Mechanisms of eukaryotic replisome disassembly

• Published in: Biochemical Society transactions Vol. 48; no. 3; p. 823
• Main Authors: Moreno, Sara Priego, Gambus, Agnieszka
• Format: Journal Article
• Language: English
• Published: England 30-06-2020
• Subjects: Animals; Caenorhabditis elegans; Cell Cycle; Cell Cycle Proteins - metabolism; Cell Survival; DNA - metabolism; DNA Replication; Genome; Humans; Minichromosome Maintenance Complex Component 7 - metabolism; Mitosis; Neoplasms - metabolism; Protein Interaction Mapping; Replication Origin; S Phase; Saccharomyces cerevisiae; Saccharomycetales - metabolism; Ubiquitin - metabolism; Ubiquitin-Protein Ligases - metabolism; Ubiquitination; Xenopus laevis; Cullin2-LRR1; replisome disassembly; genome integrity; ubiquitylation; TRAIP; p97
• ISSN: 1470-8752
• DOI: 10.1042/bst20190363

DNA replication is a complex process that needs to be executed accurately before cell division in order to maintain genome integrity. DNA replication is divided into three main stages: initiation, elongation and termination. One of the key events during initiation is the assembly of the replicative helicase at origins of replication, and this mechanism has been very well described over the last decades. In the last six years however, researchers have also focused on deciphering the molecular mechanisms underlying the disassembly of the replicative helicase during termination. Similar to replisome assembly, the mechanism of replisome disassembly is strictly regulated and well conserved throughout evolution, although its complexity increases in higher eukaryotes. While budding yeast rely on just one pathway for replisome disassembly in S phase, higher eukaryotes evolved an additional mitotic pathway over and above the default S phase specific pathway. Moreover, replisome disassembly has been recently found to be a key event prior to the repair of certain DNA lesions, such as under-replicated DNA in mitosis and inter-strand cross-links (ICLs) in S phase. Although replisome disassembly in human cells has not been characterised yet, they possess all of the factors involved in these pathways in model organisms, and de-regulation of many of them are known to contribute to tumorigenesis and other pathological conditions.