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Journal Article

CRL2(Lrr1) promotes unloading of the vertebrate replisome from chromatin during replication termination

MPS-Authors
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Mann,  Matthias
Mann, Matthias / Proteomics and Signal Transduction, Max Planck Institute of Biochemistry, Max Planck Society;

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Räschle,  Markus
Mann, Matthias / Proteomics and Signal Transduction, Max Planck Institute of Biochemistry, Max Planck Society;

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http://genesdev.cshlp.org/content/31/3/275/suppl/DC1
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Genes Dev.-2017-Dewar-275-90.pdf
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Citation

Dewar, J. M., Low, E., Mann, M., Räschle, M., & Walter, J. C. (2017). CRL2(Lrr1) promotes unloading of the vertebrate replisome from chromatin during replication termination. Genes and Development, 31(3), 275-290. doi:10.1101/gad.291799.116.


Cite as: https://hdl.handle.net/21.11116/0000-0001-6EA9-6
Abstract
A key event during eukaryotic replication termination is the removal of the CMG helicase from chromatin. CMG unloading involves ubiquitylation of its Mcm7 subunit and the action of the p97 ATPase. Using a proteomic screen in Xenopus egg extracts, we identified factors that are enriched on chromatin whenCMGunloading is blocked. This approach identified the E3 ubiquitin ligase CRL2(Lrr1), a specific p97 complex, other potential regulators of termination, and many replisome components. We show that Mcm7 ubiquitylation and CRL2(Lrr1) binding to chromatin are temporally linked and occur only during replication termination. In the absence of CRL2(Lrr1), Mcm7 is not ubiquitylated, CMG unloading is inhibited, and a large subcomplex of the vertebrate replisome that includes DNA Pol epsilon is retained on DNA. Our data identify CRL2(Lrr1) as a master regulator of replisome disassembly during vertebrate DNA replication termination.