Journal article

Cyclin-dependent kinase-mediated phosphorylation of FANCD2 promotes mitotic fidelity

JA Cantres-Velez, JL Blaize, DA Vierra, RA Boisvert, JL Garzon, B Piraino, W Tan, AJ Deans, NG Howlett

Molecular and Cellular Biology | Published : 2021

Abstract

Fanconi anemia (FA) is a rare genetic disease characterized by increased risk for bone marrow failure and cancer. The FA proteins function together to repair damaged DNA. A central step in the activation of the FA pathway is the monoubiquitination of the FANCD2 and FANCI proteins, which occurs upon exposure to DNA-damaging agents and during the S phase of the cell cycle. The regulatory mechanisms governing S-phase monoubiquitination, in particular, are poorly understood. In this study, we have identified a cyclin-dependent kinase (CDK) regulatory phosphosite (S592) proximal to the site of FANCD2 monoubiquitination. FANCD2 S592 phosphorylation was detected by liquid chromatography-tandem mass..

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University of Melbourne Researchers

Grants

Awarded by National Institutes of Health


Funding Acknowledgements

This work was supported by NIH/NHLBI grant R01HL149907 (to N.G.H.), an American Society of Hematology Bridge grant (to N.G.H.), Rhode Island IDeA Network of Biomedical Research Excellence (RI-INBRE) grant P20GM103430 from the National Institute of General Medical Science, and Rhode Island Experimental Program to Stimulate Competitive Research (RI-EPSCoR) grant no. 1004057 from the National Science Foundation.