Award details

Defining the molecular phenotype of dopaminergic precursor cells: Identification of candidates for cell manipulation in vitro

ReferenceBBS/E/B/0000L478
Principal Investigator / Supervisor Dr Nicholas Allen
Co-Investigators /
Co-Supervisors
Institution Babraham Institute
DepartmentBabraham Institute Department
Funding typeResearch
Value (£) 50,368
StatusCompleted
TypeInstitute Project
Start date 01/04/2001
End date 13/03/2004
Duration35 months

Abstract

Development of the brain dopamine systems are critical for motor and cognitive functions of the brain. Of particular interest are the dopamine, DA, neurons of the midbrain that project to the forebrain to form the nigrostriatal pathway, deficits and degeneration of which leads to the development of severe neurological disorders including Parkinsons disease. Understanding the embryological and molecular mechanisms by which these neurons develop is seen as fundamental to underpin research towards the development of novel therapies. This project aims to define the molecular phenotype of wild-type precursor cells to the midbrain dopamine neurons, and subsequently to test the developmental functions of genes identified. We are using a powerful strategy in which the dopamine precursor cell populations are purified from the embryo and then subjected to a range of functional genomics analyses to determine the profile of all genes expressed in these cells. This approach will not only lead to the identification of novel genes involved in DA neuron development, but perhaps more importantly it will identify patterns of gene expression which will give us greater insight into the gene interactions involved in executing this specific developmental pathway.

Summary

unavailable
Committee Closed Committee - Biochemistry & Cell Biology (BCB)
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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