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- W2035220761 abstract "Regulation of Notch signaling is critical to development and maintenance of most eukaryotic organisms. The Notch receptors and ligands are integral membrane proteins and direct cell–cell interactions are needed to activate signaling. Ligand-expressing cells activate Notch signaling through an unusual mechanism involving Notch proteolysis to release the intracellular domain from the membrane, allowing the Notch receptor to function directly as the downstream signal transducer. In the absence of ligand, the Notch receptor is maintained in an autoinhibited, protease resistant state. Genetic studies suggest that Notch ligands require ubiquitylation, epsin endocytic adaptors and dynamin-dependent endocytosis for signaling activity. Here we discuss potential models and supporting evidence to account for the absolute requirement for ligand endocytosis to activate signaling in Notch cells. Specifically, we focus on a role for ligand-mediated endocytic force to unfold Notch, override the autoinhibited state, and activate proteolysis to direct Notch-specific cellular responses." @default.
- W2035220761 created "2016-06-24" @default.
- W2035220761 creator A5053113346 @default.
- W2035220761 creator A5073460010 @default.
- W2035220761 creator A5080777821 @default.
- W2035220761 date "2012-06-01" @default.
- W2035220761 modified "2023-10-10" @default.
- W2035220761 title "Notch ligand endocytosis: Mechanistic basis of signaling activity" @default.
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- W2035220761 doi "https://doi.org/10.1016/j.semcdb.2012.01.011" @default.
- W2035220761 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3507467" @default.
- W2035220761 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/22306180" @default.
- W2035220761 hasPublicationYear "2012" @default.
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