrast with loss of 53BP1 function, a 53BP1 T334A phospho-deficient mutant accumulated aberrantly at DSBs, where it impaired end resection and suppressed HR activity. These surprising results suggest that GSK3β may select between NHEJ and HR DNA repair pathways. Additionally, these data support targeting the GSK3β/53BP1 axis to enhance PARP inhibitor efficacy in solid tumors, regardless of BRCA1 status.

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Journal
Journal of Clinical Investigation
Published
2025-11-16
DOI
https://doi.org/10.1172/jci197910
Primary Topic
DNA Repair Mechanisms
Type
article
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article

GSK3β guides chromosomal repair pathway selection to support BRCA1-independent PARP inhibitor sensitivity

David R. Gius, Justin Leung
Journal of Clinical Investigation
DNA Repair Mechanisms
article

GSK3β guides chromosomal repair pathway selection to support BRCA1-independent PARP inhibitor sensitivity

David R. Gius, Justin Leung
article en

Abstract

Glycogen synthase kinase-3β (GSK3β) is an established regulator in the DNA double-strand break (DSB) repair pathway. Recent work by Allam et al. revealed a mechanism of DSB repair pathway choice through GSK3β-mediated, site-specific phosphorylation of the tumor suppressor p53 binding protein 1 (53BP1) at threonine 334 (T334). 53BP1 T334 phosphorylation prevented interaction between 53BP1 and its downstream functional partners, PTIP and RIF1, thereby inhibiting 53BP1-directed nonhomologous end joining (NHEJ). Additionally, 53BP1 T334 phosphorylation promoted recruitment of CtIP and RPA32 to DNA damage sites to facilitate homologous recombination (HR). In contrast with loss of 53BP1 function, a 53BP1 T334A phospho-deficient mutant accumulated aberrantly at DSBs, where it impaired end resection and suppressed HR activity. These surprising results suggest that GSK3β may select between NHEJ and HR DNA repair pathways. Additionally, these data support targeting the GSK3β/53BP1 axis to enhance PARP inhibitor efficacy in solid tumors, regardless of BRCA1 status.

Journal of Clinical InvestigationVol. 135(22)
The University of Texas at San Antonio Health Science Center (US)
Openalex Percentile: Top 68%
DNA Repair Mechanisms
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GSK3β guides chromosomal repair pathway selection to support BRCA1-independent PARP inhibitor sensitivity — David R. Gius, Justin Leung · Journal of Clinical Investigation (2025) | TGRS Research Map | TGRS