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Generating a large population of Ds gene-trap and activation trap insertions in the Arabidopsis genome

ReferenceFGT11378
Principal Investigator / Supervisor Professor Michael Bevan
Co-Investigators /
Co-Supervisors
Professor George Coupland, Professor Dame Caroline Dean
Institution John Innes Centre
DepartmentCell and Develop Biology
Funding typeResearch
Value (£) 429,678
StatusCompleted
TypeResearch Grant
Start date 01/12/1999
End date 01/12/2002
Duration36 months

Abstract

The planned work aims to generate up to 30,000 new gene disruptions in the Arabidopsis genome using a novel strategy that exploits Ds transposons to insert preferentially within 1-2 Mb of the launching pad. Regions of interest can be saturated with transposon insertions, and a wide distribution of high-density insertions in the genome can also be made using mapped launching pads. Transposons that reveal cell-specific and quantitative expression levels of disrupted genes, and that over-expresses target genes will be used. A database showing expression patterns, phenotypes and the sequence of insertion sites will be available from the NASC.

Summary

unavailable
Committee Closed Committee - Engineering & Biological Systems (EBS)
Research TopicsX – not assigned to a current Research Topic
Research PriorityX – Research Priority information not available
Research Initiative Functional Genomics Toolkit (FGT) [1998]
Funding SchemeX – not Funded via a specific Funding Scheme
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