Abstract
Patients with McArdle's myopathy lack muscle glycogen phosphorylase (M-GP) activity. Regenerating and cultured muscle of patients with McArdle's myopathy presents a glycogen phosphorylase (GP) activity, but it is not firmly established whether M-GP or non-M-GP isoforms are expressed. We have cultured myoblasts from biopsy specimen of five patients with McArdle's myopathy. Skeletal muscle was cultured aneurally or was innervated by coculture with fetal rat spinal cord explants. In the patients' muscle biopsies and in their cultured innervated and aneural muscle we studied total GP activity, isoenzymatic pattern, reactivity with anti-M-GP antiserum, and presence of M-GP mRNA. There was no detectable enzymatic activity, no immunoreactivity with anti-M-GP antiserum, and no M-GP mRNA in the muscle biopsy of all patients. GP activity, M-GP isozyme, and anti-M-GP antiserum reactivity were present in patients' aneural cultures, increased after innervation, and were undistinguishable from control. M-GP mRNA was demonstrated in both aneural and innervated cultures of patients and control by primer extension and PCR amplification of total RNA. Our studies indicate that the M-GP gene is normally transcribed and translated in cultured muscle of patients with myophosphorylase deficiency.
Full text
PDFImages in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Askanas V., Engel W. K. A new program for investigating adult human skeletal muscle grown aneurally in tissue culture. Neurology. 1975 Jan;25(1):58–67. doi: 10.1212/wnl.25.1.58. [DOI] [PubMed] [Google Scholar]
- Askanas V., Gallez-Hawkins G. Synergistic influence of polypeptide growth factors on cultured human muscle. Arch Neurol. 1985 Aug;42(8):749–752. doi: 10.1001/archneur.1985.04210090013004. [DOI] [PubMed] [Google Scholar]
- Askanas V., Kwan H., Alvarez R. B., Engel W. K., Kobayashi T., Martinuzzi A., Hawkins E. F. De novo neuromuscular junction formation on human muscle fibres cultured in monolayer and innervated by foetal rat spinal cord: ultrastructural and ultrastructural--cytochemical studies. J Neurocytol. 1987 Aug;16(4):523–537. doi: 10.1007/BF01668506. [DOI] [PubMed] [Google Scholar]
- Burke J., Hwang P., Anderson L., Lebo R., Gorin F., Fletterick R. Intron/exon structure of the human gene for the muscle isozyme of glycogen phosphorylase. Proteins. 1987;2(3):177–187. doi: 10.1002/prot.340020303. [DOI] [PubMed] [Google Scholar]
- Cathala G., Savouret J. F., Mendez B., West B. L., Karin M., Martial J. A., Baxter J. D. A method for isolation of intact, translationally active ribonucleic acid. DNA. 1983;2(4):329–335. doi: 10.1089/dna.1983.2.329. [DOI] [PubMed] [Google Scholar]
- Chamberlain J. S., Gibbs R. A., Ranier J. E., Nguyen P. N., Caskey C. T. Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification. Nucleic Acids Res. 1988 Dec 9;16(23):11141–11156. doi: 10.1093/nar/16.23.11141. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Crerar M. M., Hudson J. W., Matthews K. E., David E. S., Golding G. B. Studies on the expression and evolution of the glycogen phosphorylase gene family in the rat. Genome. 1988 Aug;30(4):582–590. doi: 10.1139/g88-098. [DOI] [PubMed] [Google Scholar]
- David E. S., Crerar M. M. Quantitation of muscle glycogen phosphorylase mRNA and enzyme amounts in adult rat tissues. Biochim Biophys Acta. 1986 Jan 15;880(1):78–90. doi: 10.1016/0304-4165(86)90122-4. [DOI] [PubMed] [Google Scholar]
- DiMauro S., Arnold S., Miranda A., Rowland L. P. McArdle disease: the mystery of reappearing phosphorylase activity in muscle culture--a fetal isoenzyme. Ann Neurol. 1978 Jan;3(1):60–66. doi: 10.1002/ana.410030109. [DOI] [PubMed] [Google Scholar]
- DiMauro S., Hartwig G. B., Hays A., Eastwood A. B., Franco R., Olarte M., Chang M., Roses A. D., Fetell M., Schoenfeldt R. S. Debrancher deficiency: neuromuscular disorder in 5 adults. Ann Neurol. 1979 May;5(5):422–436. doi: 10.1002/ana.410050504. [DOI] [PubMed] [Google Scholar]
- Dreyfus J. C., Alexandre Y. Immunological studies on glycogen storage diseases type 3 and V. Demonstration of the presence of an immunoreactive protein in one case of muscle phosphorylase deficiency. Biochem Biophys Res Commun. 1971 Sep 17;44(6):1364–1370. doi: 10.1016/s0006-291x(71)80236-x. [DOI] [PubMed] [Google Scholar]
- Fanin M., Hoffman E. P., Saad F. A., Martinuzzi A., Danieli G. A., Angelini C. Dystrophin-positive myotubes in innervated muscle cultures from Duchenne and Becker muscular dystrophy patients. Neuromuscul Disord. 1993 Mar;3(2):119–127. doi: 10.1016/0960-8966(93)90003-3. [DOI] [PubMed] [Google Scholar]
- Feit H., Brooke M. H. Myophosphorylase deficiency: two different molecular etiologies. Neurology. 1976 Oct;26(10):963–967. doi: 10.1212/wnl.26.10.963. [DOI] [PubMed] [Google Scholar]
- Gautron S., Daegelen D., Mennecier F., Dubocq D., Kahn A., Dreyfus J. C. Molecular mechanisms of McArdle's disease (muscle glycogen phosphorylase deficiency). RNA and DNA analysis. J Clin Invest. 1987 Jan;79(1):275–281. doi: 10.1172/JCI112794. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gorin F. A., Mullinax R. L., Ignacio P. C., Neve R. L., Kurnit D. M. McArdle's & Hers' diseases: glycogen phosphorylase transcriptional expression in human tissues. J Neurogenet. 1987 Dec;4(6):293–308. [PubMed] [Google Scholar]
- Gorin F., Ignacio P., Gelinas R., Carlsen R. Abnormal expression of glycogen phosphorylase genes in regenerated muscle. Am J Physiol. 1989 Sep;257(3 Pt 1):C495–C503. doi: 10.1152/ajpcell.1989.257.3.C495. [DOI] [PubMed] [Google Scholar]
- Hughes R. J. A bioluminescent assay for glycogen phosphorylase in cultured cells. Anal Biochem. 1983 Jun;131(2):318–323. doi: 10.1016/0003-2697(83)90176-8. [DOI] [PubMed] [Google Scholar]
- Hwang P. K., See Y. P., Vincentini A. M., Powers M. A., Fletterick R. J., Crerar M. M. Comparative sequence analysis of rat, rabbit, and human muscle glycogen phosphorylase cDNAs. Eur J Biochem. 1985 Oct 15;152(2):267–274. doi: 10.1111/j.1432-1033.1985.tb09193.x. [DOI] [PubMed] [Google Scholar]
- LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
- Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
- Lebo R. V., Anderson L. A., DiMauro S., Lynch E., Hwang P., Fletterick R. Rare McArdle disease locus polymorphic site on 11q13 contains CpG sequence. Hum Genet. 1990 Nov;86(1):17–24. doi: 10.1007/BF00205166. [DOI] [PubMed] [Google Scholar]
- Lebo R. V., Gorin F., Fletterick R. J., Kao F. T., Cheung M. C., Bruce B. D., Kan Y. W. High-resolution chromosome sorting and DNA spot-blot analysis assign McArdle's syndrome to chromosome 11. Science. 1984 Jul 6;225(4657):57–59. doi: 10.1126/science.6587566. [DOI] [PubMed] [Google Scholar]
- Lockyer J. M., McCracken J. B., Jr Identification of a tissue-specific regulatory element within the human muscle glycogen phosphorylase gene. J Biol Chem. 1991 Oct 25;266(30):20262–20269. [PubMed] [Google Scholar]
- Martinuzzi A., Askanas V., Kobayashi T., Engel W. K. Asynchronous regulation of muscle specific isozymes of creatine kinase, glycogen phosphorylase, lactic dehydrogenase and phosphoglycerate mutase in innervated and non-innervated cultured human muscle. Neurosci Lett. 1988 Jun 29;89(2):216–222. doi: 10.1016/0304-3940(88)90384-9. [DOI] [PubMed] [Google Scholar]
- Martinuzzi A., Askanas V., Kobayashi T., Engel W. K., Di Mauro S. Expression of muscle-gene-specific isozymes of phosphorylase and creatine kinase in innervated cultured human muscle. J Cell Biol. 1986 Oct;103(4):1423–1429. doi: 10.1083/jcb.103.4.1423. [DOI] [PMC free article] [PubMed] [Google Scholar]
- McConchie S. M., Coakley J., Edwards R. H., Beynon R. J. Molecular heterogeneity in McArdle's disease. Biochim Biophys Acta. 1990 Nov 14;1096(1):26–32. doi: 10.1016/0925-4439(90)90008-d. [DOI] [PubMed] [Google Scholar]
- Meienhofer M. C., Askanas V., Proux-Daegelen D., Dreyfus J. C., Engel W. K. Muscle-type phosphorylase activity present in muscle cells cultured from three patients with myophosphorylase deficiency. Arch Neurol. 1977 Dec;34(12):779–781. doi: 10.1001/archneur.1977.00500240067013. [DOI] [PubMed] [Google Scholar]
- Mommaerts W. F., Illingworth B., Pearson C. M., Guillory R. J., Seraydarian K. A FUNCTIONAL DISORDER OF MUSCLE ASSOCIATED WITH THE ABSENCE OF PHOSPHORYLASE. Proc Natl Acad Sci U S A. 1959 Jun;45(6):791–797. doi: 10.1073/pnas.45.6.791. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Newgard C. B., Fletterick R. J., Anderson L. A., Lebo R. V. The polymorphic locus for glycogen storage disease VI (liver glycogen phosphorylase) maps to chromosome 14. Am J Hum Genet. 1987 Apr;40(4):351–364. [PMC free article] [PubMed] [Google Scholar]
- Newgard C. B., Littman D. R., van Genderen C., Smith M., Fletterick R. J. Human brain glycogen phosphorylase. Cloning, sequence analysis, chromosomal mapping, tissue expression, and comparison with the human liver and muscle isozymes. J Biol Chem. 1988 Mar 15;263(8):3850–3857. [PubMed] [Google Scholar]
- Pontecorvi A., Tata J. R., Phyillaier M., Robbins J. Selective degradation of mRNA: the role of short-lived proteins in differential destabilization of insulin-induced creatine phosphokinase and myosin heavy chain mRNAs during rat skeletal muscle L6 cell differentiation. EMBO J. 1988 May;7(5):1489–1495. doi: 10.1002/j.1460-2075.1988.tb02967.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Proux D., Dreyfus J. C. Phosphorylase isoenzymes in tissues: prevalence of the liver type in man. Clin Chim Acta. 1973 Oct 12;48(2):167–172. doi: 10.1016/0009-8981(73)90362-8. [DOI] [PubMed] [Google Scholar]
- Richter F., Böhme H. J., Hofmann E. Developmental changes of glycogen phosphorylase b isozymes in rat tissues. Biomed Biochim Acta. 1983;42(10):1229–1235. [PubMed] [Google Scholar]
- Roelofs R. I., Engel W. K., Chauvin P. B. Histochemical phosphorylase activity in regenerating muscle fibers from myophosphorylase-deficient patients. Science. 1972 Sep 1;177(4051):795–797. doi: 10.1126/science.177.4051.795. [DOI] [PubMed] [Google Scholar]
- Rutherford C. L., Peery R. B., Sucic J. F., Yin Y. Z., Rogers P. V., Luo S., Selmin O. Cloning, structural analysis, and expression of the glycogen phosphorylase-2 gene in Dictyostelium. J Biol Chem. 1992 Feb 5;267(4):2294–2302. [PubMed] [Google Scholar]
- SCHMID R., MAHLER R. Chronic progressive myopathy with myoglobinuria: demonstration of a glycogenolytic defect in the muscle. J Clin Invest. 1959 Nov;38:2044–2058. doi: 10.1172/JCI103983. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sato K., Imai F., Hatayama I., Roelofs R. I. Characterization of glycogen phosphorylase isoenzymes present in cultured skeletal muscle from patients with McArdle's disease. Biochem Biophys Res Commun. 1977 Sep 23;78(2):663–668. doi: 10.1016/0006-291x(77)90230-3. [DOI] [PubMed] [Google Scholar]
- Sato T., Sato K. Microheterogeneity of rat glycogen phosphorylase liver-type isozyme. Biochim Biophys Acta. 1980 Apr 11;612(2):344–351. doi: 10.1016/0005-2744(80)90117-5. [DOI] [PubMed] [Google Scholar]
- Servidei S., Shanske S., Zeviani M., Lebo R., Fletterick R., DiMauro S. McArdle's disease: biochemical and molecular genetic studies. Ann Neurol. 1988 Dec;24(6):774–781. doi: 10.1002/ana.410240612. [DOI] [PubMed] [Google Scholar]