Notch Signaling: The Core Pathway and Its Posttranslational Regulation

被引:587
作者
Fortini, Mark E. [1 ]
机构
[1] Thomas Jefferson Univ, Kimmel Canc Ctr, Dept Biochem & Mol Biol, Philadelphia, PA 19107 USA
关键词
ASYMMETRIC CELL-DIVISION; GAMMA-SECRETASE CLEAVAGE; LIGAND-BINDING DOMAIN; O-FUCOSYL-TRANSFERASE; GENE BIG BRAIN; DROSOPHILA-MELANOGASTER; C-ELEGANS; PROTEIN O-FUCOSYL-TRANSFERASE-1; CAENORHABDITIS-ELEGANS; INTRACELLULAR DOMAIN;
D O I
10.1016/j.devcel.2009.03.010
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Notch signaling controls numerous cell-fate specification events in multicellular organisms, and dysregulated Notch signaling causes several diseases with underlying developmental defects. A key step in Notch receptor activation is its intramembrane proteolysis, which releases an intracellular fragment that participates directly in transcriptional regulation of nuclear target genes. Despite the apparent simplicity of this mechanism, a host of posttranslational processes regulate Notch activity during its synthesis and secretion, ligand-dependent activation at the surface, endocytic trafficking, and degradation. This review describes the core developmental logic of Notch signaling and how regulatory mechanisms tailor Notch pathway outputs to specific developmental scenarios.
引用
收藏
页码:633 / 647
页数:15
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