4.8 Article

Concerted Loading of Mcm2-7 Double Hexamers around DNA during DNA Replication Origin Licensing

Journal

CELL
Volume 139, Issue 4, Pages 719-730

Publisher

CELL PRESS
DOI: 10.1016/j.cell.2009.10.015

Keywords

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Funding

  1. Cancer Research UK
  2. Institute of Cancer Research
  3. National Institutes of Health [GM31819, ES13773]
  4. European Molecular Biology Organization long-term fellowship

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The licensing of eukaryotic DNA replication origins, which ensures once-per-cell-cycle replication, involves the loading of six related minichromosome maintenance proteins (Mcm2-7) into prereplicative complexes (pre-RCs). Mcm2-7 forms the core of the replicative DNA helicase, which is inactive in the pre-RC. The loading of Mcm2-7 onto DNA requires the origin recognition complex (ORC), Cdc6, and Cdt1, and depends on ATP. We have reconstituted Mcm2-7 loading with purified budding yeast proteins. Using biochemical approaches and electron microscopy, we show that single heptamers of Cdt1 center dot Mcm2-7 are loaded cooperatively and result in association of stable, head-to-head Mcm2-7 double hexamers connected via their N-terminal rings. DNA runs through a central channel in the double hexamer, and, once loaded, Mcm2-7 can slide passively along double-stranded DNA. Our work has significant implications for understanding how eukaryotic DNA replication origins are chosen and licensed, how replisomes assemble during initiation, and how unwinding occurs during DNA replication.

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