Genetic test for myophosphorylase deficiency in Charolais cattle

American Journal of Veterinary Research

Volumn 59, Issue 3, 1998, Pages 267-270

  Bilstrom, Jessica A ^a   Valberg, Stephanie J ^a   Bernoco, Domenico ^b   Mickelson, James R ^a  

^a UNIVERSITY OF MINNESOTA   (United States)

^b Stormont Laboratories   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; PHOSPHORYLASE;

ANIMAL; ARTICLE; BLOOD; CATTLE; CODON; EXON; FEMALE; GENETICS; GENOTYPE; INTRON; MALE; METHODOLOGY; MOLECULAR GENETICS; NUCLEOTIDE SEQUENCE; PEDIGREE; POINT MUTATION; POLYMERASE CHAIN REACTION; SPECIES DIFFERENCE;

ANIMALS; BASE SEQUENCE; CATTLE; CODON; DNA; EXONS; FEMALE; GENOTYPE; INTRONS; MALE; MOLECULAR SEQUENCE DATA; PEDIGREE; PHOSPHORYLASES; POINT MUTATION; POLYMERASE CHAIN REACTION; SPECIES SPECIFICITY;

EID: 0032014732     PISSN: 00029645     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (12)

1. Osawa S, Chiu RH, McDonough A, et al. Isolation of partial cDNAs for rat liver and muscle glycogen phosphorylase isozymes. FEBS Lett 1986;702:282-288.
2. DiMauro S, Tsujino S. Glycogenoses. In: Engel AG, Franzini-Armstrong C, eds. Myology. 2nd ed. New York: McGraw-Hill, 1994;1554-1576.
3. McArdle B. Myopathy due to a defect in muscle glycogen breakdown. Clin Sci 1951;10:13-33.
4. Angelos S, Valberg SJ, Smith BP, et al. Myophosphorylase deficiency associated with rhabdomyolysis and exercise intolerance in 6 related Charolais cattle. Muscle Nerve 1995;18:736-740.
5. Tsujino S, Shanske S, Valberg SJ, et al. Cloning of bovine muscle glycogen phosphorylase cDNA and identification of a mutation in cattle with myophosphorylase deficiency, an animal model for McArdle's disease. Neuromuscul Disord 1995;6:19-26.
6. Stormont C. Contribution of blood typing to dairy science progress. J Dairy Sci 1967;50:253-260.
7. Burke J, Hwang P, Anderson L, et al. Intron/exon structure of the human gene for the muscle isoenzyme of glycogen phosphorylase. Proteins 1987;2:177-187.
8. Hwang PK, See YP, Vincentini AM, et al. Compared sequence analysis of rat, rabbit, and human muscle glycogen phosphorylase cDNA. Eur J Biochem 1985;152:267-274.
9. Tsujino S, Shanske S, DiMauro S. Molecular genetic heterogeneity of myophosphorylase deficiency (McArdle's Disease). N Engl J Med 1993;329:241-245.
10. Hodgon DH, Parish S. Diseases of muscle. In: Smith BP, ed. Large animal internal medicine. St Louis, MO: CV Mosby Co, 1990;1335-1360.
11. Smith BF, Stedman H, Rajpurohit Y, et al. Molecular basis of canine muscle type phosphofructokinase deficiency. J Biol Chem 1996;271:20070-20074.
12. Fyfe JC, Giger U, Van Winkle TJ, et al. Glycogen storage disease type IV: inherited deficiency of branching enzyme activity in cats. Pediatr Res 1992;32:719-725.