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      sel-10, a negative regulator of lin-12 activity in Caenorhabditis elegans, encodes a member of the CDC4 family of proteins.

      Genes & development
      Amino Acid Sequence, Animals, Base Sequence, Caenorhabditis elegans, genetics, metabolism, Caenorhabditis elegans Proteins, Cell Cycle Proteins, chemistry, Cell Differentiation, physiology, Cell Transformation, Neoplastic, Cloning, Molecular, DNA, Complementary, F-Box Proteins, Gene Dosage, Genes, Helminth, Helminth Proteins, Humans, Membrane Proteins, Mice, Molecular Sequence Data, Mutation, Proto-Oncogene Proteins, Receptors, Cell Surface, Receptors, Notch, Sequence Homology, Amino Acid, Signal Transduction, Ubiquitin-Protein Ligases, Ubiquitins

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          Abstract

          Mutations that influence lin-12 activity in Caenorhabditis elegans may identify conserved factors that regulate the activity of lin-12/Notch proteins. We describe genetic evidence indicating that sel-10 is a negative regulator of lin-12/Notch-mediated signaling in C. elegans. Sequence analysis shows that SEL-10 is a member of the CDC4 family of proteins and has a potential human ortholog. Coimmunoprecipitation data indicate that C. elegans SEL-10 complexes with LIN-12 and with murine Notch4. We propose that SEL-10 promotes the ubiquitin-mediated turnover of LIN-12/Notch proteins, and discuss potential roles for the regulation of lin-12/Notch activity by sel-10 in cell fate decisions and tumorigenesis.

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