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Mechanism of PCNA loading by Ctf18-RFC for leading-strand DNA synthesis.
Yuan, Zuanning; Georgescu, Roxana; Yao, Nina Y; Yurieva, Olga; O'Donnell, Michael E; Li, Huilin.
Affiliation
  • Yuan Z; Department of Structural Biology, Van Andel Institute, Grand Rapids, MI, USA.
  • Georgescu R; DNA Replication Laboratory, The Rockefeller University, New York, NY, USA.
  • Yao NY; Howard Hughes Medical Institute, New York, NY, USA.
  • Yurieva O; DNA Replication Laboratory, The Rockefeller University, New York, NY, USA.
  • O'Donnell ME; DNA Replication Laboratory, The Rockefeller University, New York, NY, USA.
  • Li H; Howard Hughes Medical Institute, New York, NY, USA.
Science ; 385(6708): eadk5901, 2024 Aug 02.
Article in En | MEDLINE | ID: mdl-39088616
ABSTRACT
The proliferating cell nuclear antigen (PCNA) clamp encircles DNA to hold DNA polymerases (Pols) to DNA for processivity. The Ctf18-RFC PCNA loader, a replication factor C (RFC) variant, is specific to the leading-strand Pol (Polε). We reveal here the underlying mechanism of Ctf18-RFC specificity to Polε using cryo-electron microscopy and biochemical studies. We found that both Ctf18-RFC and Polε contain specific structural features that direct PCNA loading onto DNA. Unlike other clamp loaders, Ctf18-RFC has a disordered ATPase associated with a diverse cellular activities (AAA+) motor that requires Polε to bind and stabilize it for efficient PCNA loading. In addition, Ctf18-RFC can pry prebound Polε off of DNA, then load PCNA onto DNA and transfer the PCNA-DNA back to Polε. These elements in both Ctf18-RFC and Polε provide specificity in loading PCNA onto DNA for Polε.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Proliferating Cell Nuclear Antigen / DNA Replication / Replication Protein C Limits: Humans Language: En Journal: Science Year: 2024 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Proliferating Cell Nuclear Antigen / DNA Replication / Replication Protein C Limits: Humans Language: En Journal: Science Year: 2024 Document type: Article Affiliation country: United States