McArdle's disease: biochemical and molecular genetic studies.

TitleMcArdle's disease: biochemical and molecular genetic studies.
Publication TypeJournal Article
Year of Publication1988
AuthorsServidei, S, Shanske, S, Zeviani, M, Lebo, R, Fletterick, R, DiMauro, S
JournalAnn Neurol
Volume24
Issue6
Pagination774-81
Date Published1988 Dec
ISSN0364-5134
KeywordsBiopsy, Blotting, Northern, DNA Probes, Electrophoresis, Polyacrylamide Gel, Enzyme-Linked Immunosorbent Assay, Female, Glycogen Storage Disease Type V, Humans, Immunoblotting, Male, Muscles, Phosphorylases, RNA, Messenger
Abstract

We have analyzed muscle biopsy specimens from 48 patients with biochemically proven phosphorylase deficiency (McArdle's disease) by sodium dodecylsulphate polyacrylamide gel electrophoresis (SDS-PAGE), immunoblotting, and immunotitration (enzyme-linked immunosorbent assay [ELISA]). Thirty-five of the 42 patients studied by SDS-PAGE and immunoblot, and 41 of the 48 patients studied by ELISA had no detectable enzyme protein. Six patients had markedly decreased phosphorylase protein by all three assays, and only 1 patient had a normal amount of protein. No apparent correlation existed between the presence or absence of enzyme protein and the clinical presentation or muscle glycogen concentration. Northern analysis was performed on muscle RNA in 4 patients: messenger RNA was normal in 2, abnormally short in 1, and absent in the fourth, indicating heterogeneity of the molecular lesion in McArdle's disease.

DOI10.1002/ana.410240612
Alternate JournalAnn. Neurol.
Citation Key10.1002/ana.410240612
PubMed ID3207360
Grant ListNS 11766 / NS / NINDS NIH HHS / United States