MYC is a transcription factor that targets a large fraction (~15%) of the genome and is tightly regulated in normal cells and essential for normal development and homeostasis in most animals. Deregulated MYC expression (e.g., overexpression) is tumorigenic in mice and associated with most types of cancer in humans. MYC deregulation may occur via alterations of the c-myc gene itself (e.g., translocation and amplification) or via aberrant activation of upstream signaling pathways that activate c-myc gene expression and/or increase MYC protein stability via post-translational modifications (PTMs). The PTMs of MYC are, however, poorly characterized and their roles in the multiple cellular and molecular activities of MYC are still poorly defined and controversial. Until recently phosphorylation and O-glycosylation of a few residues were the only PTMs reported, which affect MYC ubiqitination and degradation by the proteasome. Our lab recently uncovered novel PTMs of MYC and found that MYC is acetylated at several lysine (K) residues by transcription coactivators with histone acetyltransferase (HAT) activity (i.e., GCN5 and p300). The general objective of my research is to provide definitive evidence that native MYC in mammalian cells is regulated via acetylation and to define the cellular and molecular functions of MYC acetylation at specific residues.
AIM 1 : To establish and characterize acetylation of native MYC in mammalian cells using acetylated site-specific antibodies (MYC-K148Ac, MYC-K157Ac, MYC-K323Ac) Acetylation of endogenous MYC has yet to be demonstrated in any cell type. I will use new antibodies that recognize specifically human MYC acetylated residues K148, K157, and K323 to profile acetylation of MYC at these different sites in several non-transformed and transformed/cancer cell lines.
AIM 2 : To identify functions of MYC acetylated residues K148(149) and K157(158) I will test the role of MYC acetylated residues K148 and K157 (human coordinates homologous to mouse MYC K149 and K158) in MYC-induced cell proliferation, transformation and apoptosis.
AIM 3 : To establish and define the role(s) of MYC acetylation in target gene regulation Selected MYC target genes affected by the R158 (or R149) substitution identified in preliminary experiments (e.g. Nrf1) and in Aim 2 will be analyzed to tes the possible role of acetylation at K158 (or K149) in regulating MYC transcription functions. Various methods, including chromatin immunoprecipitation (ChIP) assays, RNA interference (RNAi), and reporter gene assays will be used.

Public Health Relevance

The MYC family proteins are tightly regulated in normal cells by growth and mitogenic factors, by differentiation and developmental stimuli, and by cellular stress signals;however, in most cancers MYC expression is deregulated leading to its constitutive (e.g. growth factor- independent) expression and often overexpression in advanced/aggressive tumors. Given the successful outcome of my research I purpose the following health related advancements: identification of novel biomarkers for specific cell states (i.e. cell death), and the discovery of possible interventions to selectively inhibit cellular transformation but not apoptosis (cancer drug therapies).

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Predoctoral Individual National Research Service Award (F31)
Project #
5F31CA165776-04
Application #
8717607
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Vallejo-Estrada, Yolanda
Project Start
2011-09-01
Project End
2016-08-31
Budget Start
2014-09-01
Budget End
2015-08-31
Support Year
4
Fiscal Year
2014
Total Cost
Indirect Cost
Name
University of California Riverside
Department
Biochemistry
Type
Earth Sciences/Resources
DUNS #
City
Riverside
State
CA
Country
United States
Zip Code
92521