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piggyBac-Based Insertional Mutagenesis and Enhancer Detection as a Tool for Functional Insect Genomics
Carsten Horna, Nils Offena, Sverker Nystedtb, Udo Häckerb, and Ernst A. Wimmeraa Lehrstuhl für Genetik, Universität Bayreuth, 95447 Bayreuth, Germany
b Department of Cell and Molecular Biology, Lund University, 22184 Lund, Sweden
Corresponding author: Ernst A. Wimmer, 95447 Bayreuth, Germany., ernst.wimmer{at}uni-bayreuth.de (E-mail)
Communicating editor: T. C. KAUFMAN
1-tubulin promoter. As primary reporters in the piggyBac mutator elements, we employed the heterologous transactivators GAL4
or tTA. To identify larval and adult enhancer detectors, strains carrying UASp-EYFP or TRE-EYFP as secondary reporter elements were used. Tissue-specific enhancer activities were readily observed in the GAL4
/UASp-based systems, but only rarely in the tTA/TRE system. Novel autosomal insertions were recovered with an average jumping rate of 80%. Of these novel insertions, 3.8% showed homozygous lethality, which was reversible by piggyBac excision. Insertions were found in both coding and noncoding regions of characterized genes and also in noncharacterized and non-P-targeted CG-number genes. This indicates that piggyBac will greatly facilitate the intended saturation mutagenesis in Drosophila.
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