The function of human PIF1 in G quadruplex formation and replication stress response at ALT telomeres

Ragupathi, A., Zhao, R., Najit, S., Fernandez, A., Abid, H. Z., Mo, J., Juang, S., Tong, C., Yetil, D., Buchanan, L., et al.

10.64898/2026.08.31.748286 · was preprinted

discovery

Surfaced because: matches the platform's topic region.

relevance 0.29 openness 0.00 novelty 0.27

Abstract

Cancers maintain their telomeres through two telomere maintenance mechanisms: 85-90% of cancers rely on telomerase (TEL+), while 10-15% of cancers adopt the Alternative Lengthening of Telomeres (ALT) pathway. The Break-Induced Replication (BIR) pathway plays a critical role in maintaining telomere length in the ALT+ cells. In both yeast and human, PIF1, a 5' to 3' helicase, is required for the robust activity of BIR. However, the extent of human PIF1 (hPIF1) involvement in the ALT pathway remains unknown. Here we showed that hPIF1 can be recruited to damaged telomeres in ALT+ cells. In addition, we demonstrated that inhibition of hPIF1 induced DNA damage and G quadruplex (G4) accumulation at ALT telomeres, leading to a moderate reduction of the mean telomere length. Most interestingly, we demonstrated that inhibition of hPIF1 also attenuates checkpoint activation, BLM recruitment, single-stranded DNA (ssDNA) formation, DNA damage, and G4s at telomeres in the FANCM deficient ALT+ cells. Finally, we showed that inactivation of hPIF1 affects the viability of both ALT+ and TEL+ cancers, suggesting that hPIF1 is a potential drug target for cancer therapy.

Lifecycle

biorxiv v1 2026-09-01 source ↗

Discussion

No qualifying discussion yet.