Modification of nuclear and cytoplasmic proteins by O-linked N-acetylglucosamine (O-GlcNAc) is as abundant and as dynamic as protein phosphorylation in all metazoans. The dynamic interplay between O-GlcNAc and O-phosphate plays a key role cellular signaling, transcription and in the functions of nuclear oncogene and tumor suppressor proteins. O-GlcNAc also plays a key role in protecting cells from varied forms of stress, suggesting that the saccharide is important to tumor cell survival mechanisms. Our long-term goal is to elucidate the functions and interplay between O-GlcNAc and O-phosphate important to the oncogenic and metastatic phenotype. This application builds upon years of methods development to directly determine the molecular roles of O-GlcNAc on c-Myc oncogene protein, Rb tumor suppressors and in the cellular mechanisms protecting cells from extreme stresses.
Specific Aims are:
Aim 1 : Elucidate the functions of O-GIcNAc On the c-Myc oneogene protein. A. Quantify the dynamic modification of c-Myc's transactivation domain (TAD) as a function of growth, cellcycle, apoptosis, & stress using CE-laser flourecence-MS/MS. B. Determine the functions of c-Myc TAD isoforms using mutant c-Myc and intein-produced isoforms. C. In vitro physical analyses of the structures of c-Myc TAD isoforms. D. Comparative kinetic analyses of O-GlcNAc Transferase, GSK3( and MAP kinases on glyco/phospho forms of the c-Myc TAD region.
Aim 2 : Determine the functions of O-GIcNAc on the tumor suppressor Rb and Rb p107 proteins. A. Map O-GlcNAc Sites. B. Quantify changes in OGlcNAc/O-phosphate during cell-cycle, cell growth and apoptosis. C. Comparative analyses of Rb & p107 isoforms protein:protein interactions and transcriptional activities.
Aim 3 : Determine the roles of O-GIcNAc in protecting cells from stress. A. Mechanisms upregulating O-GlcNAc in response to stress. B. Functions of O-GlcNAc on HSP70. C. Elevated O-GlcNAc affects on apoptosis and protein aggregation? These studies are elucidating molecular mechanisms of oncogenesis and metastasis, over-looked by others, that could lead to unexpected therapeutic approaches.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA042486-22
Application #
6862770
Study Section
Physiological Chemistry Study Section (PC)
Program Officer
Sussman, Daniel J
Project Start
1986-05-01
Project End
2009-02-28
Budget Start
2005-03-01
Budget End
2006-02-28
Support Year
22
Fiscal Year
2005
Total Cost
$367,875
Indirect Cost
Name
Johns Hopkins University
Department
Biochemistry
Type
Schools of Medicine
DUNS #
001910777
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Ma, Junfeng; Hart, Gerald W (2017) Analysis of Protein O-GlcNAcylation by Mass Spectrometry. Curr Protoc Protein Sci 87:24.10.1-24.10.16
Bullen, John W; Balsbaugh, Jeremy L; Chanda, Dipanjan et al. (2014) Cross-talk between two essential nutrient-sensitive enzymes: O-GlcNAc transferase (OGT) and AMP-activated protein kinase (AMPK). J Biol Chem 289:10592-606
Hardivillé, Stéphan; Hart, Gerald W (2014) Nutrient regulation of signaling, transcription, and cell physiology by O-GlcNAcylation. Cell Metab 20:208-13
Copeland, Ronald J; Han, Guanghui; Hart, Gerald W (2013) O-GlcNAcomics--Revealing roles of O-GlcNAcylation in disease mechanisms and development of potential diagnostics. Proteomics Clin Appl 7:597-606
Hart, Gerald W (2013) Nutrient regulation of immunity: O-GlcNAcylation regulates stimulus-specific NF-?B-dependent transcription. Sci Signal 6:pe26
Hart, Gerald W (2013) How sugar tunes your clock. Cell Metab 17:155-6
Ma, Junfeng; Hart, Gerald W (2013) Protein O-GlcNAcylation in diabetes and diabetic complications. Expert Rev Proteomics 10:365-80
Banerjee, Partha S; Hart, Gerald W; Cho, Jin Won (2013) Chemical approaches to study O-GlcNAcylation. Chem Soc Rev 42:4345-57
Alfaro, Joshua F; Gong, Cheng-Xin; Monroe, Matthew E et al. (2012) Tandem mass spectrometry identifies many mouse brain O-GlcNAcylated proteins including EGF domain-specific O-GlcNAc transferase targets. Proc Natl Acad Sci U S A 109:7280-5
Tarrant, Mary Katherine; Rho, Hee-Sool; Xie, Zhi et al. (2012) Regulation of CK2 by phosphorylation and O-GlcNAcylation revealed by semisynthesis. Nat Chem Biol 8:262-9

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