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. 1983 Nov;72(5):1543–1552. doi: 10.1172/JCI111113

Complementation studies of isovaleric acidemia and glutaric aciduria type II using cultured skin fibroblasts.

B Dubiel, C Dabrowski, R Wetts, K Tanaka
PMCID: PMC370442  PMID: 6630517

Abstract

Using cultured skin fibroblasts, we studied the heterogeneity of inborn errors of leucine metabolism such as isovaleric acidemia (IVA), glutaric aciduria type II (GA II), and multiple carboxylase deficiency (MC). We first developed a simple macromolecular-labeling test to measure the ability of cells to oxidize [1-14C]isovaleric acid in situ in culture. Cells from two different lines were fused using polyethylene glycol, and the ability of the heterokaryons to oxidize [1-14C]isovaleric acid was tested by the macromolecular-labeling test. The MC line complemented with all 10 IVA lines tested; heterokaryons showed 99 +/- 68% more activity than the unfused mixture of component cells. GA II/IVA heterokaryons exhibited poor growth, but when the culture remained confluent, the GA II cells complemented with all six IVA lines tested, showing a 71 +/- 41% increase in activity. The relatively large standard deviations are due to a few experiments in which significant enhancement of macromolecular-labeling test activity was not observed upon fusion, but significant complementation was clearly observed in repeats of the same combinations. These results are consistent with our previous findings, which indicated that the decreased ability of GA II cells to oxidize isovaleryl-CoA involves a defective electron-transporting system rather than a defective isovaleryl-CoA dehydrogenase. IVA/IVA heterokaryons showed no complementation in any combination tested, indicating no detectable heterogeneity in isovaleric acidemia. This finding indicates that the same gene is mutated in all IVA lines. Previous results indicated that this gene codes for isovaleryl-CoA dehydrogenase.

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Selected References

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  1. Blaskovics M. E., Ng W. G., Donnell G. N. Prenatal diagnosis and a case report of isovaleric acidaemia. J Inherit Metab Dis. 1978;1(1):9–11. doi: 10.1007/BF01805706. [DOI] [PubMed] [Google Scholar]
  2. Budd M. A., Tanaka K., Holmes L. B., Efron M. L., Crawford J. D., Isselbacher K. J. Isovaleric acidemia. Clinical features of a new genetic defect of leucine metabolism. N Engl J Med. 1967 Aug 17;277(7):321–327. doi: 10.1056/NEJM196708172770701. [DOI] [PubMed] [Google Scholar]
  3. Dusheiko G., Kew M. C., Joffe B. I., Lewin J. R., Mantagos S., Tanaka K. Recurrent hypoglycemia associated with glutaric aciduria type II in an adult. N Engl J Med. 1979 Dec 27;301(26):1405–1409. doi: 10.1056/NEJM197912273012601. [DOI] [PubMed] [Google Scholar]
  4. Goodman S. I., McCabe E. R., Fennessey P. V., Mace J. W. Multiple acyl-CoA dehydrogenase deficiency (glutaric aciduria type II) with transient hypersarcosinemia and sarcosinuria; possible inherited deficiency of an electron transfer flavoprotein. Pediatr Res. 1980 Jan;14(1):12–17. doi: 10.1203/00006450-198001000-00004. [DOI] [PubMed] [Google Scholar]
  5. Gravel R. A., Lam K. F., Scully K. J., Hsia Y. Genetic complementation of propionyl-CoA carboxylase deficiency in cultured human fibroblasts. Am J Hum Genet. 1977 Jul;29(4):378–388. [PMC free article] [PubMed] [Google Scholar]
  6. Gravel R. A., Mahoney M. J., Ruddle F. H., Rosenberg L. E. Genetic complementation in heterokaryons of human fibroblasts defective in cobalamin metabolism. Proc Natl Acad Sci U S A. 1975 Aug;72(8):3181–3185. doi: 10.1073/pnas.72.8.3181. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Hill H. Z., Puck T. T. Detection of inborn errors of metabolism: galactosemia. Science. 1973 Mar 16;179(4078):1136–1139. doi: 10.1126/science.179.4078.1136. [DOI] [PubMed] [Google Scholar]
  8. Ikeda Y., Dabrowski C., Tanaka K. Separation and properties of five distinct acyl-CoA dehydrogenases from rat liver mitochondria. Identification of a new 2-methyl branched chain acyl-CoA dehydrogenase. J Biol Chem. 1983 Jan 25;258(2):1066–1076. [PubMed] [Google Scholar]
  9. Ikeda Y., Tanaka K. Purification and characterization of isovaleryl coenzyme A dehydrogenase from rat liver mitochondria. J Biol Chem. 1983 Jan 25;258(2):1077–1085. [PubMed] [Google Scholar]
  10. Kalousek F., Darigo M. D., Rosenberg L. E. Isolation and characterization of propionyl-CoA carboxylase from normal human liver. Evidence for a protomeric tetramer of nonidentical subunits. J Biol Chem. 1980 Jan 10;255(1):60–65. [PubMed] [Google Scholar]
  11. Kelleher J. F., Jr, Yudkoff M., Hutchinson R., August C. S., Cohn R. M. The pancytopenia of isovaleric acidemia. Pediatrics. 1980 May;65(5):1023–1027. [PubMed] [Google Scholar]
  12. Krieger I., Tanaka K. Therapeutic effects of glycine in isovaleric acidemia. Pediatr Res. 1976 Jan;10(1):25–29. doi: 10.1203/00006450-197601000-00005. [DOI] [PubMed] [Google Scholar]
  13. 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]
  14. Lyons L. B., Cox R. P., Dancis J. Complementation analysis of maple syrup urine disease in heterokaryons derived from cultured human fibroblasts. Nature. 1973 Jun 29;243(5409):533–535. doi: 10.1038/243533a0. [DOI] [PubMed] [Google Scholar]
  15. Mantagos S., Genel M., Tanaka K. Ethylmalonic-adipic aciduria. In vivo and in vitro studies indicating deficiency of activities of multiple acyl-CoA dehydrogenases. J Clin Invest. 1979 Dec;64(6):1580–1589. doi: 10.1172/JCI109619. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Newman C. G., Wilson B. D., Callaghan P., Young L. Neonatal death associated with isovalericacidaemia. Lancet. 1967 Aug 26;2(7513):439–442. doi: 10.1016/s0140-6736(67)90854-9. [DOI] [PubMed] [Google Scholar]
  17. Przyrembel H., Wendel U., Becker K., Bremer H. J., Bruinvis L., Ketting D., Wadman S. K. Glutaric aciduria type II: report on a previously undescribed metabolic disorder. Clin Chim Acta. 1976 Jan 16;66(2):227–239. doi: 10.1016/0009-8981(76)90060-7. [DOI] [PubMed] [Google Scholar]
  18. Rhead W. J., Tanaka K. Demonstration of a specific mitochondrial isovaleryl-CoA dehydrogenase deficiency in fibroblasts from patients with isovaleric acidemia. Proc Natl Acad Sci U S A. 1980 Jan;77(1):580–583. doi: 10.1073/pnas.77.1.580. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Rhead W., Mantagos S., Tanaka K. Glutaric aciduria type II: in vitro studies on substrate oxidation, acyl-CoA dehydrogenases, and electron-transferring flavoprotein in cultured skin fibroblasts. Pediatr Res. 1980 Dec;14(12):1339–1342. doi: 10.1203/00006450-198012000-00013. [DOI] [PubMed] [Google Scholar]
  20. Roth K., Cohn R., Yandrasitz J., Preti G., Dodd P., Segal S. Beta-methylcrotonic aciduria associated with lactic acidosis. J Pediatr. 1976 Feb;88(2):229–235. doi: 10.1016/s0022-3476(76)80987-0. [DOI] [PubMed] [Google Scholar]
  21. Saudubray J. M., Sorin M., Depondt E., Herouin C., Charpentier C., Pousset J. L. Acidémie isovalérique. Etude et traitement chez trois freres. Arch Fr Pediatr. 1976 Oct;33(8):795–808. [PubMed] [Google Scholar]
  22. Saunders M., Sweetman L., Robinson B., Roth K., Cohn R., Gravel R. A. Biotin-response organicaciduria. Multiple carboxylase defects and complementation studies with propionicacidemia in cultured fibroblasts. J Clin Invest. 1979 Dec;64(6):1695–1702. doi: 10.1172/JCI109632. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Schneiderman S., Farber J. L., Baserga R. A simple method for decreasing the toxicity of polyethylene glycol in mammalian cell hybridization. Somatic Cell Genet. 1979 Mar;5(2):263–269. doi: 10.1007/BF01539165. [DOI] [PubMed] [Google Scholar]
  24. Spirer Z., Swirsky-Fein S., Zakut V., Legum C., Bogair N., Charles R., Gil-Av E. Acute neonatal isovaleric acidemia. A report of two cases. Isr J Med Sci. 1975 Oct;11(10):1005–1010. [PubMed] [Google Scholar]
  25. Tanaka K., Budd M. A., Efron M. L., Isselbacher K. J. Isovaleric acidemia: a new genetic defect of leucine metabolism. Proc Natl Acad Sci U S A. 1966 Jul;56(1):236–242. doi: 10.1073/pnas.56.1.236. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Tanaka K., Isselbacher K. J. The isolation and identification of N-isovalerylglycine from urine of patients with isovaleric acidemia. J Biol Chem. 1967 Jun 25;242(12):2966–2972. [PubMed] [Google Scholar]
  27. Tanaka K., Mandell R., Shih V. E. Metabolism of [1-(14)C] and [2-(14)C] leucine in cultured skin fibroblasts from patients with isovaleric acidemia. Characterization of metabolic defects. J Clin Invest. 1976 Jul;58(1):164–172. doi: 10.1172/JCI108446. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Truscott R. J., Malegan D., McCairns E., Burke D., Hick L., Sims P., Halpern B., Tanaka K., Sweetman L., Nyhan W. L. New metabolites in isovaleric acidemia. Clin Chim Acta. 1981 Mar 5;110(2-3):187–203. doi: 10.1016/0009-8981(81)90348-x. [DOI] [PubMed] [Google Scholar]
  29. Van Leeuwen G. H., De Vrieze G., Gimpel J. A., Huisjes H. J., Hommes F. A. Cell genetic studies on propionyl-CoA carboxylase deficient cell lines. J Inherit Metab Dis. 1982;5(2):115–120. doi: 10.1007/BF01800004. [DOI] [PubMed] [Google Scholar]
  30. Willard H. F., Ambani L. M., Hart A. C., Mahoney M. J., Rosenberg L. E. Rapid prenatal and postnatal detection of inborn errors of propionate, methylmalonate, and cobalamin metabolism: a sensitive assay using cultured cells. Hum Genet. 1976 Dec 15;34(3):277–283. doi: 10.1007/BF00295291. [DOI] [PubMed] [Google Scholar]
  31. Willard H. F., Mellman I. S., Rosenberg L. E. Genetic complementation among inherited deficiencies of methylmalonyl-CoA mutase activity: evidence for a new class of human cobalamin mutant. Am J Hum Genet. 1978 Jan;30(1):1–13. [PMC free article] [PubMed] [Google Scholar]

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