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      Regulation of the Hedgehog and Wingless signalling pathways by the F-box/WD40-repeat protein Slimb.

      Nature
      Amino Acid Sequence, Animals, Animals, Genetically Modified, Armadillo Domain Proteins, Cell Cycle Proteins, chemistry, genetics, metabolism, Cloning, Molecular, Cyclic AMP-Dependent Protein Kinases, DNA-Binding Proteins, Drosophila, Drosophila Proteins, F-Box Proteins, GTP-Binding Proteins, Gene Expression Regulation, Developmental, Hedgehog Proteins, Insect Proteins, Male, Molecular Sequence Data, Mutation, Proto-Oncogene Proteins, Signal Transduction, Trans-Activators, Transcription Factors, Ubiquitin-Protein Ligases, Ubiquitins, Wing, embryology, Wnt1 Protein, beta-Transducin Repeat-Containing Proteins

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          Abstract

          Members of the Hedgehog (Hh) and Wnt/Wingless (Wg) families of secreted proteins control many aspects of growth and patterning during animal development. Hh signal transduction leads to increased stability of a transcription factor, Cubitus interruptus (Ci), whereas Wg signal transduction causes increased stability of Armadillo (Arm/beta-catenin), a possible co-factor for the transcriptional regulator Lef1/TCF. Here we describe a new gene, slimb (for supernumerary limbs), which negatively regulates both of these signal transduction pathways. Loss of function of slimb results in a cell-autonomous accumulation of high levels of both Ci and Arm, and the ectopic expression of both Hh- and Wg- responsive genes. The slimb gene encodes a conserved F-box/WD40-repeat protein related to Cdc4p, a protein in budding yeast that targets cell-cycle regulators for degradation by the ubiquitin/proteasome pathway. We propose that Slimb protein normally targets Ci and Arm for processing or degradation by the ubiquitin/proteasome pathway, and that Hh and Wg regulate gene expression at least in part by inducing changes in Ci and Arm, which protect them from Slimb-mediated proteolysis.

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