Numb Regulates Post-endocytic Trafficking and Degradation of Notch1

被引:184
作者
McGill, Melanie A. [1 ,2 ]
Dho, Sascha E. [1 ]
Weinmaster, Gerry [3 ]
McGlade, C. Jane [1 ,2 ]
机构
[1] Hosp Sick Children, Arthur & Sonia Labatt Brain Tumour Res Ctr, Toronto, ON M5G 1X8, Canada
[2] Univ Toronto, Dept Med Biophys, Toronto, ON M5G 1X8, Canada
[3] Univ Calif Los Angeles, David Geffen Sch Med, Dept Biol Chem, Los Angeles, CA 90095 USA
基金
美国国家卫生研究院;
关键词
SPECIFY CELL FATE; MAMMALIAN NUMB; LIGAND ENDOCYTOSIS; UBIQUITIN LIGASE; DOWN-REGULATION; ASYMMETRIC LOCALIZATION; ALPHA-ADAPTIN; PROTEIN; RECEPTOR; ACTIVATION;
D O I
10.1074/jbc.M109.014845
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Notch is a transmembrane receptor that controls cell fate decisions during development and tissue homeostasis. Both activation and attenuation of the Notch signal are tightly regulated by endocytosis. The adaptor protein Numb acts as an inhibitor of Notch and is known to function within the intracellular trafficking pathways. However, a role for Numb in regulating Notch trafficking has not been defined. Here we show that mammalian Notch1 is constitutively internalized and trafficked to both recycling and late endosomal compartments, and we demonstrate that changes in Numb expression alter the dynamics of Notch1 trafficking. Overexpression of Numb promotes sorting of Notch1 through late endosomes for degradation, whereas depletion of Numb facilitates Notch1 recycling. Numb mutants that do not interact with the ubiquitin-protein isopeptide ligase, Itch, or that lack motifs important for interaction with endocytic proteins fail to promote Notch1 degradation. Our data suggest that Numb inhibits Notch1 activity by regulating post-endocytic sorting events that lead to Notch1 degradation.
引用
收藏
页码:26427 / 26438
页数:12
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