{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Jones RM"],"funding":["Lister Institute of Preventive Medicine","Wellcome Trust"],"pagination":["110260"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC11269944"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["27(7)"],"pubmed_abstract":["To ensure timely duplication of the entire eukaryotic genome, thousands of replication machineries (replisomes) act on genomic DNA at any time during S phase. In the final stages of this process, replisomes are unloaded from chromatin. Unloading is driven by polyubiquitylation of MCM7, a subunit of the terminated replicative helicase, and processed by p97/VCP segregase. Most of our knowledge of replication termination comes from model organisms, and little is known about how this process is executed and regulated in human somatic cells. Here we show that replisome disassembly in this system requires CUL2<sup>LRR1</sup>-driven MCM7 ubiquitylation, p97, and UBXN7 for unloading and provide evidence for \"backup\" mitotic replisome disassembly, demonstrating conservation of such mechanisms. Fina"],"journal":["iScience"],"pubmed_title":["Characterizing replisome disassembly in human cells."],"pmcid":["PMC11269944"],"funding_grant_id":["215510/Z/19/Z"],"pubmed_authors":["Natsume T","Romero F","Gambus A","Bristow RG","Jones RM","Henklewska M","Scaramuzza S","Liu C","Kanemaki MT","Nath S","Ruiz JH"],"additional_accession":[]},"is_claimable":false,"name":"Characterizing replisome disassembly in human cells.","description":"To ensure timely duplication of the entire eukaryotic genome, thousands of replication machineries (replisomes) act on genomic DNA at any time during S phase. In the final stages of this process, replisomes are unloaded from chromatin. Unloading is driven by polyubiquitylation of MCM7, a subunit of the terminated replicative helicase, and processed by p97/VCP segregase. Most of our knowledge of replication termination comes from model organisms, and little is known about how this process is executed and regulated in human somatic cells. Here we show that replisome disassembly in this system requires CUL2<sup>LRR1</sup>-driven MCM7 ubiquitylation, p97, and UBXN7 for unloading and provide evidence for \"backup\" mitotic replisome disassembly, demonstrating conservation of such mechanisms. Fina","dates":{"release":"2024-01-01T00:00:00Z","publication":"2024 Jul","modification":"2026-06-02T23:34:11.469Z","creation":"2025-04-19T13:11:42.977Z"},"accession":"S-EPMC11269944","cross_references":{"pubmed":["39055910"],"doi":["10.1016/j.isci.2024.110260"]}}