Active Genetics & Molecular Biology Cells, Biochemistry & Physiology

Decision Making at Protected Replication Forks

In plain English

AI plain-English summary

Every time a cell copies its DNA, thousands of molecular machines called replication forks race along the chromosomes—and when they stall, a set of protective proteins must step in to stop cellular scissors from snipping the exposed DNA. This protection system is critical: several genes linked to cancer predisposition and developmental disorders encode the very proteins that guard paused forks. Yet researchers do not fully understand where, when, or how this protection works, or how cells decide whether to restart a protected fork or dismantle a broken one. This project will map those decisions at the molecular level. The team will identify which genomic locations most need protection, what triggers the protective response, and how stalled forks signal to recovery machinery. They will also examine how chromatin—the packaging of DNA—is rearranged to allow repair to proceed. This is fundamental science. There is no immediate clinical application. But the process directly suppresses genome instability, a hallmark of cancer. Understanding the molecular logic of fork protection could eventually reveal why certain tumours are vulnerable to particular therapies or become resistant, opening new avenues for treatment design.

View original technical description
The process of DNA replication is central to life. Several proteins encoded by genes important to cancer-predisposition syndromes and human development are essential when replication forks stall, preventing DNA nucleases from degrading the paused fork. The process suppresses genome instability and may be relevant to cancer therapy by determining particular therapeutic vulnerabilities and therapy resistances. However, the role, regulation and impact of replication fork protection is poorly understood, and we currently lack the knowledge of where the opportunities for improved human health in this process may lie. Using an integrated approach, we aim to address where and in response to what replication fork protection is most needed, how stalled protected and unprotected forks signal to recovery mechanisms, and how chromatin is regulated to promote recovery. We will reveal the molecular basis of decisions at protected and unprotected replication forks to define the opportunities for improved human health.

View the original record at the funder ↗

Researchers

Joanna Morris (EPMC Awardee)

Related Research

Grants with similar aims, by meaning.

Investigating the Mechanisms Controlling Homologous Recombination-Dependent DNA Replication Fork Recovery in Response to Replication Stress.
Investigating the role of DNA2 and homologous recombination in the recovery of stalled DNA replication forks
Deciphering the mechanism of irreversible replication fork arrest
Replication fork stability and fork restart
Investigating the factors that influence genome stability when replication forks encounter single-strand DNA breaks and protein roadblocks

Original classification

Discovery Award

Plain English summaries and category classifications on this site are generated by AI and may not perfectly reflect the original research.