beta-N-Acetylglucosamine (O-GlcNAc) is a regulatory post-translational modification of nuclear and cytosolic proteins. The enzymes for its addition and removal have recently been cloned and partially characterized. While only about 80 mammalian proteins have been identified to date that carry this modification, it is clear that this represents just a small percentage of the modified proteins. O-GlcNAc has all the properties of a regulatory modification including being dynamic and inducible. The modification appears to modulate transcriptional and signal transduction events. There are also accruing data that O-GlcNAc plays a role in apoptosis and neurodegeneration. A working model is emerging that O-GlcNAc serves as a metabolic sensor that attenuates a cell's response to extracellular stimuli based on the energy state of the cell. In this review, we will focus on the enzymes that add/remove O-GlcNAc, the functional impact of O-GlcNAc modification, and the current working model for O-GlcNAc as a nutrient sensor. (C) 2003 Published by Elsevier Science (USA).
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Department of Anatomy, Kyorin University, School of Medicine, MitakaDepartment of Anatomy, Kyorin University, School of Medicine, Mitaka
Akimoto Y.
Hart G.W.
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Department of Biological Chemistry, Johns Hopkins School of Medicine, Baltimore, MDDepartment of Anatomy, Kyorin University, School of Medicine, Mitaka
Hart G.W.
Hirano H.
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Department of Anatomy, Kyorin University, School of Medicine, Mitaka
Nittai Jusei Medical College for Judo Therapeutics, TokyoDepartment of Anatomy, Kyorin University, School of Medicine, Mitaka
Hirano H.
Kawakami H.
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Department of Anatomy, Kyorin University, School of Medicine, MitakaDepartment of Anatomy, Kyorin University, School of Medicine, Mitaka