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Analysis of the developmental role of Raidd an apoptotic gene whose loss of function causes embryonic lethality

ReferenceG15680
Principal Investigator / Supervisor Dr James McWhir
Co-Investigators /
Co-Supervisors
Institution The Roslin Institute
DepartmentGene Expression and Development
Funding typeResearch
Value (£) 171,724
StatusCompleted
TypeResearch Grant
Start date 04/05/2002
End date 04/05/2005
Duration36 months

Abstract

The high growth (HG) mutation was discovered in mice selected for high post-weaning gain and is associated with a 30 percent average increase in adult weight. The mutation comprises a 500kb deletion in which two genes have been identified. Knockout mice have been generated at one of these loci (Raidd). Homozygous Raidd knockout mice fail in preimplantation development. The objective of the present proposal is to determine if the interaction of Raidd with the other known gene within the deletion, Socs2, can account for the fact that loss of Raidd function in HG mice is consistent with development to term.

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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