Literature DB >> 1656694

Chronic progressive external ophthalmoplegia in patients with large heteroplasmic mitochondrial DNA deletions: an immunocytochemical study.

S Collins1, X Dennett, E Byrne, S Marzuki.   

Abstract

Immunocytochemical studies with a holocomplex antibody battery in patients with chronic progressive external ophthalmoplegia, with and without large mitochondrial DNA deletions, revealed positive (and often increased) immunoreactivity for all complexes studied in histochemically cytochrome oxidase (COX)-negative areas, suggesting a compensatory up-regulation of these components. Similar findings were observed with subunit-specific probes directed against both nuclear- and mitochondrially encoded gene products. Comparison of staining intensities between the different complexes revealed significantly more variability in COX-negative than COX-positive fibres, suggesting disordered stoichiometric control during up-regulation. These differences were confirmed using statistical models. This data challenges the view that COX-negative fibre segments have little or no mitochondrially coded protein translation.

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Year:  1991        PMID: 1656694     DOI: 10.1007/bf00294444

Source DB:  PubMed          Journal:  Acta Neuropathol        ISSN: 0001-6322            Impact factor:   17.088


  36 in total

1.  Partial cytochrome oxidase (aa3) deficiency in chronic progressive external ophthalmoplegia. Histochemical and biochemical studies.

Authors:  E Byrne; X Dennett; I Trounce; R Henderson
Journal:  J Neurol Sci       Date:  1985-12       Impact factor: 3.181

2.  Immunocytochemical studies of cytochrome oxidase subunits in skeletal muscle of patients with partial cytochrome oxidase deficiencies.

Authors:  M A Johnson; B Kadenbach; M Droste; S L Old; D M Turnbull
Journal:  J Neurol Sci       Date:  1988-10       Impact factor: 3.181

3.  Partial cytochrome oxidase deficiency without subsarcolemmal accumulation of mitochondria in chronic progressive external ophthalmoplegia.

Authors:  D M Turnbull; M A Johnson; D J Dick; N E Cartlidge; H S Sherratt
Journal:  J Neurol Sci       Date:  1985-08       Impact factor: 3.181

4.  Atypical muscle mitochondria in oculoskeletal myopathy.

Authors:  J A Morgan-Hughes; W G Mair
Journal:  Brain       Date:  1973-06       Impact factor: 13.501

5.  Ophthalmoplegia plus. The neurodegenerative disorders associated with progressive external ophthalmoplegia.

Authors:  D A Drachman
Journal:  Arch Neurol       Date:  1968-06

6.  Partial deficiency of subunits in complex I or IV of patients with mitochondrial myopathies.

Authors:  M Tanaka; M Nishikimi; H Suzuki; T Ozawa; Y Koga; I Nonaka
Journal:  Biochem Int       Date:  1987-03

7.  Fatal mitochondrial cardiomyopathy in Kearns-Sayre syndrome with deficiency of cytochrome-c-oxidase in cardiac and skeletal muscle. An enzymehistochemical--ultra-immunocytochemical--fine structural study in longterm frozen autopsy tissue.

Authors:  J Müller-Höcker; A Johannes; M Droste; B Kadenbach; D Pongratz; G Hübner
Journal:  Virchows Arch B Cell Pathol Incl Mol Pathol       Date:  1986

8.  Assignment of two mitochondrially synthesized polypeptides to human mitochondrial DNA and their use in the study of intracellular mitochondrial interaction.

Authors:  N A Oliver; D C Wallace
Journal:  Mol Cell Biol       Date:  1982-01       Impact factor: 4.272

9.  Sequence and organization of the human mitochondrial genome.

Authors:  S Anderson; A T Bankier; B G Barrell; M H de Bruijn; A R Coulson; J Drouin; I C Eperon; D P Nierlich; B A Roe; F Sanger; P H Schreier; A J Smith; R Staden; I G Young
Journal:  Nature       Date:  1981-04-09       Impact factor: 49.962

10.  Detection of "deleted" mitochondrial genomes in cytochrome-c oxidase-deficient muscle fibers of a patient with Kearns-Sayre syndrome.

Authors:  S Mita; B Schmidt; E A Schon; S DiMauro; E Bonilla
Journal:  Proc Natl Acad Sci U S A       Date:  1989-12       Impact factor: 11.205

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  2 in total

1.  Microphotometric analysis of NADH-tetrazolium reductase deficiency in fibroblasts of patients with Leber hereditary optic neuropathy.

Authors:  S Malik; H Sudoyo; S Marzuki
Journal:  J Inherit Metab Dis       Date:  2000-11       Impact factor: 4.982

Review 2.  Molecular biology of neurological diseases.

Authors:  W J Cumming
Journal:  Postgrad Med J       Date:  1992-04       Impact factor: 2.401

  2 in total

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