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Drosophila APC2 is a cytoskeletally-associated protein that regulates wingless signaling in the embryonic epidermis.

The tumor suppressor adenomatous polyposis coli (APC) negatively regulates Wingless (Wg)/Wnt signal transduction by helping target the Wnt effector beta-catenin or its Drosophila homologue Armadillo (Arm) for destruction. In cultured mammalian cells, APC localizes to the cell cortex near the ends of microtubules. Drosophila APC (dAPC) negatively regulates Arm signaling, but only in a limited set of tissues. We describe a second fly APC, dAPC2, which binds Arm and is expressed in a broad spectrum of tissues. dAPC2's subcellular localization revealed colocalization with actin in many but not all cellular contexts, and also suggested a possible interaction with astral microtubules. For example, dAPC2 has a striking asymmetric distribution in neuroblasts, and dAPC2 colocalizes with assembling actin filaments at the base of developing larval denticles. We identified a dAPC2 mutation, revealing that dAPC2 is a negative regulator of Wg signaling in the embryonic epidermis. This allele acts genetically downstream of wg, and upstream of arm, dTCF, and, surprisingly, dishevelled. We discuss the implications of our results for Wg signaling, and suggest a role for dAPC2 as a mediator of Wg effects on the cytoskeleton. We also speculate on more general roles that APCs may play in cytoskeletal dynamics.

Pubmed ID: 10491393 RIS Download

Mesh terms: Actins | Amino Acid Sequence | Animals | Armadillo Domain Proteins | Cloning, Molecular | Cytoskeletal Proteins | Cytoskeleton | Drosophila Proteins | Drosophila melanogaster | Epidermis | Epistasis, Genetic | Female | Genes, Insect | Humans | Insect Proteins | Larva | Male | Molecular Sequence Data | Mutation | Neurons | Phosphorylation | Proto-Oncogene Proteins | Signal Transduction | Spindle Apparatus | Trans-Activators | Transcription Factors | Tumor Cells, Cultured | Wnt1 Protein

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Associated grants

  • Agency: NCI NIH HHS, Id: F32 CA079172
  • Agency: NIGMS NIH HHS, Id: R01 GM047857
  • Agency: NCI NIH HHS, Id: 1 F32 CA79172-01
  • Agency: NIGMS NIH HHS, Id: GM47857

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