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Degrees: 1999 - PhD - Stanford University - Biochemistry 1993 - BA - Harvard University - Biochemistry Awards: Helen Hay Whitney Fellowship Alfred P. Sloan Research Fellowship Department and Center Affiliations: Center for Neuroscience Genome Center Cancer Center Professional Societies: American Society of Cell Biology Society for Neuroscience Grad Group Affiliations and Specialties: Biochemistry and Molecular Biology Cell and Developmental Biology Neuroscience Non-DBS Grad Group(s) - Pharmacology & Toxicology Publications: Yun JS, Rust JM, Ishimaru T, and DÃaz E (2007), A novel role for the Mad family member Mad3 in cerebellar granule neuron precursor proliferation, Mol. Cell. Biol. 27: 8178-8189. Barisone GA, Yun JS, and DÃaz E (2008), From cellellar proliferation to tumorigenesis: novel insights into the role of Mad3 [invited Extra-View], Cell Cycle, in press. DÃaz E (2006), A functional genomics guide to the galaxy of neuronal cell types [News & Views article]. Nat. Neurosci. 9: 10-12. Diaz E, Ge Y, Yang YH, Loh KC, Serafini TA, Okazaki Y, Hayashizaki Y, Speed TP, Ngai J and Scheiffele P. (2002). Molecular analysis of gene expression in the developing pontocerebellar projection system. Neuron 36, 417-434. Diaz E, Yang YH, Ferreira T, Loh KC, Okazaki Y, Hayashizaki Y, Tessier-Lavigne M, Speed TP and Ngai J (2003). Analysis of gene expression in the developing mouse retina, Proc. Natl. Acad. Sci. USA 100, 5491-5496. Diaz E and Pfeffer SR (1998). TIP47: A cargo selection device for mannose 6-phosphate receptor trafficking. Cell 93, 433-443. Diaz E, Schimmoller F and Pfeffer SR (1997). A novel Rab9 effector required for endosome-to-TGN transport. J. Cell Biol. 138, 283-290. Research Interests: FUNCTIONAL GENOMICS OF NERVOUS SYSTEM DEVELOPMENT: My lab's main research interest is to understand molecular mechanisms of neural development using a rodent model system. In particular, my lab is interested in two areas: neural proliferation and synapse development. We used DNA microarrays as a tool to identify genes that are developmentally regulated during postnatal cerebellum development. We have identified several candidate molecules that increase in gene expression during the period of neural proliferation or synapse formation and we are currently studying the role of two molecules (Mad3 and synDIG1) in these processes. MAD3 AND NEURAL PROLIFERATION: During development, Sonic hedgehog (Shh) regulates the proliferation of cerebellar granule neuron precursors (GNPs) in part via expression of Nmyc. My lab has demonstrated a novel role for the Myc/Max/Mad family member Mad3 in the Shh pathway to regulate Nmyc expression and cerebellar GNP proliferation. Mad3 mRNA is transiently expressed in GNPs during proliferation. Cultured GNPs express Mad3 in response to Shh stimulation in a cyclopamine-dependent manner. Mad3 is necessary for Shh-dependent GNP proliferation as measure by BrdU incorporation and Nmyc expression. Furthermore, overexpression of Mad3, but not other Mad proteins, is sufficient to induce GNP proliferation in the absence of Shh. Interestingly, cerebellar tumors and pre-tumor cells derived from patched (ptc) heterozygous mices express high levels of Mad3 compared with adjacent normal cerebellar tissue. These studies support a novel role for Mad3 in cerebellar GNP proliferation, and possibly tumorigenesis, and challenge the current paradigm that Mad3 should antagonize Nmyc by competition for direct DNA binding via Max dimerization. Our current research aims are: 1) to identify Mad3 target genes in GNPs and tumor cells using chromatin immunoprecipitation (ChIP) coupled to DNA microarrays (ChIP-on-chip); 2) to identify Mad3 interacting proteins using biochemical, genetic and proteomic approaches; and 3) to understand the role of Mad3 in tumor formation using in vivo mouse models. SYNDIG1 AND SYNAPSE DEVELOPMENT: During development, synapse formation relies on signaling between pre- and postsynaptic neurons and the expression of specific genes. Synapse Differentiation Induced Gene (synDIG1) was identified as a gene upregulated during synapse development whose upregulation failed in a mutant mouse line with defects in synaptic differentiation. We have shown that synDIG1 encodes a novel, postsynaptic transmembrane protein that is a critical regulator of synapse development in cultured hippocampal neurons. Interestingly, synDIG defines a family of four genes within the mouse genome that are expressed in distinct and partially overlapping cell types within nervous sytem tissues. Intriguingly, overexpression or knock-down of synDIG1 in cultured neurons alters the electrophysiological properties of excitatory synaptic transmission, presumably by the altered trafficking of AMPA receptors. Our current research aims are: 1) to generate and characterize mice with a conditional deletion of the synDIG1 gene; 2) to identify synDIG1-interacting proteins; and 3) to test if synDIG1 is subject to activity-dependent regulation at synapses. http://www.ucdmc.ucdavis.edu/pharmacology/departmentlabs/diazlab.html Laboratory Personnel: 3409A Genome & Biomedical Sciences Facility - Jun-Soo Yun (Grad student, CDB); Evgenia Kalashnikova (Grad student, BMB); Sameen Azizi (Jr. Specialist I); Gustavo Barisone (Postdoc); Inderpreet Kaur (Jr. Specialist I); Van La (Undergrad student, BioSci); Wanna Matayasuwan (Undergrad student, BioSci); Martin Tran (Research Assistant II); Melissa Aguayo (Undergrad student, BioSci). http://www.ucdmc.ucdavis.edu/pharmacology/departmentlabs/diazlab.html Teaching Interests:Developmental neurobiology, cell biology of the neuron, genomics Courses Taught: NSC 224A Molecular and Developmental Neuroscience - Term(s): Winter NSC 298 Cell Biology of the Neuron Journal Club - Term(s): Winter,Spring |
![[Picture of Elva Diaz]](/FacultyProfiles/Common/PersonalImages/1817.jpg)