Molecular characterization of genetic mutation in human lactate dehydrogenase-A (M) deficiency

Biochem Biophys Res Commun. 1990 Apr 30;168(2):677-82. doi: 10.1016/0006-291x(90)92374-9.

Abstract

Human lactate dehydrogenase-A mutant gene was isolated from the genomic DNA library of a patient deficient in LDH-A (Muscle) subunit. The nucleotide sequences of seven protein-coding exons were determined and a deletion of 20 base-pairs in exon 6 was found. This mutation results in a frame-shift translation and premature termination. The predicted incomplete LDH-A (M) subunit containing only 259 instead of 331 amino acids appears to be degraded rapidly, since no protein was detected immunologically (Maekawa et al., Am J Hum Genet 39:232-238, 1986). In addition, three synonymous (silent) substitutions, A to C, T to C, and G to A, were observed at codons 115, 160 and 172, respectively, in this LDH-A mutant gene.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Base Sequence
  • DNA / isolation & purification
  • Exons
  • Female
  • Humans
  • L-Lactate Dehydrogenase / deficiency*
  • L-Lactate Dehydrogenase / genetics
  • Molecular Sequence Data
  • Mutation*
  • Restriction Mapping

Substances

  • DNA
  • L-Lactate Dehydrogenase