Dbf4-Dependent Kinase Finetunes INO80 Function at Chromosome Replication Origins

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Dbf4-Dependent Kinase Finetunes INO80 Function at Chromosome Replication Origins

Authors

Kurat, C.; Bansal, P.; Lahiri, S.; Kumar, C.; Galanti, L.; Chacin, E.; Ortiz-Bazan, M. A.; Mueller, M.; Vizjak, P.; Straub, T.; Mueller-Planitz, F.; Aguilera, A.; Gomez-Gonzalez, B.; Pfander, B.; Imhof, A.

Abstract

The highly conserved Dbf4-Dependent Kinase (DDK) plays a pivotal role in the nucleus during S phase, where it directly phosphorylates the replicative helicase, the minichromosome maintenance (MCM) complex. This leads to the initiation of chromosome replication. However, aside from the MCM complex, few other targets have been identified to date, leaving DDK an understudied kinase. Here, we describe a two-pronged mass spectrometry-based approach and define the nuclear DDK-dependent phosphoproteome, which consists of approximately 400 phosphorylation events. Within this network, we found that DDK directly phosphorylates the Arp8 subunit of the multi-subunit chromatin remodeler complex INO80. Arp8 phosphorylation stabilises INO80\'s intramolecular complex integrity, which finetunes its nucleosome spacing activity at replication origins. This adjustment of origin chromatin architecture stimulates replication and is important for the response to replication stress. Our results represent a significant advance in our understanding of the molecular mechanisms underlying the regulation of replication origins.

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