Literature DB >> 20149659

A novel mutation in the tRNAIle gene (MTTI) affecting the variable loop in a patient with chronic progressive external ophthalmoplegia (CPEO).

Andres Berardo1, Jorida Coku, Bulent Kurt, Salvatore DiMauro, Michio Hirano.   

Abstract

We describe a 62-year-old woman with chronic progressive external ophthalmoplegia (CPEO), multiple lipomas, diabetes mellitus, and a novel mitochondrial DNA (mtDNA) mutation at nucleotide 4302 (4302A>G) of the tRNA(Ile) gene (MTTI). This is the first mutation at position 44 in the variable loop (V loop) of any mitochondrial tRNA. The muscle biopsy revealed 10% ragged-red/ragged-blue fibers and 25% cytochrome c oxidase (COX)-deficient fibers. No deletions or duplications were detected by Southern blot analysis. The 4302A>G transition was present only in the patient's muscle and single-fiber analysis revealed significantly higher levels of the mutation in COX-deficient than in normal fibers. Like tRNA(Leu(UUR)), tRNA(Ile) appears to be a "hot spot" for mtDNA mutations causing CPEO. Copyright 2010 Elsevier B.V. All rights reserved.

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Year:  2010        PMID: 20149659      PMCID: PMC2841220          DOI: 10.1016/j.nmd.2010.01.006

Source DB:  PubMed          Journal:  Neuromuscul Disord        ISSN: 0960-8966            Impact factor:   4.296


  20 in total

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4.  A novel mutation in the mitochondrial tRNA for tryptophan causing a late-onset mitochondrial encephalomyopathy.

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5.  Mitochondrial myopathies: clinical and biochemical features of 30 patients with major deletions of muscle mitochondrial DNA.

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9.  A novel mitochondrial DNA point mutation in the tRNA(Ile) gene is associated with progressive external ophtalmoplegia.

Authors:  G Silvestri; S Servidei; M Rana; E Ricci; A Spinazzola; E Paris; P Tonali
Journal:  Biochem Biophys Res Commun       Date:  1996-03-27       Impact factor: 3.575

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  6 in total

1.  Impairment of mitochondrial tRNAIle processing by a novel mutation associated with chronic progressive external ophthalmoplegia.

Authors:  A Schaller; R Desetty; D Hahn; C B Jackson; J-M Nuoffer; S Gallati; L Levinger
Journal:  Mitochondrion       Date:  2011-02-01       Impact factor: 4.160

2.  Mitochondrial DNA abnormalities in ophthalmological disease.

Authors:  Grainne S Gorman; Robert W Taylor
Journal:  Saudi J Ophthalmol       Date:  2011-02-18

3.  Atheromatosis of the Scalp: A Novel Feature of Chronic Progressive External Ophthalmoplegia Plus Due to a Single Mitochondrial DNA Deletion.

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Journal:  Cureus       Date:  2021-12-23

Review 4.  Cardiological manifestations of mitochondrial respiratory chain disorders.

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Review 5.  Transfer RNA and human disease.

Authors:  Jamie A Abbott; Christopher S Francklyn; Susan M Robey-Bond
Journal:  Front Genet       Date:  2014-06-03       Impact factor: 4.599

6.  Disclosing the functional changes of two genetic alterations in a patient with Chronic Progressive External Ophthalmoplegia: Report of the novel mtDNA m.7486G>A variant.

Authors:  Mafalda Bacalhau; Marta Simões; Mariana C Rocha; Steven A Hardy; Amy E Vincent; João Durães; Maria C Macário; Maria João Santos; Olinda Rebelo; Carla Lopes; João Pratas; Cândida Mendes; Mónica Zuzarte; A Cristina Rego; Henrique Girão; Lee-Jun C Wong; Robert W Taylor; Manuela Grazina
Journal:  Neuromuscul Disord       Date:  2017-11-23       Impact factor: 4.296

  6 in total

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