Concerted Loading of Mcm2–7 Double Hexamers around DNA during DNA Replication Origin Licensing
Author(s) -
Dirk Remus,
Fabienne Beuron,
Gökhan Tolun,
Jack D. Griffith,
Edward P. Morris,
John F.X. Diffley
Publication year - 2009
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2009.10.015
Subject(s) - minichromosome maintenance , origin recognition complex , biology , control of chromosome duplication , replisome , pre replication complex , eukaryotic dna replication , dna replication factor cdt1 , dna replication , origin of replication , microbiology and biotechnology , replication factor c , dna , biophysics , genetics
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*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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