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Bittersweet memories: linking metabolism to epigenetics through O-GlcNAcylation
被引:333
作者:
Hanover, John A.
[1
]
Krause, Michael W.
[2
]
Love, Dona C.
[1
]
机构:
[1] NIDDK, Lab Cell & Mol Biol, NIH, Bethesda, MD 20892 USA
[2] NIDDK, Mol Biol Lab, NIH, Bethesda, MD USA
关键词:
EMBRYONIC STEM-CELLS;
LINKED GLCNAC TRANSFERASE;
BETA-N-ACETYLGLUCOSAMINIDASE;
THRIFTY PHENOTYPE HYPOTHESIS;
POLYCOMB GROUP GENES;
INSULIN-RESISTANCE;
CAENORHABDITIS-ELEGANS;
TETRATRICOPEPTIDE REPEATS;
DROSOPHILA-MELANOGASTER;
PROTEIN GLYCOSYLATION;
D O I:
10.1038/nrm3334
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
O-GlcNAcylation, which is a nutrient-sensitive sugar modification, participates in the epigenetic regulation of gene expression. The enzymes involved in O-linked beta-D-N-acetylglucosamine (O-GlcNAc) cycling - O-GlcNAc transferase (OGT) and O-GlcNAcase (OGA) - target key transcriptional and epigenetic regulators including RNA polymerase II, histones, histone deacetylase complexes and members of the Polycomb and Trithorax groups. Thus, O-GlcNAc cycling may serve as a homeostatic mechanism linking nutrient availability to higher-order chromatin organization. In response to nutrient availability, O-GlcNAcylation is poised to influence X chromosome inactivation and genetic imprinting, as well as embryonic development. The wide range of physiological functions regulated by O-GlcNAc cycling suggests an unexplored nexus between epigenetic regulation in disease and nutrient availability.
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页码:312 / 321
页数:10
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