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Microarray-mediated analysis of gene expression in the T lymphocyte lineage of the diabetes prone BB rat

ReferenceGAN13085
Principal Investigator / Supervisor Dr Geoff Butcher
Co-Investigators /
Co-Supervisors
Dr James Ross Miller
Institution Babraham Institute
DepartmentBabraham Institute Department
Funding typeResearch
Value (£) 173,312
StatusCompleted
TypeResearch Grant
Start date 01/09/2000
End date 30/06/2004
Duration46 months

Abstract

The BB rat is known to develop autoimmune insulin dependent diabetes mellitus (IDDM) at a high frequency. Two genes play a key role in this disease model: the RT1u haplotype of MHC class II and the autosomal recessive mutation lymphopenia (lyp). Lyp has been mapped within rat chromosome 4, but remains as yet uncloned. Recent work in our laboratory has indicated that lyp causes an increased level of apoptosis of mature thymocytes and hence prevents the development of a normal T cell pool with appropriate regulatory subsets. This project will use microarray technology firstly to categorise gene expression in mature thymocytes and/or naareve peripheral T cells and secondly to look for differential levels of gene expression between rats with and without the lyp mutation.

Summary

unavailable
Committee Closed Committee - Animal Sciences (AS)
Research TopicsX – not assigned to a current Research Topic
Research PriorityX – Research Priority information not available
Research Initiative Genomics in Animal Function Initiative (GAN) [1998]
Funding SchemeX – not Funded via a specific Funding Scheme
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