Literature DB >> 2559245

Cytochrome c oxidase deficiency in subacute necrotizing encephalopathy (Leigh syndrome).

K Hayasaka1, G K Brown, D M Danks, M Droste, B Kadenbach.   

Abstract

Tissues and cultured fibroblasts from two patients with Leigh syndrome (subacute necrotizing encephalopathy) were examined. A systemic defect in cytochrome oxidase was identified by enzyme assay and estimation of cytochrome concentrations. Immunochemical analysis showed a reduction of most subunits of the cytochrome oxidase complex. The rate of synthesis of cytochrome oxidase subunits, determined by labelling experiments in cultured fibroblasts, was the same in the patients and normal controls. The reduced cytochrome oxidase content of the patients' tissues must therefore result from abnormal turnover of the protein subunits.

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Year:  1989        PMID: 2559245     DOI: 10.1007/BF01799214

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  21 in total

1.  Preparation and properties of complex V.

Authors:  D L Stiggall; Y M Galante; Y Hatefi
Journal:  Methods Enzymol       Date:  1979       Impact factor: 1.600

2.  Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications.

Authors:  H Towbin; T Staehelin; J Gordon
Journal:  Proc Natl Acad Sci U S A       Date:  1979-09       Impact factor: 11.205

3.  Subacute necrotizing encephalomyelopathy (Leigh's disease): a consideration of clinical features and etiology.

Authors:  J H Pincus
Journal:  Dev Med Child Neurol       Date:  1972-02       Impact factor: 5.449

4.  Six unidentified reading frames of human mitochondrial DNA encode components of the respiratory-chain NADH dehydrogenase.

Authors:  A Chomyn; P Mariottini; M W Cleeter; C I Ragan; A Matsuno-Yagi; Y Hatefi; R F Doolittle; G Attardi
Journal:  Nature       Date:  1985 Apr 18-24       Impact factor: 49.962

Review 5.  On the function of multiple subunits of cytochrome c oxidase from higher eukaryotes.

Authors:  B Kadenbach; P Merle
Journal:  FEBS Lett       Date:  1981-11-30       Impact factor: 4.124

6.  The subunit composition of mammalian cytochrome c oxidase.

Authors:  P Merle; B Kadenbach
Journal:  Eur J Biochem       Date:  1980-04

7.  Pyruvate dehydrogenase complex deficiency as a cause of subacute necrotizing encephalopathy (Leigh disease).

Authors:  H A Kretzschmar; S J DeArmond; T K Koch; M S Patel; C J Newth; K A Schmidt; S Packman
Journal:  Pediatrics       Date:  1987-03       Impact factor: 7.124

8.  Assembly of the mitochondrial membrane system. CBP1, a yeast nuclear gene involved in 5' end processing of cytochrome b pre-mRNA.

Authors:  C L Dieckmann; T J Koerner; A Tzagoloff
Journal:  J Biol Chem       Date:  1984-04-25       Impact factor: 5.157

9.  Malonyl coenzyme A decarboxylase deficiency.

Authors:  G K Brown; R D Scholem; A Bankier; D M Danks
Journal:  J Inherit Metab Dis       Date:  1984       Impact factor: 4.982

10.  Molecular heterogeneity of variant isovaleryl-CoA dehydrogenase from cultured isovaleric acidemia fibroblasts.

Authors:  Y Ikeda; S M Keese; K Tanaka
Journal:  Proc Natl Acad Sci U S A       Date:  1985-10       Impact factor: 11.205

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  4 in total

1.  Complementation analysis of systemic cytochrome oxidase deficiency presenting as Leigh syndrome.

Authors:  R M Brown; G K Brown
Journal:  J Inherit Metab Dis       Date:  1996       Impact factor: 4.982

2.  Diagnostic difficulties with common SURF1 mutations in patients with cytochrome oxidase-deficient Leigh syndrome.

Authors:  R A Head; R M Brown; G K Brown
Journal:  J Inherit Metab Dis       Date:  2004       Impact factor: 4.982

3.  Clinical, metabolic, and genetic aspects of cytochrome C oxidase deficiency in Saguenay-Lac-Saint-Jean.

Authors:  C Morin; G Mitchell; J Larochelle; M Lambert; H Ogier; B H Robinson; M De Braekeleer
Journal:  Am J Hum Genet       Date:  1993-08       Impact factor: 11.025

4.  HIBCH mutations can cause Leigh-like disease with combined deficiency of multiple mitochondrial respiratory chain enzymes and pyruvate dehydrogenase.

Authors:  Sacha Ferdinandusse; Hans R Waterham; Simon J R Heales; Garry K Brown; Iain P Hargreaves; Jan-Willem Taanman; Roxana Gunny; Lara Abulhoul; Ronald J A Wanders; Peter T Clayton; James V Leonard; Shamima Rahman
Journal:  Orphanet J Rare Dis       Date:  2013-12-04       Impact factor: 4.123

  4 in total

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