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A mutant mitochondrial respiratory chain assembly protein causes complex III deficiency in patients with tubulopathy, encephalopathy and liver failure.
de Lonlay, P; Valnot, I; Barrientos, A; Gorbatyuk, M; Tzagoloff, A; Taanman, J W; Benayoun, E; Chrétien, D; Kadhom, N; Lombès, A; de Baulny, H O; Niaudet, P; Munnich, A; Rustin, P; Rötig, A.
Affiliation
  • de Lonlay P; INSERM U393, Hôpital Necker-Enfants Malades, 149 rue de Sèvres, 75015 Paris.
Nat Genet ; 29(1): 57-60, 2001 Sep.
Article in En | MEDLINE | ID: mdl-11528392
ABSTRACT
Complex III (CIII; ubiquinol cytochrome c reductase of the mitochondrial respiratory chain) catalyzes electron transfer from succinate and nicotinamide adenine dinucleotide-linked dehydrogenases to cytochrome c. CIII is made up of 11 subunits, of which all but one (cytochrome b) are encoded by nuclear DNA. CIII deficiencies are rare and manifest heterogeneous clinical presentations. Although pathogenic mutations in the gene encoding mitochondrial cytochrome b have been described, mutations in the nuclear-DNA-encoded subunits have not been reported. Involvement of various genes has been indicated in assembly of yeast CIII (refs. 8-11). So far only one such gene, BCS1L, has been identified in human. BCS1L represents, therefore, an obvious candidate gene in CIII deficiency. Here, we report BCS1L mutations in six patients, from four unrelated families and presenting neonatal proximal tubulopathy, hepatic involvement and encephalopathy. Complementation study in yeast confirmed the deleterious effect of these mutations. Mutation of BCS1L would seem to be a frequent cause of CIII deficiency, as one-third of our patients have BCS1L mutations.
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Collection: 01-internacional Database: MEDLINE Main subject: Brain Diseases / Proteins / Liver Failure / Electron Transport Complex III / Electron Transport / Kidney Tubules, Proximal / Mitochondria / Mutation Type of study: Etiology_studies Limits: Animals / Female / Humans / Male / Newborn Language: En Journal: Nat Genet Journal subject: GENETICA MEDICA Year: 2001 Document type: Article
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Collection: 01-internacional Database: MEDLINE Main subject: Brain Diseases / Proteins / Liver Failure / Electron Transport Complex III / Electron Transport / Kidney Tubules, Proximal / Mitochondria / Mutation Type of study: Etiology_studies Limits: Animals / Female / Humans / Male / Newborn Language: En Journal: Nat Genet Journal subject: GENETICA MEDICA Year: 2001 Document type: Article