DNA translocation mechanism of the MCM complex and implications for replication initiation
Open Access
- 15 July 2019
- journal article
- research article
- Published by Springer Nature in Nature Communications
- Vol. 10 (1) , 1-13
Abstract
The DNA translocation activity of the minichromosome maintenance (MCM) complex powers DNA strand separation of the replication forks of eukaryotes and archaea. Here we illustrate an atomic level mechanism for this activity with a crystal structure of an archaeal MCM hexamer bound to single-stranded DNA and nucleotide cofactors. Sequence conservation indicates this rotary mechanism is fully possible for all eukaryotes and archaea. The structure definitively demonstrates the ring orients during translocation with the N-terminal domain leading, indicating that the translocation activity could also provide the physical basis of replication initiation where a double-hexamer idly encircling double-stranded DNA transforms to single-hexamers that encircle only one strand. In this mechanism, each strand binds to the N-terminal tier of one hexamer and the AAA+ tier of the other hexamer such that one ring pulls on the other, aligning equivalent interfaces to enable each hexamer to pull its translocation strand outside of the opposing hexamer.Keywords
Funding Information
- U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (R01GM098771)
- American Lebanese Syrian Associated Charities
This publication has 65 references indexed in Scilit:
- Bypass of a protein barrier by a replicative DNA helicaseNature, 2012
- Selective Bypass of a Lagging Strand Roadblock by the Eukaryotic Replicative DNA HelicaseCell, 2011
- Uncoupling of Sister Replisomes during Eukaryotic DNA ReplicationMolecular Cell, 2010
- Concerted Loading of Mcm2–7 Double Hexamers around DNA during DNA Replication Origin LicensingCell, 2009
- Running in Reverse: The Structural Basis for Translocation Polarity in Hexameric HelicasesCell, 2009
- The Mcm2-7 Complex Has In Vitro Helicase ActivityMolecular Cell, 2008
- Version 1.2 of the Crystallography and NMR systemNature Protocols, 2007
- Sequential ATP Hydrolysis by Cdc6 and ORC Directs Loading of the Mcm2-7 HelicaseMolecular Cell, 2006
- The structure and function of MCM from archaeal M. ThermoautotrophicumNature Structural & Molecular Biology, 2003
- ATP-dependent recognition of eukaryotic origins of DNA replication by a multiprotein complexNature, 1992