| Literature DB >> 8702726 |
B F Smith1, H Stedman, Y Rajpurohit, P S Henthorn, J H Wolfe, D F Patterson, U Giger.
Abstract
Muscle type phosphofructokinase (M-PFK) deficiency is a rare inherited glycogen storage disease in humans that causes exertional myopathy and hemolysis. The molecular basis of canine M-PFK deficiency, the only naturally occurring animal homologue, was investigated. Lack of M-PFK enzyme activity was caused by a nonsense mutation in the penultimate exon of the M-PFK gene, leading to rapid degradation of a truncated (40 amino acids) and therefore unstable M-PFK protein. A polymerase chain reaction-based test was devised to identify M-PFK-deficient and carrier animals. This represents one of only a few inborn errors of metabolism where the molecular defect has been identified in a large animal model which can now be used to develop and assess novel therapeutic strategies.Entities:
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Year: 1996 PMID: 8702726 DOI: 10.1074/jbc.271.33.20070
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157