Structural basis for continuous DNA-end protection during ligation of double-strand breaks in yeast Non-Homologous End-Joining
Authors:
- Sophia MissourySMSophia Missoury
- Claire TettaravouCTClaire Tettaravou
- Sara CastelliSCSara Castelli
- Paloma Fernández VarelaPVPaloma Fernández Varela
- Virginie RoparsVRVirginie Ropars
- Stefano MattarocciSMStefano Mattarocci
- Pierre LegrandPLPierre Legrand
- Mauro ModestiMMMauro Modesti
- Stéphane MarcandSMStéphane Marcand
- Jean-Baptiste CharbonnierJCJean-Baptiste Charbonnier
Preprint
Abstract
Non-homologous end joining (NHEJ) repairs DNA double-strand breaks by synapsing and ligating DNA ends. In vertebrates, DNA-PKcs promotes end alignment and processing, yet several eukaryotes - including budding yeast - perform NHEJ without DNA-PKcs, and the underlying mechanism remains unclear. Here we report cryo-electron microscopy structures of reconstituted Saccharomyces cerevisiae NHEJ synaptic complexes assembled on DNA ends bearing either 4-bp terminal microhomologies or blunt termini. On the microhomology substrate with a single 5’-P, we capture a ligation-competent short-range complex in which a single Dnl4 catalytic core is fully ordered and engaged at the 5′-adenylated nick. When two 5’-P are present, we resolve two predominant, coexisting DNA-aligned protective states in which both Dnl4 DBD-NTD modules occupy the break region with reciprocal geometries, supporting an alternating engagement model for sequential sealing of the two strands while maintaining continuous end association. In contrast, blunt-ended substrates yield a non-aligned protective configuration in which two Dnl4 catalytic modules constrain the DNA ends ∼30 Å apart in a ligation-incompatible arrangement, providing a structural explanation for slow blunt-end joining in yeast. Together, these structures define architectural and mechanistic principles of DNA-PKcs-independent NHEJ.Keywords
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