Author:
Konzman Daniel,Abramowitz Lara K.,Steenackers Agata,Mukherjee Mana Mohan,Na Hyun-Jin,Hanover John A.
Abstract
Cellular identity in multicellular organisms is maintained by characteristic transcriptional networks, nutrient consumption, energy production and metabolite utilization. Integrating these cell-specific programs are epigenetic modifiers, whose activity is often dependent on nutrients and their metabolites to function as substrates and co-factors. Emerging data has highlighted the role of the nutrient-sensing enzymeO-GlcNAc transferase (OGT) as an epigenetic modifier essential in coordinating cellular transcriptional programs and metabolic homeostasis. OGT utilizes the end-product of the hexosamine biosynthetic pathway to modify proteins withO-linked β-D-N-acetylglucosamine (O-GlcNAc). The levels of the modification are held in check by theO-GlcNAcase (OGA). Studies from model organisms and human disease underscore the conserved function these two enzymes ofO-GlcNAc cycling play in transcriptional regulation, cellular plasticity and mitochondrial reprogramming. Here, we review these findings and present an integrated view of howO-GlcNAc cycling may contribute to cellular memory and transgenerational inheritance of responses to parental stress. We focus on a rare human genetic disorder where mutant forms of OGT are inherited or acquiredde novo. Ongoing analysis of this disorder, OGT- X-linked intellectual disability (OGT-XLID), provides a window into how epigenetic factors linked toO-GlcNAc cycling may influence neurodevelopment.
Subject
Genetics(clinical),Genetics,Molecular Medicine
Cited by
19 articles.
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