A little sugar goes a long way: The cell biology of O-GlcNAc

被引:450
作者
Bond, Michelle R.
Hanover, John A.
机构
关键词
LINKED N-ACETYLGLUCOSAMINE; NUCLEAR-PORE COMPLEX; RNA-POLYMERASE-II; ACTIVATED PROTEIN-KINASE; NITRIC-OXIDE SYNTHASE; TRANSFERASE OGT; CYTOSOLIC PROTEINS; INSULIN-RESISTANCE; TERMINAL DOMAIN; BETA-CATENIN;
D O I
10.1083/jcb.201501101
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Unlike the complex glycans decorating the cell surface, the O-linked. beta-N-acetyl glucosamine (O-GlcNAc) modification is a simple intracellular Ser/Thr-linked monosaccharide that is important for disease-relevant signaling and enzyme regulation. O-GlcNAcylation requires uridine diphosphate-GlcNAc, a precursor responsive to nutrient status and other environmental cues. Alternative splicing of the genes encoding the O-GlcNAc cycling enzymes O-GlcNAc transferase (OGT) and O-GlcNAcase (OGA) yields isoforms targeted to discrete sites in the nucleus, cytoplasm, and mitochondria. OGT and OGA also partner with cellular effectors and act in tandem with other posttranslational modifications. The enzymes of O-GlcNAc cycling act preferentially on intrinsically disordered domains of target proteins impacting transcription, metabolism, apoptosis, organelle biogenesis, and transport.
引用
收藏
页码:869 / 880
页数:12
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