Abstract
FAN1 is a DNA dependent nuclease whose proper function is essential for maintaining human health. For example, a genetic variant in FAN1, Arg507 to His hastens onset of Huntington’s disease, a repeat expansion disorder for which there is no cure. How the Arg507His mutation affects FAN1 structure and enzymatic function is unknown. Using cryo-EM and biochemistry, we have discovered that FAN1 arginine 507 is critical for its interaction with PCNA, and mutation of Arg507 to His attenuates assembly of the FAN1–PCNA complex on a disease-relevant extrahelical DNA extrusions formed within DNA repeats. This mutation concomitantly abolishes PCNA–FAN1–dependent cleavage of such extrusions, thus unraveling the molecular basis for a specific mutation in FAN1 that dramatically hastens the onset of Huntington’s disease. These results underscore the importance of PCNA to the genome stabilizing function of FAN1.
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CITATION STYLE
Li, F., Phadte, A. S., Bhatia, M., Barndt, S., Monte Carlo, A. R., Hou, C. F. D., … Pluciennik, A. (2025). Structural and molecular basis of PCNA-activated FAN1 nuclease function in DNA repair. Nature Communications , 16(1). https://doi.org/10.1038/s41467-025-59323-y
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