We propose to continue our studies on the tyrosine kinase Src (also called c-Src), the cellular homolog of the v-Src oncoprotein. Activated Src causes transformation of some cell types and cancer in animals, but can stimulate differentiation, migration, survival or apoptosis when expressed in other cell types. Because activated Src phosphorylates many different cell proteins, the specific mechanisms underlying these different cellular outcomes have been difficult to dissect. Moreover, the roles of the normal cellular Src protein have been unclear, in part due to overlapping functions between Src and other close relatives. Src activity is elevated in many human cancers, including approximately 70% of carcinomas. Understanding a novel aspect of Src biology is the general goal of this proposal. Over the past funding period, our study of a Src substrate, Dab1, led us to uncover a Src-dependent signaling pathway that regulates the migrations of neuronal precursors in the developing mammalian central nervous system. An extracellular protein, Reelin, acts via non-catalytic receptors to stimulate Src- dependent tyrosine phosphorylation of Dab1. Genetic evidence shows that tyrosine phosphorylation of Dab1 is both a cause and a consequence of activation of Src, and both events are required for downstream signaling. Reelin stimulates Dab1 binding to several identified signaling proteins, including the adaptor proteins Crk and CrkL. Reelin also stimulates Dab1 ubiquitylation and degradation, and Reelin receptor endocytosis. However, it is not yet clear whether Dab1 ubiquitylation regulates signaling or endocytbsis or is a feedback control, and it remains unclear how Dab1 degradation, Reelin endocytosis, Dab1-complex formation, and Src kinase activation link to each other and regulate neuron precursor movements in vivo. Wepropose to use genetic and biochemical approaches to uncover the mechanisms by which Src and Dab1 regulate cell migrations in vivo. We propose two broad aims: to uncover the importance of different Dab1 phosphorylation sites and signaling complexes and Dab1 degradation in Dab1 regulation and development;and to determine the specific roles of Crk, CrkL, their downstream mediator C3G, and endocytosis in signaling. By further study of this signaling process, we expect to identify principles of signal complex formation and regulation that may be relevant to other tyrosine kinase signaling pathways.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA041072-26
Application #
7990406
Study Section
Neurogenesis and Cell Fate Study Section (NCF)
Program Officer
Yassin, Rihab R,
Project Start
1986-01-01
Project End
2012-12-31
Budget Start
2011-01-01
Budget End
2012-12-31
Support Year
26
Fiscal Year
2011
Total Cost
$549,678
Indirect Cost
Name
Fred Hutchinson Cancer Research Center
Department
Type
DUNS #
078200995
City
Seattle
State
WA
Country
United States
Zip Code
98109
Teckchandani, Anjali; Laszlo, George S; Simo, Sergi et al. (2014) Cullin 5 destabilizes Cas to inhibit Src-dependent cell transformation. J Cell Sci 127:509-20
Cheng, Catherine; Ansari, Moham M; Cooper, Jonathan A et al. (2013) EphA2 and Src regulate equatorial cell morphogenesis during lens development. Development 140:4237-45
Simó, Sergi; Cooper, Jonathan A (2013) Rbx2 regulates neuronal migration through different cullin 5-RING ligase adaptors. Dev Cell 27:399-411
Matsuki, Tohru; Zaka, Mariam; Guerreiro, Rita et al. (2012) Identification of Stk25 as a genetic modifier of Tau phosphorylation in Dab1-mutant mice. PLoS One 7:e31152
Cai, Houjian; Smith, Daniel A; Memarzadeh, Sanaz et al. (2011) Differential transformation capacity of Src family kinases during the initiation of prostate cancer. Proc Natl Acad Sci U S A 108:6579-84
Jossin, Yves; Cooper, Jonathan A (2011) Reelin, Rap1 and N-cadherin orient the migration of multipolar neurons in the developing neocortex. Nat Neurosci 14:697-703
Matsuki, Tohru; Matthews, Russell T; Cooper, Jonathan A et al. (2010) Reelin and stk25 have opposing roles in neuronal polarization and dendritic Golgi deployment. Cell 143:826-36
Simo, Sergi; Jossin, Yves; Cooper, Jonathan A (2010) Cullin 5 regulates cortical layering by modulating the speed and duration of Dab1-dependent neuronal migration. J Neurosci 30:5668-76
Laszlo, George S; Cooper, Jonathan A (2009) Restriction of Src activity by Cullin-5. Curr Biol 19:157-62
Feng, Libing; Cooper, Jonathan A (2009) Dual functions of Dab1 during brain development. Mol Cell Biol 29:324-32

Showing the most recent 10 out of 50 publications