Multiplex ligation-dependent probe amplification (MLPA) assay for the detection of mitochondrial DNA deletion in chronic progressive external ophthalmoplegia (CPEO)

Ann Clin Lab Sci. 2011 Fall;41(4):385-9.

Abstract

Chronic progressive external ophthalmoplegia (CPEO) is a mitochondrial myopathy commonly caused by deleterious changes in the mitochondrial DNA (mtDNA). We describe a 45-year-old man who was referred to us for investigation of progressive ptosis. We performed a multiplex ligation-dependent probe amplification (MLPA) assay of mtDNA from muscle tissue and peripheral blood leukocytes, and followed up with gap-polymerase chain reaction (PCR) and direct sequence analysis. Results showed a deletion of a 4,407 bp segment in the mtDNA region, ranging from nucleotide position 8,577 in the MT-ATP6 gene to nucleotide position 12,983 in the MT-ND5 gene. To the best of our knowledge, this is the first report of a CPEO patient with a large novel deletion of mtDNA genetically confirmed by MLPA assay. MLPA can be a feasible platform for clinical laboratories to detect large deletion mutations in the mtDNA for suspected cases.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Biological Assay / methods*
  • DNA Probes / metabolism*
  • DNA, Mitochondrial / genetics*
  • Gene Dosage / genetics
  • Humans
  • Male
  • Middle Aged
  • Molecular Sequence Data
  • Multiplex Polymerase Chain Reaction / methods*
  • Ophthalmoplegia, Chronic Progressive External / genetics*
  • Sequence Deletion / genetics*

Substances

  • DNA Probes
  • DNA, Mitochondrial