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Metabolic inhibitors of O-GlcNAc transferase (OGT) that act in vivo implicate decreased O-GlcNAc levels in leptin-mediated nutrient sensing

Research output: Contribution to journalArticle

Author(s)

Ta-wei Liu, Wesley F. Zandberg, Tracey M. Gloster, Lehua Deng, Kelsey D Murray, Xiaoyang Shan, David Jaro Vocadlo

School/Research organisations

Abstract

O‐linked glycosylation of serine and threonine residues of nucleocytoplasmic proteins with N‐acetylglucosamine (O‐GlcNAc) residues is catalyzed by O‐GlcNAc transferase (OGT). O‐GlcNAc is conserved within mammals and is implicated in a wide range of physiological processes. Here we describe metabolic precursor inhibitors of OGT suitable for use both in cells and in vivo in mice. These 5‐thiosugar analogues of N‐acetylglucosamine are assimilated through a convergent metabolic pathway, most likely involving N‐acetylglucosamine‐6‐phosphate de‐N‐acetylase (NAGA) to generate a common OGT inhibitor within cells. Of these inhibitors, we show that 2‐deoxy‐2‐N‐hexanamide‐5‐thio‐D‐glucopyranoside (5SGlcNHex) acts in vivo to induce dose‐ and time‐dependent decreases in O‐GlcNAc levels in various tissues. Decreased O‐GlcNAc correlates, both in vitro within adipocytes and in vivo within mice, with lower levels of transcription factor Sp1 and the satiety‐inducing hormone leptin ‐ revealing a link between decreased O‐GlcNAc levels and nutrient sensing in peripheral tissues of mammals.
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Original languageEnglish
Pages (from-to)7644-7648
JournalAngewandte Chemie International Edition
Volume57
Issue number26
Early online date24 May 2018
DOIs
Publication statusPublished - 25 Jun 2018

    Research areas

  • Glycoprotein, Thiosugar, Nucleotide sugars, Leptin, Nutrient sensing

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