J

John F.X. Diffley

The Francis Crick Institute

ORCID: 0000-0001-5184-7680

Publishes on DNA Repair Mechanisms, Genomics and Chromatin Dynamics, Fungal and yeast genetics research. 195 papers and 20.5k citations.

195Publications
20.5kTotal Citations

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Top publicationsby citations

Uninterrupted MCM2-7 Function Required for DNA Replication Fork Progression
Cited by 625

Little is known about the DNA helicases required for the elongation phase of eukaryotic chromosome replication. Minichromosome maintenance (MCM) protein complexes have DNA helicase activity but have only been functionally implicated in initiating DNA replication. Using an improved method for constructing conditional degron mutants, we show that depletion of MCMs after initiation irreversibly blocks the progression of replication forks in Saccharomyces cerevisiae. Like the Escherichia coli dnaB and SV40 T antigen helicases, therefore, the MCM complex is loaded at origins before initiation and is essential for elongation. Restricting MCM loading to the G(1) phase ensures that initiation and elongation occur just once per cell cycle.