Molecular characterization of gene expression in human lactate dehydrogenase-A deficiency

Neurology. 1993 Jul;43(7):1414-9. doi: 10.1212/wnl.43.7.1414.

Abstract

Recurrent rhabdomyolysis due to decreased glycolysis occurred during strenuous exercise in patients with lactate dehydrogenase-A-subunit (LDH-A; muscle) deficiency. Enzyme activities of LDH in the muscle were decreased less than 8% of the control value. The isozyme pattern revealed only one band of B4. The level of LDH-A mRNA was not decreased. The direct sequencing of the reverse transcription-polymerase chain reaction product that corresponds to exon 6 revealed a deletion of 20 nucleotides. Immunofluorescence staining showed the presence of LDH-A protein within the cytoplasm. These findings suggest that an incomplete LDH-A protein lacking the subunit contact subdomain could not assemble into a tetrameric structure that has an enzymatic activity.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Amino Acid Sequence
  • Base Sequence
  • Blotting, Northern
  • Female
  • Fluorescent Antibody Technique
  • Gene Expression*
  • Humans
  • Immunohistochemistry
  • Isoenzymes
  • L-Lactate Dehydrogenase / deficiency
  • L-Lactate Dehydrogenase / genetics*
  • Molecular Sequence Data
  • Muscles / enzymology*
  • Oligonucleotide Probes
  • Polymerase Chain Reaction
  • RNA, Messenger / genetics
  • Transcription, Genetic

Substances

  • Isoenzymes
  • Oligonucleotide Probes
  • RNA, Messenger
  • L-Lactate Dehydrogenase