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.

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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

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article

Competition for the nascent leading strand shapes the requirements for PCNA loading in the replisome

Emma E Fletcher, Morgan Jones, Joseph T.P. Yeeles
6 citations
The EMBO Journal
DNA Repair Mechanisms
4.84
article

Competition for the nascent leading strand shapes the requirements for PCNA loading in the replisome

Emma E Fletcher, Morgan Jones, Joseph T.P. Yeeles
article en
6 citations

Abstract

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.

The EMBO JournalVol. 44(8)
MRC Laboratory of Molecular Biology (GB)
Medical Research Council
Openalex Percentile: Top 5%
DNA Repair Mechanisms
4.84
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Competition for the nascent leading strand shapes the requirements for PCNA loading in the replisome — Emma E Fletcher, Morgan Jones, et al. · The EMBO Journal (2025) | TGRS Research Map | TGRS