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      Spatiotemporal gene expression targeting with the TARGET and gene-switch systems in Drosophila.

      Science's STKE : signal transduction knowledge environment
      5' Flanking Region, genetics, Animals, Animals, Genetically Modified, Drosophila melanogaster, Gene Expression Regulation, Gene Expression Regulation, Developmental, Gene Targeting, methods, Genes, Insect, Genes, Switch, drug effects, Genetic Vectors, Larva, Mifepristone, pharmacology, Muscles, chemistry, metabolism, Myosin Heavy Chains, Phenotype, Promoter Regions, Genetic, Regulatory Sequences, Nucleic Acid, Repressor Proteins, Sucrose, Transcriptional Activation, Transgenes

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          Abstract

          Targeted gene expression has become a standard technique for the study of biological questions in Drosophila. Until recently, transgene expression could be targeted in the dimension of either time or space, but not both. Several new systems have recently been developed to direct transgene expression simultaneously in both time and space. We describe here two such systems that we developed in our laboratory. The first system provides a general method for temporal and regional gene expression targeting (TARGET) with the conventional GAL4-upstream activator sequence (UAS) system and a temperature-sensitive GAL80 molecule, which represses GAL4 transcriptional activity at permissive temperatures. The second system, termed Gene-Switch, is based on a GAL4-progesterone receptor chimera that is hormone-inducible. We have used both systems for simultaneous spatial and temporal rescue of memory dysfunction in the rutabaga (rut) memory mutant of Drosophila. In this protocol, we provide guidelines for the use of these two novel systems, which should have general utility in studying Drosophila biology and in using the fly as a model for human disease.

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            Tight control of gene expression in mammalian cells by tetracycline-responsive promoters.

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              P[Switch], a system for spatial and temporal control of gene expression in Drosophila melanogaster.

              We have developed a method for turning on and off the expression of transgenes within Drosophila in both time and space. Two different enhancer detector elements carrying an RU486-inducible form of the yeast transcription factor GAL4 were constructed and used to generate enhancer detector lines. These lines were screened for RU486-inducible reporter gene expression in the adult head. We identified lines that exhibit inducible expression in many cell and tissue types, verifying that the elements respond to nearby enhancers. No expression was detected in the absence of the ligand. The P[Switch1] element responded to genomic enhancers less efficiently than P[Switch2] but produced more specific patterns of expression. Two P[Switch] lines were used to ablate fat body tissue in adult females through the induced expression of diphtheria toxin. These females were sterile, which correlates with fat body loss, and they died prematurely.
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