O-GlcNAc transferase (OGT), found in all metazoans, is essential for embryonic development in mammals and continues to be required throughout life for the viability of proliferating cells. Although the importance of OGT in biology is not disputed its functions remain poorly understood. It has three distinct biochemical activities: 1) it acts asa glycosyltransferase, attaching N-acetylglucosamine (GlcNAc) to a wide variety of cytoplasmic and nuclear proteins and thereby affecting their stability, localization, and biochemical functions in response to changing cellular conditions; 2) it functions as a protease in the maturation of HCF-1, an essential multi-domain transcriptional co-regulator required for cell cycle progression; and 3) it serves as a scaffolding protein that interacts with components of several multi-protein complexes. OGT has been implicated in diseases involving dysregulated glucose uptake and metabolism, including cancer and diabetes, and it is a proposed therapeutic target. The research proposed here combines chemical synthesis, biochemistry, and cell biology to gain a better understanding of OGT's different activities, which is critical for assessing its potential a a therapeutic target.
Aim 1 focuses on the development of cell permeable small molecule inhibitors based on a lead discovered in the previous funding period. These inhibitors will be useful for investigating OGT's cellular activities and are particularly important for studies of it roles in cell signaling.
Aim 2 focuses on using protein microarrays to investigate the structural features of OGT that are important for substrate selection. These studies may reveal that different parts of the OGT TPR domain are involved in selecting different subsets of substrates, a result that would have implications for pathway-selective OGT inhibitors.
Aim 3 focuses on testing our proposed mechanism for how OGT cleaves HCF-1. These studies are warranted because the mechanism, like the discovery that OGT uses the same active site for both protein O-GlcNAcylation and proteolysis, is unprecedented in biology. Finally, Aim 4 focuses on establishing a genetic system to replace wildtype OGT with OGT variants deficient in a particular biochemical activity so that we can address the following fundamental questions: Why is OGT required for survival of proliferating mammalian cells? Is HCF-1 cleavage required? Is OGT's scaffolding function required? Or is O-GlcNAcylation activity necessary, and, if so, what targets are most important? A robust genetic system to investigate OGT variants will allow us to link findings from biochemical studies to cellular phenotypes, leading to a better understanding of OGT biology.

Public Health Relevance

Nutrient-sensing pathways are commonly deregulated in human diseases, including diabetes and cancer. O- GlcNAc transferase (OGT) has been implicated in glucose-sensing and stress response pathways, and is a proposed therapeutic target for cancer. The work in this grant will provide new insights into the chemistry and biology of OGT, and may lead to small molecule inhibitors useful for testing OGT's potential as an anticancer target.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM094263-07
Application #
9427993
Study Section
Synthetic and Biological Chemistry A Study Section (SBCA)
Program Officer
Marino, Pamela
Project Start
2012-02-01
Project End
2020-02-29
Budget Start
2018-03-01
Budget End
2019-02-28
Support Year
7
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Harvard Medical School
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
047006379
City
Boston
State
MA
Country
United States
Zip Code
02115
Janetzko, John; Walker, Suzanne (2017) Aspartate Glycosylation Triggers Isomerization to Isoaspartate. J Am Chem Soc 139:3332-3335
Janetzko, John; Trauger, Sunia A; Lazarus, Michael B et al. (2016) How the glycosyltransferase OGT catalyzes amide bond cleavage. Nat Chem Biol 12:899-901
Itkonen, Harri M; Gorad, Saurabh S; Duveau, Damien Y et al. (2016) Inhibition of O-GlcNAc transferase activity reprograms prostate cancer cell metabolism. Oncotarget 7:12464-76
Levine, Zebulon G; Walker, Suzanne (2016) The Biochemistry of O-GlcNAc Transferase: Which Functions Make It Essential in Mammalian Cells? Annu Rev Biochem 85:631-57
Angelova, Magdalena; Ortiz-Meoz, Rodrigo F; Walker, Suzanne et al. (2015) Inhibition of O-Linked N-Acetylglucosamine Transferase Reduces Replication of Herpes Simplex Virus and Human Cytomegalovirus. J Virol 89:8474-83
Ortiz-Meoz, Rodrigo F; Jiang, Jiaoyang; Lazarus, Michael B et al. (2015) A small molecule that inhibits OGT activity in cells. ACS Chem Biol 10:1392-7
Ortiz-Meoz, Rodrigo F; Merbl, Yifat; Kirschner, Marc W et al. (2014) Microarray discovery of new OGT substrates: the medulloblastoma oncogene OTX2 is O-GlcNAcylated. J Am Chem Soc 136:4845-8
Sherman, David J; Lazarus, Michael B; Murphy, Lea et al. (2014) Decoupling catalytic activity from biological function of the ATPase that powers lipopolysaccharide transport. Proc Natl Acad Sci U S A 111:4982-7
Janetzko, John; Walker, Suzanne (2014) The making of a sweet modification: structure and function of O-GlcNAc transferase. J Biol Chem 289:34424-32
Lazarus, Michael B; Jiang, Jiaoyang; Kapuria, Vaibhav et al. (2013) HCF-1 is cleaved in the active site of O-GlcNAc transferase. Science 342:1235-9

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