Protein O-GlcNAcylation: emerging mechanisms and functions

X Yang, K Qian - Nature reviews Molecular cell biology, 2017 - nature.com
Nature reviews Molecular cell biology, 2017nature.com
O-GlcNAcylation—the attachment of O-linked N-acetylglucosamine (O-GlcNAc) moieties to
cytoplasmic, nuclear and mitochondrial proteins—is a post-translational modification that
regulates fundamental cellular processes in metazoans. A single pair of enzymes—O-
GlcNAc transferase (OGT) and O-GlcNAcase (OGA)—controls the dynamic cycling of this
protein modification in a nutrient-and stress-responsive manner. Recent years have seen
remarkable advances in our understanding of O-GlcNAcylation at levels that range from …
Abstract
O-GlcNAcylation — the attachment of O-linked N-acetylglucosamine (O-GlcNAc) moieties to cytoplasmic, nuclear and mitochondrial proteins — is a post-translational modification that regulates fundamental cellular processes in metazoans. A single pair of enzymes — O-GlcNAc transferase (OGT) and O-GlcNAcase (OGA) — controls the dynamic cycling of this protein modification in a nutrient- and stress-responsive manner. Recent years have seen remarkable advances in our understanding of O-GlcNAcylation at levels that range from structural and molecular biology to cell signalling and gene regulation to physiology and disease. New mechanisms and functions of O-GlcNAcylation that are emerging from these recent developments enable us to begin constructing a unified conceptual framework through which the significance of this modification in cellular and organismal physiology can be understood.
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