Abstract

In eukaryotes, the perfect duplication of the chromosomes is executed by a dynamic molecular machine called the replisome. As a key step to finishing DNA replication, replisome disassembly is triggered by ubiquitylation of the MCM7 subunit of the helicase complex CMG. Afterwards, the CDC48/p97 “unfoldase” is recruited to the ubiquitylated helicase to unfold MCM7 and disassemble the replisome. Here we summarise recently discovered mechanisms of replisome disassembly that are likely to be broadly conserved in eukaryotes. We also discuss two crucial questions that remain to be explored further in the future. Firstly, how is CMG ubiquitylation repressed by the replication fork throughout elongation? Secondly, what is the biological significance of replisome disassembly and what are the consequences of failing to ubiquitylate and disassemble the CMG helicase?

Highlights

  • Frontiers in Cell and Developmental BiologyThe perfect duplication of the chromosomes is executed by a dynamic molecular machine called the replisome

  • The MRC Protein Phosphorylation and Ubiquitylation Unit, School of Life Sciences, University of Dundee, Dundee, United Kingdom

  • How is CMG ubiquitylation repressed by the replication fork throughout elongation? Secondly, what is the biological significance of replisome disassembly and what are the consequences of failing to ubiquitylate and disassemble the CMG helicase?

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Summary

Frontiers in Cell and Developmental Biology

The perfect duplication of the chromosomes is executed by a dynamic molecular machine called the replisome. As a key step to finishing DNA replication, replisome disassembly is triggered by ubiquitylation of the MCM7 subunit of the helicase complex CMG. Afterwards, the CDC48/p97 “unfoldase” is recruited to the ubiquitylated helicase to unfold MCM7 and disassemble the replisome. We summarise recently discovered mechanisms of replisome disassembly that are likely to be broadly conserved in eukaryotes. We discuss two crucial questions that remain to be explored further in the future. How is CMG ubiquitylation repressed by the replication fork throughout elongation? What is the biological significance of replisome disassembly and what are the consequences of failing to ubiquitylate and disassemble the CMG helicase?

OVERVIEW OF DNA REPLICATION TERMINATION
FORK CONVERGENCE
CMG DISASSEMBLY IN BUDDING YEAST
CMG DISASSEMBLY IN METAZOA
Full Text
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