A pathogenic 15-base pair deletion in mitochondrial DNA-encoded cytochrome c oxidase subunit III results in the absence of functional cytochrome c oxidase
| Autor: | Nancy G. Kennaway, Edgar Davidson, Kristen C. Hoffbuhr, Michael P. King, Mercy M. Davidson, Beth A. Filiano |
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| Rok vydání: | 2000 |
| Předmět: |
Oxidase test
Mitochondrial DNA Mutation Cytochrome c oxidase subunit III Protein subunit Respiratory chain Cell Biology Gene mutation Biology medicine.disease_cause Biochemistry Molecular biology DNA Mitochondrial Electron Transport Complex IV medicine biology.protein Tumor Cells Cultured Cytochrome c oxidase Humans Molecular Biology Sequence Deletion |
| Zdroj: | The Journal of biological chemistry. 275(18) |
| ISSN: | 0021-9258 |
| Popis: | A 15-base pair, in-frame, deletion (9480del15) in the mitochondrial DNA (mtDNA)-encoded cytochrome c oxidase subunit III (COX III) gene was identified previously in a patient with recurrent episodes of myoglobinuria and an isolated COX deficiency. Transmitochondrial cell lines harboring 0, 97, and 100% of the 9480del15 deletion were created by fusing human cells lacking mtDNA (rho(0) cells) with platelet and lymphocyte fractions isolated from the patient. The COX III gene mutation resulted in a severe respiratory chain defect in all mutant cell lines. Cells homoplasmic for the mutation had no detectable COX activity or respiratory ATP synthesis, and required uridine and pyruvate supplementation for growth, a phenotype similar to rho(0) cells. The cells with 97% mutated mtDNA exhibited severe reductions in both COX activity (6% of wild-type levels) and rates of ATP synthesis (9% of wild-type). The COX III polypeptide in the mutant cells, although translated at rates similar to wild-type, had reduced stability. There was no evidence for assembly of COX I, COX II, or COX III subunits in a multisubunit complex in cells homoplasmic for the mutation, thus indicating that there was no stable assembly of COX I with COX II in the absence of wild-type COX III. In contrast, the COX I and COX II subunits were assembled in cells with 97% mutated mtDNA. |
| Databáze: | OpenAIRE |
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