Literature DB >> 2590206

Multiple deletions in mitochondrial DNA at direct repeats of non-D-loop regions in cases of familial mitochondrial myopathy.

M Yuzaki1, N Ohkoshi, I Kanazawa, Y Kagawa, S Ohta.   

Abstract

Muscle mitochondrial DNAs from two brothers with mitochondrial myopathy associated with peripheral neuropathy had multiple deletions, most of which started in non-D-loop regions, unlike in an autosomal dominant mitochondrial myopathy (Zeviani, M. et al., Nature 339, 309 (1989)). The non-D-loop regions with deletions were amplified by the polymerase chain reaction and the resulting fragments were subcloned and then sequenced. At least 12 deletions of different lengths in different sites were found. However, all the deletions were flanked by short direct repeats (4-12 base pairs).

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Year:  1989        PMID: 2590206     DOI: 10.1016/0006-291x(89)91818-4

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  17 in total

1.  Gene deletions causing human genetic disease: mechanisms of mutagenesis and the role of the local DNA sequence environment.

Authors:  M Krawczak; D N Cooper
Journal:  Hum Genet       Date:  1991-03       Impact factor: 4.132

2.  No mitochondrial DNA deletions but more D-loop point mutations in repeated pregnancy loss.

Authors:  Seyed Mohammad Seyedhassani; Massoud Houshmand; Seyed Mehdi Kalantar; Glayol Modabber; Abbas Aflatoonian
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3.  Autosomal recessive Wolfram syndrome associated with an 8.5-kb mtDNA single deletion.

Authors:  A Barrientos; J Casademont; A Saiz; F Cardellach; V Volpini; A Solans; E Tolosa; A Urbano-Marquez; X Estivill; V Nunes
Journal:  Am J Hum Genet       Date:  1996-05       Impact factor: 11.025

4.  Different in situ hybridization patterns of mitochondrial DNA in cytochrome c oxidase-deficient extraocular muscle fibres in the elderly.

Authors:  J Müller-Höcker; P Seibel; K Schneiderbanger; B Kadenbach
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1993

5.  The 9-bp deletion in region V of mitochondrial DNA: evidence of mutation recurrence.

Authors:  A Barrientos; J Casademont; A Solans; P Moral; F Cardellach; A Urbano-Márquez; X Estivill; V Nunes
Journal:  Hum Genet       Date:  1995-08       Impact factor: 4.132

6.  A nuclear defect in the 4p16 region predisposes to multiple mitochondrial DNA deletions in families with Wolfram syndrome.

Authors:  A Barrientos; V Volpini; J Casademont; D Genís; J M Manzanares; I Ferrer; J Corral; F Cardellach; A Urbano-Márquez; X Estivill; V Nunes
Journal:  J Clin Invest       Date:  1996-04-01       Impact factor: 14.808

Review 7.  Prospects for the genetics of human longevity.

Authors:  F Schächter; D Cohen; T Kirkwood
Journal:  Hum Genet       Date:  1993-07       Impact factor: 4.132

8.  Multiple sclerosis and mitochondrial myopathy: an unusual combination of diseases.

Authors:  L Bet; M Moggio; G P Comi; C Mariani; A Prelle; N Checcarelli; A Bordoni; N Bresolin; E Scarpini; G Scarlato
Journal:  J Neurol       Date:  1994-07       Impact factor: 4.849

9.  Encephalomyopathies caused by abnormal nuclear-mitochondrial intergenomic cross-talk.

Authors:  C Lamperti; M Zeviani
Journal:  Acta Myol       Date:  2009-07

Review 10.  Nucleus-driven mutations of human mitochondrial DNA.

Authors:  M Zeviani
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

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