Completed Genetics & Molecular Biology Cells, Biochemistry & Physiology

Replisome unloading: mechanism and importance for cell biology

In plain English

AI plain-English summary

Every time a human cell divides, it must copy its entire genome—and the molecular machinery that does the copying must then be dismantled, or the cell risks genetic chaos. Despite six decades of research into DNA replication, scientists still do not understand how this dismantling process works in human cells. The machinery that copies DNA, called the replisome, is a complex of dozens of proteins. If it is not properly disassembled after replication finishes, the consequences can include genetic disease, cancer, and premature ageing. Yet the mechanism of replisome disassembly has never been studied in human cells. This project will be the first to describe how replisome disassembly is accomplished and coordinated in human cells. The researchers will combine biochemical experiments using frog egg extracts with cell biology studies in immortalised human cell lines. They aim to identify new regulators of the process and determine what happens when it goes wrong. This is fundamental science. There is no immediate practical application. But understanding how cells safeguard their genome during every division is essential groundwork. Similar fundamental discoveries about DNA repair and replication have, over decades, directly informed cancer therapies and genetic diagnostics. A deeper grasp of replisome disassembly could eventually open new avenues for targeting diseases driven by genome instability.

View original technical description
Cell division requires the accurate duplication of all genetic information. DNA replication is precisely regulated as mistakes can lead to severe consequences, such as genetic disease, cancer and premature ageing. Surprisingly, despite over six decades of research, little is known about how eukaryotic replication is completed and the replisome disassembled. It is crucial that we understand this essential stage of the replication reaction so we can fully comprehend the consequences of its deregulation and to be able to exploit this for benefit of human health. Importantly, the execution and regulation of this process has never been studied in human cells. This proposal will elucidate how replisome disassembly is accomplished and coordinated in human cells, identify and characterise novel regulators of replisome disassembly and to determine the consequences of its disruption for cell biology. To deliver these answers we will combine biochemical approaches using Xenopus laevis egg extract model system and cell biology in immortalized human cell lines. The outcomes of this work will be a first description of replisome disassembly in human cells, providing a much better understanding of the mechanism of this process and demonstration the importance of its precise execution for genome stability.

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Researchers

Agnieszka Gambus (EPMC Awardee)

Related Research

Grants with similar aims, by meaning.

Investigating eukaryotic replisome dynamics at the single molecule level
Cryo-EM studies of a metazoan replisome captured ex vivo during elongation and termination
Novel Genome Integrity Pathways that regulate DNA Replication Termination in Metazoa
Purification and characterisation of a novel dominant initiation factor for chromosomal DNA replication
Roles of ubiquitin and SUMO during chromosomal DNA replication.

Original classification

Investigator Award in Science

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