Literature DB >> 9309691

Detection of mitochondrial DNA deletions by a screening procedure using the polymerase chain reaction.

T Ferlin1, G Guironnet, M C Barnoux, R Dumoulin, G Stepien, B Mousson.   

Abstract

We describe an accurate procedure for a rapid diagnosis of heteroplasmic mtDNA deletions based on the polymerase chain reaction (PCR). For a selective amplification of deleted mtDNA across the breakpoints of the deletion, we used seven combinations of primers surrounding the most common deleted region between the two origins of mtDNA replication. This procedure was performed on muscle biopsies of twenty patients harboring a single mtDNA deletion and one patient with multiple mtDNA deletions. The results were compared with Southern-blotting analysis. We conclude that this PCR procedure is a sensitive and convenient screening method for the detection of mtDNA deletions.

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Year:  1997        PMID: 9309691

Source DB:  PubMed          Journal:  Mol Cell Biochem        ISSN: 0300-8177            Impact factor:   3.396


  21 in total

1.  Tandem direct duplications of mitochondrial DNA in mitochondrial myopathy: analysis of nucleotide sequence and tissue distribution.

Authors:  J Poulton; M E Deadman; R M Gardiner
Journal:  Nucleic Acids Res       Date:  1989-12-25       Impact factor: 16.971

2.  Mitochondrial DNA deletion in Pearson's marrow/pancreas syndrome.

Authors:  A Rotig; M Colonna; J P Bonnefont; S Blanche; A Fischer; J M Saudubray; A Munnich
Journal:  Lancet       Date:  1989-04-22       Impact factor: 79.321

3.  Juvenile Pearson syndrome.

Authors:  M E Blaw; C E Mize
Journal:  J Child Neurol       Date:  1990-07       Impact factor: 1.987

4.  Maternally transmitted partial direct tandem duplication of mitochondrial DNA associated with diabetes mellitus.

Authors:  D R Dunbar; P A Moonie; R J Swingler; D Davidson; R Roberts; I J Holt
Journal:  Hum Mol Genet       Date:  1993-10       Impact factor: 6.150

5.  Mitochondrial diabetes revisited.

Authors:  S W Ballinger; J M Shoffner; S Gebhart; D A Koontz; D C Wallace
Journal:  Nat Genet       Date:  1994-08       Impact factor: 38.330

6.  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

7.  Shuttling of integrated vectors from mammalian cells to E. coli is mediated by head-to-tail multimeric inserts.

Authors:  G Lutfalla; H Blanc; R Bertolotti
Journal:  Somat Cell Mol Genet       Date:  1985-05

8.  Maternally inherited duplication of the mitochondrial genome in a syndrome of proximal tubulopathy, diabetes mellitus, and cerebellar ataxia.

Authors:  A Rötig; J L Bessis; N Romero; V Cormier; J M Saudubray; P Narcy; G Lenoir; P Rustin; A Munnich
Journal:  Am J Hum Genet       Date:  1992-02       Impact factor: 11.025

9.  Spectrum of mitochondrial DNA rearrangements in the Pearson marrow-pancreas syndrome.

Authors:  A Rötig; T Bourgeron; D Chretien; P Rustin; A Munnich
Journal:  Hum Mol Genet       Date:  1995-08       Impact factor: 6.150

10.  Are duplications of mitochondrial DNA characteristic of Kearns-Sayre syndrome?

Authors:  J Poulton; K J Morten; K Weber; G K Brown; L Bindoff
Journal:  Hum Mol Genet       Date:  1994-06       Impact factor: 6.150

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  4 in total

1.  A novel variation in the Twinkle linker region causing late-onset dementia.

Authors:  Andoni Echaniz-Laguna; Jean-Baptiste Chanson; Jean-Marie Wilhelm; François Sellal; Martine Mayençon; Michel Mohr; Christine Tranchant; Bénédicte Mousson de Camaret
Journal:  Neurogenetics       Date:  2009-06-10       Impact factor: 2.660

2.  Expression of oxidative phosphorylation genes in muscle cell cultures from patients with mitochondrial myopathies.

Authors:  J M Collombet; H Faure-Vigny; G Mandon; R Dumoulin; S Boissier; A Bernard; B Mousson; G Stepien
Journal:  Mol Cell Biochem       Date:  1997-03       Impact factor: 3.396

3.  Large mitochondrial DNA deletion in an infant with addison disease.

Authors:  Gloria P Duran; A Martinez-Aguayo; H Poggi; M Lagos; D Gutierrez; P R Harris
Journal:  JIMD Rep       Date:  2011-09-22

4.  Identification of rare DNA variants in mitochondrial disorders with improved array-based sequencing.

Authors:  Wenyi Wang; Peidong Shen; Sreedevi Thiyagarajan; Shengrong Lin; Curtis Palm; Rita Horvath; Thomas Klopstock; David Cutler; Lynn Pique; Iris Schrijver; Ronald W Davis; Michael Mindrinos; Terence P Speed; Curt Scharfe
Journal:  Nucleic Acids Res       Date:  2010-09-15       Impact factor: 16.971

  4 in total

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