Aberrant O-GlcNAcylation disrupts GNE enzyme activity in GNE myopathy.

Abstract

UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase (GNE) is the key enzyme for the biosynthesis of sialic acids. Sialic acids are terminal monosaccharides of glycoconjugates and gangliosides, which have an essential influence on various cell interactions. The sialylation of proteins varies during development, aging, and pathogenesis of degenerative diseases such as Morbus Alzheimer, diabetes mellitus type II, or myopathies. Mutation of methionine 743 in the GNE leads to a 30% reduction of the enzyme activity and is responsible for an aggressive form of GNE myopathy. GNE myopathy or hereditary inclusion body myopathy (HIBM) is an age-dependent muscular dystrophy. Here, we analyzed the impact of the exchange of methionine to threonine at position 743 which introduces an additional potential phosphorylation/O-GlcNAcylation site. We found increased O-GlcNAcylation of the M743T variant compared to the wild-type GNE. In addition, removal of the O-GlcNAc of the M743T variant resulted in an increased activity comparable to activity of the wild-type GNE. Furthermore, the half-life of the M743T variant is two times longer than for the wild-type GNE protein. This study provides that the balance of phosphorylation and O-GlcNAcylation is decisive involved in efficiency and regulation of GNE.

• Authors: Dorit Bennmann, Wenke Weidemann, Annett Thate, Denise Kreuzmann, Rüdiger Horstkorte
• Journal: The FEBS journal (FEBS J) Vol. 283 Issue 12 Pg. 2285-94 (06 2016) ISSN: 1742-4658 [Electronic] England
• PMID: 27037841 (Publication Type: Journal Article)
• Copyright: © 2016 Federation of European Biochemical Societies.

Chemical References

• Multienzyme Complexes
• Sialic Acids
• UDP-N-acetylglucosamine 2-epimerase - N-acetylmannosamine kinase
• Methionine
• Acetylglucosamine

Topics

• Acetylglucosamine (metabolism)
• Acylation (genetics)
• Distal Myopathies (genetics, metabolism, pathology)
• Genotype
• HeLa Cells
• Humans
• Methionine (genetics)
• Multienzyme Complexes (genetics, metabolism)
• Muscular Dystrophies (genetics, metabolism, pathology)
• Mutation
• Phosphorylation
• Plasmids (genetics)
• Sialic Acids (biosynthesis, genetics)