Mammalian homologs of seven in absentia regulate DCC via the ubiquitin-proteasome pathway.

DCC (deleted in colorectal cancer) is postulated to function as transmembrane receptor for the axon and cell guidance factor netrin-1. We report here that the DCC cytoplasmic domain binds to proteins encoded by mammalian homologs of the Drosophila seven in absentia (sina) gene, as well as Drosophila Sina. Sina has ...
a critical role in R7 photoreceptor development and shows upward of 85% amino acid identity with its mammalian homologs (termed Siahs), but the function of the Sina/Siah proteins has not been defined. We sought, therefore, to characterize further their interaction with DCC. Immunofluorescence studies suggested the Sina/Siah proteins localized predominantly in the cytoplasm and in association with DCC. DCC was found to be ubiquitinated and the Sina/Siah proteins regulated its expression. Proteasome inhibitors blocked the effects of Sina/Siah on DCC, and the Sina/Siah proteins interacted with ubiquitin-conjugating enzymes (Ubcs). A mutant Siah protein lacking the amino-terminal Ubc-binding sequences complexed with DCC, but did not degrade it. The in vivo interaction between Sina/Siah and DCC was confirmed through studies of transgenic Drosophila lines in which DCC and Sina were ectopically expressed in the eye. Taken together, the data imply that the Sina/Siah proteins regulate DCC and perhaps other proteins via the ubiquitin-proteasome pathway.
Mesh Terms:
Animals, Animals, Genetically Modified, CHO Cells, COS Cells, Cell Adhesion Molecules, Cell Line, Cricetinae, Drosophila, Gene Library, Genes, DCC, Glioblastoma, Humans, Mammals, Nuclear Proteins, Receptors, Cell Surface, Recombinant Fusion Proteins, Saccharomyces cerevisiae, Transfection, Transplantation, Heterologous, Tumor Cells, Cultured, Tumor Suppressor Proteins, Ubiquitin-Protein Ligases
Genes Dev.
Date: Oct. 15, 1997
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