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Investigation of the role of the human FEN1 gene in genomic instability using inducible ribozyme gene ablation

ReferenceG11906
Principal Investigator / Supervisor Professor Kay Davies
Co-Investigators /
Co-Supervisors
Institution University of Oxford
DepartmentHuman Anatomy and Genetics
Funding typeResearch
Value (£) 145,708
StatusCompleted
TypeResearch Grant
Start date 01/05/2000
End date 01/05/2002
Duration24 months

Abstract

Genetic instability in triplet arrays is of great biological interest as it represents a unique pathway which generates alleles with an increased mutational propensity. Attempts to model such instability in the mouse have only limited success but yeast studies have identified the FEN1 gene as playing a critical role in the fidelity of repeat array replication, suggesting that variations in its expression or activity might underlie instability in humans. We propose to examine the role of FEN1 in triplet array instability in human cells using state of the art gene ablation techniques. This will provide insights into human genome instability and serve as a model system in which similar genes can be easily studied.

Summary

unavailable
Committee Closed Committee - Genes & Developmental Biology (GDB)
Research TopicsX – not assigned to a current Research Topic
Research PriorityX – Research Priority information not available
Research Initiative X - not in an Initiative
Funding SchemeX – not Funded via a specific Funding Scheme
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