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Ufd1-Npl4 Recruit Cdc48 for Disassembly of Ubiquitylated CMG Helicase at the End of Chromosome Replication

Overview
Journal Cell Rep
Publisher Cell Press
Date 2017 Mar 30
PMID 28355556
Citations 26
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Abstract

Disassembly of the Cdc45-MCM-GINS (CMG) DNA helicase is the key regulated step during DNA replication termination in eukaryotes, involving ubiquitylation of the Mcm7 helicase subunit, leading to a disassembly process that requires the Cdc48 "segregase". Here, we employ a screen to identify partners of budding yeast Cdc48 that are important for disassembly of ubiquitylated CMG helicase at the end of chromosome replication. We demonstrate that the ubiquitin-binding Ufd1-Npl4 complex recruits Cdc48 to ubiquitylated CMG. Ubiquitylation of CMG in yeast cell extracts is dependent upon lysine 29 of Mcm7, which is the only detectable site of ubiquitylation both in vitro and in vivo (though in vivo other sites can be modified when K29 is mutated). Mutation of K29 abrogates in vitro recruitment of Ufd1-Npl4-Cdc48 to the CMG helicase, supporting a model whereby Ufd1-Npl4 recruits Cdc48 to ubiquitylated CMG at the end of chromosome replication, thereby driving the disassembly reaction.

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References
1.
Davis E, Lachaud C, Appleton P, Macartney T, Nathke I, Rouse J . DVC1 (C1orf124) recruits the p97 protein segregase to sites of DNA damage. Nat Struct Mol Biol. 2012; 19(11):1093-100. DOI: 10.1038/nsmb.2394. View

2.
Verma R, Oania R, Fang R, Smith G, Deshaies R . Cdc48/p97 mediates UV-dependent turnover of RNA Pol II. Mol Cell. 2011; 41(1):82-92. PMC: 3063307. DOI: 10.1016/j.molcel.2010.12.017. View

3.
Moyer S, Lewis P, Botchan M . Isolation of the Cdc45/Mcm2-7/GINS (CMG) complex, a candidate for the eukaryotic DNA replication fork helicase. Proc Natl Acad Sci U S A. 2006; 103(27):10236-10241. PMC: 1482467. DOI: 10.1073/pnas.0602400103. View

4.
Li N, Zhai Y, Zhang Y, Li W, Yang M, Lei J . Structure of the eukaryotic MCM complex at 3.8 Å. Nature. 2015; 524(7564):186-91. DOI: 10.1038/nature14685. View

5.
Shevchenko A, Tomas H, Havlis J, Olsen J, Mann M . In-gel digestion for mass spectrometric characterization of proteins and proteomes. Nat Protoc. 2007; 1(6):2856-60. DOI: 10.1038/nprot.2006.468. View