Completed Genetics & Molecular Biology Cells, Biochemistry & Physiology

DNA replication forks and checkpoints

In plain English

AI plain-English summary

Every time a cell copies its DNA, the machinery doing the copying can jam—and when it does, a molecular alarm system must decide whether to fix the jam or let the cell die. This project aims to understand exactly how that alarm system works. The problem is that scientists know the parts of this DNA replication checkpoint—the proteins involved and the general shape of the signalling pathway—but not how it detects such a wide variety of jams (called replication fork stalls) and responds through a single common route. Without this understanding, it is impossible to predict when the system fails, which is a hallmark of cancer cells. This is fundamental science with no immediate practical application. The researchers will use a test-tube system that rebuilds DNA replication from purified proteins, adding checkpoint components and custom DNA templates to watch the activation process in molecular detail. They will also investigate a newly discovered protein, HLTF, whose loss paradoxically prevents permanent fork arrest—suggesting it creates a toxic intermediate that the checkpoint normally blocks. Understanding this mechanism could eventually reveal why some cancers become resistant to chemotherapy drugs that deliberately stall replication forks.

View original technical description
The DNA replication checkpoint senses perturbation of DNA replication forks by a wide variety of agents. We know the protein components and the overall architecture of the checkpoint pathways, but we do not understand how very different fork stalling events can signal via a common pathway. The first aim of this proposal is to use the fully reconstituted DNA replication system we have developed together with purified checkpoint proteins and defined DNA templates to elucidate in molecular detail the mechanisms by which the checkpoint pathway is activated. One of the main functions of this checkpoint is to prevent irreversible replication fork arrest (IRFA). From a whole genome siRNA screen, we have recently found that loss of the HLTF DNA translocase suppresses IRFA. Furthermore, we have found evidence that HLTF generates a toxic recombination intermediate and that this is conserved in yeast. Our second aim is to use genetics in human cells along with biochemistry with yeast proteins to understand how IRFA is generated and how the DNA damage checkpoint protects forks from IRFA.

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Researchers

John Diffley (EPMC Awardee)

Related Research

Grants with similar aims, by meaning.

Deciphering the mechanism of irreversible replication fork arrest
Analysis by ChIP-sequencing of the regulation of DNA replication fork progression by checkpoint kinases during replication stress
Elucidation of checkpoint kinase interactions with the replisome
Novel mechanisms through which the S-phase checkpoint pathway preserves genome integrity
Decision Making at Protected Replication Forks

Original classification

Investigator Award in Science

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