<i>Transposon Display</i> identifies individual transposable elements in high copy number lines

Dirk Va(Ghent University), Ning De(Ghent University), Nick Van den Broeck(Ghent University), Tamara Maes(Ghent University), Matt Sauer(Ghent University), Jan Zethof(Ghent University), Peter D. Currie(Ghent University), E Keukeleire(Ghent University), Mariëlla D’hauw(Ghent University), Marc Va(Ghent University), N Montagu(Ghent University), Tom Gerats(Ghent University)
The Plant Journal
January 1, 1998
Cited by 177Open Access
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Abstract

The dTph1 transposable element family of Petunia hybrida line W138 consists of between 100 and 200 members. A strategy that allows simultaneous detection of individual elements is described. Sequences flanking dTph1 elements are amplified by means of a ligation-mediated PCR. The resulting fragments are locus-specific and can be analysed by polyacrylamide gel electrophoresis. One of the applications of Transposon Display is the isolation of dTph1-tagged genes. Fragments that co-segregate with a mutant phenotype can be extracted from the gel and reamplified, providing access to tagged genes, as demonstrated in a reconstruction experiment. Data on the molecular identification of a phenotypic mutant, isolated in a random tagging experiment is also presented. Upon sequencing, the obtained candidate fragment was found to be identical to part of the previously identified Fbp1 gene.


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