The PIN1-p38-CtIP signaling axis protects stalled replication forks from deleterious degradation
Human CtIP plays a critical role in homologous recombination (HR) by promoting the resection of DNA double-strand breaks. Moreover, CtIP maintains genome stability through protecting stalled replication forks from nucleolytic degradation. However, the upstream signaling mechanisms governing the mole...
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| Veröffentlicht in: | bioRxiv |
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| Hauptverfasser: | , , , , , , , , , , , , , , , , , , |
| Format: | Paper |
| Sprache: | Englisch |
| Veröffentlicht: |
Cold Spring Harbor Laboratory
26.06.2024
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| Ausgabe: | 1.1 |
| Schlagworte: | |
| ISSN: | 2692-8205 |
| Online-Zugang: | Volltext |
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| Zusammenfassung: | Human CtIP plays a critical role in homologous recombination (HR) by promoting the resection of DNA double-strand breaks. Moreover, CtIP maintains genome stability through protecting stalled replication forks from nucleolytic degradation. However, the upstream signaling mechanisms governing the molecular switch between these two CtIP-dependent processes remain largely elusive. Here, we show that phosphorylation of CtIP by the p38α stress kinase and subsequent PIN1-mediated CtIP cis-to-trans isomerization is required for fork stabilization but dispensable for HR. We found that stalled forks are degraded in cells expressing non-phosphorylatable CtIP or lacking PIN1-p38α activity, while expression of a CtIP trans-locked mutant overcomes the requirement for PIN1-p38α in fork protection. We further reveal that Brca1-deficient mammary tumor cells that have acquired PARPi resistance regain chemosensitivity after PIN1 or p38α inhibition. Collectively, our findings identify the PIN1-p38-CtIP signaling pathway as a critical regulator of replication fork integrity. |
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| ISSN: | 2692-8205 |
| DOI: | 10.1101/2024.06.25.600562 |