O‐GlcNAc turns twenty: functional implications for post‐translational modification of nuclear and cytosolic proteins with a sugar
- 11 June 2003
- journal article
- review article
- Published by Wiley in FEBS Letters
- Vol. 546 (1) , 154-158
- https://doi.org/10.1016/s0014-5793(03)00641-0
Abstract
O-linked beta-N-acetylglucosamine (O-GlcNAc) is a dynamic nucleocytoplasmic post-translational modification more analogous to phosphorylation than to classical complex O-glycosylation. A large number of nuclear and cytosolic proteins are modified by O-GlcNAc. Proteins modified by O-GlcNAc include transcription factors, signaling components, and metabolic enzymes. While the modification has been known for almost 20 years, functions for the monosaccharide modification are just now emerging. In this review, we will focus on the cycling enzymes and emerging roles for this post-translational modification in regulating signal transduction and transcription. Finally, we will discuss future directions and the working model of O-GlcNAc serving as a nutrient sensor.Keywords
This publication has 46 references indexed in Scilit:
- Insulin Resistance of Glycogen Synthase Mediated byO-Linked N-AcetylglucosamineJournal of Biological Chemistry, 2003
- Mitochondrial and nucleocytoplasmic targeting of O-linked GlcNAc transferaseJournal of Cell Science, 2003
- Homology between O-linked GlcNAc transferases and proteins of the glycogen phosphorylase superfamily 1 1Edited by J. ThorntonJournal of Molecular Biology, 2001
- Glycan‐dependent signaling: O‐linked N‐acetylglucosamineThe FASEB Journal, 2001
- Functional Expression of O-linked GlcNAc TransferaseJournal of Biological Chemistry, 2000
- O-GlcNAc and the control of gene expressionBiochimica et Biophysica Acta (BBA) - General Subjects, 1999
- The tetratricopeptide repeat: a structural motif mediating protein-protein interactionsBioEssays, 1999
- O-Linked GlcNAc Transferase Is a Conserved Nucleocytoplasmic Protein Containing Tetratricopeptide RepeatsJournal of Biological Chemistry, 1997
- Selective Oxidative Modification and Affinity Cleavage of Pigeon Liver Malic Enzyme by the Cu2+-Ascorbate SystemJournal of Biological Chemistry, 1995
- The tissue distribution of hexosaminidase S and hexosaminidase CAnnals of Human Genetics, 1977