Numb Is an Endocytic Protein
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Open Access
- 11 December 2000
- journal article
- Published by Rockefeller University Press in The Journal of cell biology
- Vol. 151 (6), 1345-1352
- https://doi.org/10.1083/jcb.151.6.1345
Abstract
Numb is a protein that in Drosophila determines cell fate as a result of its asymmetric partitioning at mitosis. The function of Numb has been linked to its ability to bind and to biologically antagonize Notch, a membrane receptor that also specifies cell fate. The biochemical mechanisms underlying the action of Numb, however, are still largely unknown. The wide pattern of expression of Numb suggests a general function in cellular homeostasis that could be additional to, or part of, its action in fate determination. Such a function could be endocytosis, as suggested by the interaction of Numb with Eps15, a component of the endocytic machinery. Here, we demonstrate that Numb is an endocytic protein. We found that Numb localizes to endocytic organelles and is cotrafficked with internalizing receptors. Moreover, it associates with the appendage domain of α adaptin, a subunit of AP2, a major component of clathrin-coated pits. Finally, fragments of Numb act as dominant negatives on both constitutive and ligand-regulated receptor-mediated internalization, suggesting a general role for Numb in the endocytic process.Keywords
This publication has 33 references indexed in Scilit:
- The EH NetworkExperimental Cell Research, 1999
- Contact-Dependent Inhibition of Cortical Neurite Growth Mediated by Notch SignalingScience, 1999
- A Structural Explanation for the Binding of Multiple Ligands by the α-Adaptin Appendage DomainCell, 1999
- Notch Signaling: Cell Fate Control and Signal Integration in DevelopmentScience, 1999
- Mammalian NUMB is an evolutionarily conserved signaling adapter protein that specifies cell fateCurrent Biology, 1996
- Control of Daughter Cell Fates during Asymmetric Division: Interaction of Numb and NotchNeuron, 1996
- The Ear of α-Adaptin Interacts with the COOH-terminal Domain of the Eps15 ProteinPublished by Elsevier ,1996
- The tyrosine kinase substrate eps15 is constitutively associated with the plasma membrane adaptor AP-2.The Journal of cell biology, 1995
- Asymmetric segregation of Numb and Prospero during cell divisionNature, 1995
- Notch SignalingScience, 1995