NYMC Faculty Publications
DNA Polymerase Delta Interacting Protein 3 Facilitates the Activation and Maintenance of DNA Damage Checkpoint in Response to Replication Stress
Author Type(s)
Faculty
DOI
10.1002/ame2.12274
Journal Title
Animal Models and Experimental Medicine
First Page
461
Last Page
469
Document Type
Article
Publication Date
10-1-2022
Department
Biochemistry and Molecular Biology
Abstract
BACKGROUND: Replication stress response is crucial for the maintenance of a stable genome. POLDIP3 (DNA polymerase delta interacting protein 3) was initially identified as one of the DNA polymerase δ (Pol δ) interacting proteins almost 20 years ago. Using a variety of in vitro biochemical assays, we previously established that POLDIP3 is a key regulator of the enzymatic activity of Pol δ. However, the in vivo function of POLDIP3 in DNA replication and DNA damage response has been elusive. METHODS: We first generated POLDIP3 knockout (KO) cells using the CRISPR/Cas9 technology. We then investigated its biological functions in vivo using a variety of biochemical and cell biology assays. RESULTS: We showed that although the POLDIP3-KO cells manifest no pronounced defect in global DNA synthesis under nonstress conditions, they are sensitive to a variety of replication fork blockers. Intriguingly, we found that POLDIP3 plays a crucial role in the activation and maintenance of the DNA damage checkpoint in response to exogenous as well as endogenous replication stress. CONCLUSION: Our results indicate that when the DNA replication fork is blocked, POLDIP3 can be recruited to the stalled replication fork and functions to bridge the early DNA damage checkpoint response and the later replication fork repair/restart.
Recommended Citation
Zhang, S., Lee, E. Y., Lee, M. Y., & Zhang, D. (2022). DNA Polymerase Delta Interacting Protein 3 Facilitates the Activation and Maintenance of DNA Damage Checkpoint in Response to Replication Stress. Animal Models and Experimental Medicine, 5 (5), 461-469. https://doi.org/10.1002/ame2.12274
