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TitleA mechanistic model of primer synthesis from catalytic structures of DNA polymerase α-primase.
Journal, issue, pagesbioRxiv, Year 2023
Publish dateSep 28, 2023
AuthorsElwood A Mullins / Lauren E Salay / Clarissa L Durie / Noah P Bradley / Jane E Jackman / Melanie D Ohi / Walter J Chazin / Brandt F Eichman
PubMed AbstractThe mechanism by which polymerase α-primase (polα-primase) synthesizes chimeric RNA-DNA primers of defined length and composition, necessary for replication fidelity and genome stability, is ...The mechanism by which polymerase α-primase (polα-primase) synthesizes chimeric RNA-DNA primers of defined length and composition, necessary for replication fidelity and genome stability, is unknown. Here, we report cryo-EM structures of polα-primase in complex with primed templates representing various stages of DNA synthesis. Our data show how interaction of the primase regulatory subunit with the primer 5'-end facilitates handoff of the primer to polα and increases polα processivity, thereby regulating both RNA and DNA composition. The structures detail how flexibility within the heterotetramer enables synthesis across two active sites and provide evidence that termination of DNA synthesis is facilitated by reduction of polα and primase affinities for the varied conformations along the chimeric primer/template duplex. Together, these findings elucidate a critical catalytic step in replication initiation and provide a comprehensive model for primer synthesis by polα-primase.
External linksbioRxiv / PubMed:36993335 / PubMed Central
MethodsEM (single particle)
Resolution3.9 Å
Structure data

EMDB-29886: Partial DNA termination subcomplex of Xenopus laevis DNA polymerase alpha-primase
Method: EM (single particle) / Resolution: 3.9 Å

Source
  • Xenopus laevis (African clawed frog)
  • synthetic construct (others)

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