1. Use of promoter fusions inDrosophila genetics: Characterization of a YP1-ADH fusion gene
- Author
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Barry S. Aprison, J. Jose Bonner, and David L. Osterbur
- Subjects
Genotype ,Genetic Vectors ,Pair-rule gene ,Biology ,Fusion gene ,Gene cluster ,Gene expression ,Genetics ,Animals ,Cloning, Molecular ,Promoter Regions, Genetic ,Gene ,Alleles ,Selectable marker ,Reporter gene ,Egg Proteins ,Alcohol Dehydrogenase ,Cell Biology ,Drosophila melanogaster ,Genes ,Mutation ,Female ,Plasmids ,Developmental Biology ,Genetic screen - Abstract
In Drosophila melanogaster the yolk protein (YP) genes are normally expressed only in the fat body and follicular epithelium of adult females--never in males or in larvae. We describe here a first step toward a genetic examination of the developmental controls that restrict the activity of the YP genes to adult female tissues. A YP1 promoter that contains the tissue-, temporal-, and sex-specific controlling elements for expression was fused to the reporter gene, alcohol dehydrogenase (Adh). The gene fusion was transformed into an Adh-deficient genotype. As assayed by a number of criteria, that the fusion gene is expressed in the same physiological manner as the endogenous yolk protein genes. The fusion gene's activity is modulated in trans by a temperature-sensitive allele of the sex determination gene, tra-2. The Adh enzyme serves as a selectable marker and therefore these flies are suitable for use in genetic screens for trans-acting mutations that affect the expression of the yolk protein genes.
- Published
- 1989
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