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Generating a large population of Ds gene-trap and activation trap insertions in the Arabidopsis genome
Reference
FGT11378
Principal Investigator / Supervisor
Professor Michael Bevan
Co-Investigators /
Co-Supervisors
Professor George Coupland
,
Professor Dame Caroline Dean
Institution
John Innes Centre
Department
Cell and Develop Biology
Funding type
Research
Value (£)
429,678
Status
Completed
Type
Research Grant
Start date
01/12/1999
End date
01/12/2002
Duration
36 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 Topics
X – not assigned to a current Research Topic
Research Priority
X – Research Priority information not available
Research Initiative
Functional Genomics Toolkit (FGT) [1998]
Funding Scheme
X – not Funded via a specific Funding Scheme
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