
pmid: 16387651
Loading of the Mcm2-7 DNA replicative helicase onto origin-proximal DNA is a critical and tightly regulated event during the initiation of eukaryotic DNA replication. The resulting protein-DNA assembly is called the prereplicative complex (pre-RC), and its formation requires the origin recognition complex (ORC), Cdc6, Cdt1, and ATP. ATP hydrolysis by ORC is required for multiple rounds of Mcm2-7 loading. Here, we investigate the role of ATP hydrolysis by Cdc6 during pre-RC assembly. We find that Cdc6 is an ORC- and origin DNA-dependent ATPase that functions at a step preceding ATP hydrolysis by ORC. Inhibiting Cdc6 ATP hydrolysis stabilizes Cdt1 on origin DNA and prevents Mcm2-7 loading. In contrast, the initial association of Mcm2-7 with the other pre-RC components does not require ATP hydrolysis by Cdc6. Importantly, these coordinated yet distinct functions of ORC and Cdc6 ensure the correct temporal and spatial regulation of pre-RC formation.
DNA Replication, Saccharomyces cerevisiae Proteins, Chromosomal Proteins, Non-Histone, Cell Cycle, Origin Recognition Complex, Nuclear Proteins, Affinity Labels, Cell Cycle Proteins, Cell Biology, Saccharomyces cerevisiae, Minichromosome Maintenance Complex Component 7, Models, Biological, DNA-Binding Proteins, Fungal Proteins, Adenosine Triphosphate, Molecular Biology
DNA Replication, Saccharomyces cerevisiae Proteins, Chromosomal Proteins, Non-Histone, Cell Cycle, Origin Recognition Complex, Nuclear Proteins, Affinity Labels, Cell Cycle Proteins, Cell Biology, Saccharomyces cerevisiae, Minichromosome Maintenance Complex Component 7, Models, Biological, DNA-Binding Proteins, Fungal Proteins, Adenosine Triphosphate, Molecular Biology
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