Notch signaling influences development and maintenance of the nervous system through directing the specification of neural progenitors into neurons and glia, as well as regulating neurite morphogenesis and synaptic interactions. Notch was first identified as a neurogenic gene, yet activation of Notch receptors by Delta/Serrate/Lag2 (DSL) ligands regulates the differentiation of a wide variety of neuronal and non-neuronal cell types. Moreover, Notch signaling has been linked to certain cancers, inherited human syndromes and neurodegenerative diseases. Although a role for Notch in these different processes is certain, the molecular mechanisms of ligand-induced Notch signaling are not well defined. To biochemically and molecularly characterize ligand-Notch interactions and downstream signaling events we have developed ligand-binding and cell co-culture assays in which components of the Notch signaling system can be readily manipulated and studied. Importantly, these co-culture systems measure Notch signaling induced by ligand, which is more reflective of physiological Notch signaling than the widely used constitutively active forms of Notch. Our studies have identified a noncanonical Notch signaling pathway that differs from the """"""""core"""""""" Notch signaling pathway both in the Notch isoform and downstream effector, CSL (CBF-1, Su(H), Lag-1), activated by ligand, in addition, we have identified sequences within both the DSL ligand and Notch receptor proteins that confer ligand-receptor specificity and have demonstrated that the glycosyltransferase fringe differentially modulates ligand-induced Notch signaling as first described for Drosophila. Finally, we have discovered that the DSL family member, Delta3, does not activate Notch signaling but rather functions to inhibit ligand-induced Notch signaling. The experiments proposed in this application are logical extensions of our previous findings.
Three aims are proposed to (1) define the requirements and downstream targets of CSL-independent Notch signaling; (2) characterize the effects of different ligand-receptor combinations on Notch signaling; and (3) characterize the inhibitory effects of Delta3 on ligand-induced Notch signaling. Information obtained using these approaches will extend our current understanding of the molecular mechanisms of Notch signal transduction and provide clues as to how this signaling system regulates a diverse array of cellular processes both in the embryo and in the adult.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Method to Extend Research in Time (MERIT) Award (R37)
Project #
2R37NS031885-10A1
Application #
6684051
Study Section
Molecular, Cellular and Developmental Neurosciences 2 (MDCN)
Program Officer
Leblanc, Gabrielle G
Project Start
1994-01-01
Project End
2008-07-31
Budget Start
2003-08-01
Budget End
2004-07-31
Support Year
10
Fiscal Year
2003
Total Cost
$360,013
Indirect Cost
Name
University of California Los Angeles
Department
Biochemistry
Type
Schools of Medicine
DUNS #
092530369
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
Weinmaster, Gerry; Fischer, Janice A (2011) Notch ligand ubiquitylation: what is it good for? Dev Cell 21:134-44
D'Souza, Brendan; Meloty-Kapella, Laurence; Weinmaster, Gerry (2010) Canonical and non-canonical Notch ligands. Curr Top Dev Biol 92:73-129
McGill, Melanie A; Dho, Sascha E; Weinmaster, Gerry et al. (2009) Numb regulates post-endocytic trafficking and degradation of Notch1. J Biol Chem 284:26427-38
Bozkulak, Esra Cagavi; Weinmaster, Gerry (2009) Selective use of ADAM10 and ADAM17 in activation of Notch1 signaling. Mol Cell Biol 29:5679-95
D'Souza, B; Miyamoto, A; Weinmaster, G (2008) The many facets of Notch ligands. Oncogene 27:5148-67
Nichols, James T; Miyamoto, Alison; Weinmaster, Gerry (2007) Notch signaling--constantly on the move. Traffic 8:959-69
Nichols, James T; Miyamoto, Alison; Olsen, Samantha L et al. (2007) DSL ligand endocytosis physically dissociates Notch1 heterodimers before activating proteolysis can occur. J Cell Biol 176:445-58
Miyamoto, Alison; Lau, Rhiana; Hein, Patrick W et al. (2006) Microfibrillar proteins MAGP-1 and MAGP-2 induce Notch1 extracellular domain dissociation and receptor activation. J Biol Chem 281:10089-97
Yang, Liang-Tung; Nichols, James T; Yao, Christine et al. (2005) Fringe glycosyltransferases differentially modulate Notch1 proteolysis induced by Delta1 and Jagged1. Mol Biol Cell 16:927-42
Nehring, Leslie C; Miyamoto, Alison; Hein, Patrick W et al. (2005) The extracellular matrix protein MAGP-2 interacts with Jagged1 and induces its shedding from the cell surface. J Biol Chem 280:20349-55

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