Literature DB >> 9876894

A protocol for detection of mitochondrial DNA deletions: characterization of a novel deletion.

M B Coulter-Mackie1, D A Applegarth, J R Toone, L Gagnier.   

Abstract

OBJECTIVES: To develop a protocol capable of identifying deletions in mitochondrial DNA and use it to identify the breakpoints of a mtDNA deletion in a patient with chronic progressive external ophthalmoplegia (CPEO). DESIGN AND METHODS: Deletions in mtDNA were identified by a combination of long range PCR and Southern blotting. The precise breakpoints were determined by automated DNA sequencing.
RESULTS: A series of DNA samples from patients with suspected mitochondrial disease was subjected to a protocol, which combines long range PCR and Southern blotting. We found a unique deletion in a patient with CPEO and we identified the precise location of this deletion through DNA sequencing.
CONCLUSIONS: Long range PCR has the advantages of speed, minimal samples requirements, and sensitivity. Southern blotting is better able to evaluate heteroplasmy and detect duplications. We suggest a protocol that enables us to identify precisely the breakpoints in a unique mutation of mtDNA in a patient with CPEO.

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Year:  1998        PMID: 9876894     DOI: 10.1016/s0009-9120(98)00074-5

Source DB:  PubMed          Journal:  Clin Biochem        ISSN: 0009-9120            Impact factor:   3.281


  5 in total

Review 1.  Chronic progressive external ophthalmoplegia.

Authors:  Andrew G Lee; Paul W Brazis
Journal:  Curr Neurol Neurosci Rep       Date:  2002-09       Impact factor: 5.081

2.  A rare case report of simultaneous presentation of myopathy, Addison's disease, primary hypoparathyroidism, and Fanconi syndrome in a child diagnosed with Kearns-Sayre syndrome.

Authors:  Meropi Tzoufi; Alexandros Makis; Nikolaos Chaliasos; Iliada Nakou; Ekaterini Siomou; Agathoklis Tsatsoulis; Anastasia Zikou; Maria Argyropoulou; Jean Paul Bonnefont; Antigone Siamopoulou
Journal:  Eur J Pediatr       Date:  2012-08-09       Impact factor: 3.183

3.  Mutation in the mitochondrial tRNA(Val) causes mitochondrial encephalopathy, lactic acidosis and stroke-like episodes.

Authors:  Catherine Glatz; Kristin D'Aco; Sabrina Smith; Neal Sondheimer
Journal:  Mitochondrion       Date:  2011-04-20       Impact factor: 4.160

4.  FASTKD2 nonsense mutation in an infantile mitochondrial encephalomyopathy associated with cytochrome c oxidase deficiency.

Authors:  Daniele Ghezzi; Ann Saada; Pio D'Adamo; Erika Fernandez-Vizarra; Paolo Gasparini; Valeria Tiranti; Orly Elpeleg; Massimo Zeviani
Journal:  Am J Hum Genet       Date:  2008-09-04       Impact factor: 11.025

5.  Generation and Evaluation of Isogenic iPSC as a Source of Cell Replacement Therapies in Patients with Kearns Sayre Syndrome.

Authors:  Glen Lester Sequiera; Abhay Srivastava; Keshav Narayan Alagarsamy; Cheryl Rockman-Greenberg; Sanjiv Dhingra
Journal:  Cells       Date:  2021-03-05       Impact factor: 6.600

  5 in total

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