Competition for the nascent leading strand shapes the requirements for PCNA loading in the replisome
During DNA replication, the DNA polymerases Pol δ and Pol ε utilise the ring-shaped sliding clamp PCNA to enhance their processivity. PCNA loading onto DNA is accomplished by the clamp loaders RFC and Ctf18-RFC, which function primarily on the lagging and the leading strand, respectively. RFC activity is essential for lagging-strand replication by Pol δ, but it is unclear why Ctf18-RFC is required for leading-strand PCNA loading and why RFC cannot fulfil this function. Here, we show that RFC cannot load PCNA once Pol ε has been incorporated into the budding yeast replisome and commenced leading-strand synthesis, and this state is maintained during replisome progression. By contrast, we find that Ctf18-RFC is uniquely equipped to load PCNA onto the leading strand and show that this activity requires a direct interaction between Ctf18 and the CMG (Cdc45-MCM-GINS) helicase. Our work uncovers a mechanistic basis for why replisomes require a dedicated leading-strand clamp loader.
Authors
- Emma E Fletcher (ORCID: https://orcid.org/0000-0002-0792-5212)
- Morgan Jones (ORCID: https://orcid.org/0000-0003-1948-4925)
- Joseph T.P. Yeeles (ORCID: https://orcid.org/0000-0002-2255-2119)
Institutions
- MRC Laboratory of Molecular Biology (GB)
Publication Details
- Journal
- The EMBO Journal
- Published
- 2025-02-28
- DOI
- https://doi.org/10.1038/s44318-025-00386-4
- Citations
- 6
- Primary Topic
- DNA Repair Mechanisms
- Type
- article
- Field-Weighted Citation Impact
- 4.84
Funders
- Medical Research Council