GNE protein expression and subcellular distribution are unaltered in HIBM.

Abstract

Mutations in GNE encoding UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase (GNE) cause hereditary inclusion body myopathy (HIBM). To define the role of GNE mutations in HIBM pathogenesis, GNE protein expression was analyzed. GNE protein is expressed at equal levels in HIBM patients and normal control subjects. Immunofluorescence detection of GNE did not reveal any mislocalization of GNE in skeletal muscle. We conclude that impaired GNE function, not lack of expression, may be the key pathogenic factor in HIBM. For diagnostic purposes, direct genetic analysis of the GNE gene in patients with IBM will remain the mainstay and is not aided by immunohistochemistry or immunoblotting using antibodies against the GNE protein.

• Authors: S Krause, A Aleo, S Hinderlich, L Merlini, I Tournev, M C Walter, Z Argov, S Mitrani-Rosenbaum, H Lochmüller
• Journal: Neurology (Neurology) Vol. 69 Issue 7 Pg. 655-9 (Aug 14 2007) ISSN: 1526-632X [Electronic] United States
• PMID: 17698786 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Multienzyme Complexes
• UDP-N-acetylglucosamine 2-epimerase - N-acetylmannosamine kinase
• Phosphotransferases (Alcohol Group Acceptor)
• N-acylmannosamine kinase
• Carbohydrate Epimerases
• UDP acetylglucosamine-2-epimerase

Topics

• Adult
• Carbohydrate Epimerases (biosynthesis, genetics)
• Cell Line
• Female
• Gene Expression Regulation, Enzymologic
• Humans
• Male
• Multienzyme Complexes (biosynthesis, genetics)
• Mutation
• Myositis, Inclusion Body (enzymology, genetics)
• Phosphotransferases (Alcohol Group Acceptor) (biosynthesis, genetics)
• Subcellular Fractions (enzymology)