| Literature DB >> 27497832 |
Willayat Y Wani1, John C Chatham1, Victor Darley-Usmar1, Lori L McMahon2, Jianhua Zhang3.
Abstract
O-GlcNAcylation is a dynamic form of protein glycosylation which involves the addition of β-d-N-acetylglucosamine (GlcNAc) via an O-linkage to serine or threonine residues of nuclear, cytoplasmic, mitochondrial and transmembrane proteins. The two enzymes responsible for O-GlcNAc cycling are O-GlcNAc transferase (OGT) and O-GlcNAcase (OGA); their expression and activities in brain are age dependent. More than 1000 O-GlcNAc protein targets have been identified which play critical roles in many cellular processes. In mammalian brain, O-GlcNAc modification of Tau decreases its phosphorylation and toxicity, suggesting a neuroprotective role of pharmacological elevation of brain O-GlcNAc for Alzheimer's disease treatment. Other observations suggest that elevating O-GlcNAc levels may decrease protein clearance or induce apoptosis. This review highlights some of the key findings regarding O-GlcNAcylation in models of neurodegenerative diseases.Entities:
Keywords: Aging; Amyloid; Autophagy; Huntingtin; OGA; OGT; Synuclein; Tau
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Year: 2016 PMID: 27497832 PMCID: PMC5292095 DOI: 10.1016/j.brainresbull.2016.08.002
Source DB: PubMed Journal: Brain Res Bull ISSN: 0361-9230 Impact factor: 4.077