Improved T-DNA vector for tagging plant promoters via high-throughput luciferase screening

Transferred DNA (T-DNA) tagging is a powerful tool for tagging and in planta characterization of plant genes on a genome-wide scale. An improved promoter tagging vector is described here, which contains the codon-optimized luciferase ( ) reporter gene 31 bpfrom the right border of the T-DNA. Compare...

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Veröffentlicht in:BioTechniques 2005-05, Vol.38 (5), p.763-770
Hauptverfasser: Remy, Serge, Bertcoemans, Els Thiry, Windelinckx, Saskia, Swennen, Rony, Sági, László
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Sprache:eng
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Zusammenfassung:Transferred DNA (T-DNA) tagging is a powerful tool for tagging and in planta characterization of plant genes on a genome-wide scale. An improved promoter tagging vector is described here, which contains the codon-optimized luciferase ( ) reporter gene 31 bpfrom the right border of the T-DNA. Compared to the wild-type luciferase gene, this construct provides significantly increased reporter gene expression and a 40 times higher tagging frequency. The utility of the construct is demonstrated in banana, a tropical monocot species, by screening embryogenic cell colonies and regenerated plants with an ultrasensitive charged-coupled device (CCD) camera. The improved vector resulted in a luciferase activation frequency of 2.5% in 19,000 cell colonies screened. Detailed molecular analysis of flanking DNA sequences in a tagged line revealed insertion of the luciferase tag in a novel gene with near-constitutive expression.
ISSN:0736-6205
1940-9818
DOI:10.2144/05385RR01