Sensitive assay for mitochondrial DNA polymerase γ

被引:0
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作者
Naviaux, RK
Markusic, D
Barshop, BA
Nyhan, WL
Haas, RH
机构
[1] Univ Calif San Diego, Sch Med, Mitochondrial & Metab Dis Ctr, Dept Med, San Diego, CA 92103 USA
[2] Univ Calif San Diego, Sch Med, Mitochondrial & Metab Dis Ctr, Dept Neurosci, San Diego, CA 92103 USA
[3] Univ Calif San Diego, Sch Med, Mitochondrial & Metab Dis Ctr, Dept Pediat, San Diego, CA 92103 USA
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中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: The mitochondrial DNA polymerase gamma is the principal polymerase required for mitochondrial DNA replication. Primary or secondary deficiencies in the activity of DNA polymerase gamma may lead to mitochondrial DNA depletion. We describe a sensitive and robust clinical assay for this enzyme. Methods: The assay was performed on mitochondria isolated from skeletal muscle biopsies. High-molecular weight polynucleotide reaction products were captured on ion-exchange paper, examined qualitatively by autoradiography, and quantified by scintillation counting. Results: Kinetic analysis of DNA polymerase gamma by this method showed a K-m for dTTP of 1.43 mu mol/L, and a K-i for azidothymidine triphosphate of 0.861 mu mol/L. The assay was linear from 0.1 to 2 mu g of mitochondrial protein. The detection limit was 30 units (30 fmol dTMP incorporated in 30 min). The linear dynamic range was three orders of magnitude; 30-30 000 units. Imprecision (CV) was 6.4% within day and 12% between days. Application of this assay to a mixed population of 38 patients referred for evaluation of mitochondrial disease revealed a distribution with a range of 0-2506 U/mu g, reflecting extensive biologic variation among patients with neuromuscular disease. Conclusion: This assay provides a useful adjunct to current laboratory methods for the evaluation of patients with suspected mitochondrial DNA depletion syndromes. (C) 1999 American Association for Clinical Chemistry.
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页码:1725 / 1733
页数:9
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