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bioRxiv · 10.1101/2024.11.01.621514

The mechanism of checkpoint-dependent DNA replication fork stabilization in human cells

Bertolin, A. P.·Canal, B.·Yekezare, M.·Zeng, J.·Instrell, R.·Howell, M.·Diffley, J. F. X.
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Abstract

The DNA damage checkpoint is crucial for maintaining genome stability after genotoxic stress; without it, excess DNA replication origins are activated, stalled DNA replication forks cannot restart normally, high levels of DNA damage and single-stranded DNA (ssDNA) accumulate and cells cannot complete S phase. Preventing excess origin firing suppresses all these effects. Here we show that when replication is not restrained by a functional checkpoint, excess DNA synthesis sequesters the processivity factor PCNA and its loader RFC, preventing normal fork restart. Nascent DNA ends unprotected by RFC/PCNA are attacked by the Helicase-Like Transcription Factor (HLTF), causing irreversible replication fork collapse and hyperaccumulation of single-stranded DNA. This explains how the checkpoint stabilizes stalled replication forks and has implications for how origin firing is normally coordinated with fork progression. Loss of HLTF suppresses fork collapse and cell lethality in checkpoint-deficient cells, which has implications for how resistance to anti-checkpoint therapies may arise.

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Bertolin, A. P., Canal, B., Yekezare, M., Zeng, J., Instrell, R., Howell, M., Diffley, J. F. X.. 2024-11-03. The mechanism of checkpoint-dependent DNA replication fork stabilization in human cells. https://doi.org/10.1101/2024.11.01.621514

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