Completed Genetics & Molecular Biology Cells, Biochemistry & Physiology

Molecular insights into ubiquitin remodelling factor p97(VCP) in DNA damage response and genome stability

In plain English

AI plain-English summary

Every cell in your body tags old or damaged proteins with a molecular handle called ubiquitin, then feeds them to a recycling machine called the proteasome. This grant will investigate how that recycling process works specifically when cells are repairing broken DNA. The problem is that we know the ubiquitin tag is attached to proteins, but we do not understand exactly when or how this happens during DNA repair. Since faulty DNA repair can trigger cancer, and since radio- and chemotherapy work by deliberately damaging cancer cells’ DNA, understanding this recycling step could reveal why some tumours resist treatment. If this research succeeds, it could open the door to designing therapies that make radiation and chemotherapy more effective by controlling how cells recycle the proteins that fix the damage those treatments cause. This is fundamental science—the work will not produce a new drug tomorrow. But similar fundamental discoveries about how cells handle proteins have already led to cancer drugs that block the proteasome itself, showing how a deeper grasp of recycling machinery can eventually change treatment.

View original technical description
Your body is built of billions of cells, and they all have to work as a team. Almost everything a cell does involves a protein. Proteins relay decisions, build structures, translate genetic instructions, repair damage, and carry signals. So it is not surprising that cancer is marked by proteins not working properly. Sometimes the proteins fail; sometimes they do their job too well, or do it at the wrong time. Proteins are created and recycled constantly; this makes sure that proteins do not get old and damaged. The balance between making and recycling proteins is kept in tight check, making sure that the amount of a given protein is just right. Our work focuses on the way cells recycle proteins. We know that proteins that are old or not needed are labelled for recycling with a tag called ubiquitin. Huge recycling machines called proteasomes grab hold of the ubiquitin handle and recycle the attached protein. We don't know in detail when and how the ubiquitin label is attached. We want to know how this works during the process of repairing damaged DNA. Damaged DNA can be a starting point for cancer; but it's also the key to effective radio- and chemotherapy. If we knew how cells recycle the proteins that repair radiation and chemotherapeutic damage to DNA then we would be able to design ways to make radio- and chemotherapy more effective. This grant will fund research to improve our understanding of the proteins involved in DNA damage repair and the processes that recycle them.

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Related Research

Grants with similar aims, by meaning.

Post-Translational Modifications in the Radiation Damage Response
Ubiquitylation within and beyond the DNA damage response
Dissecting the role of tubulin acetylation in DNA repair to improve response to PARPi
Investigating how cells repair DNA damage during mitosis
Determining how global genome nucleotide excision repair promotes efficient removal of DNA damage from chromatin

Original classification

Research Grant

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