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

M Maekawa, K Sudo, T Kanno, SSL Li - Biochemical and biophysical …, 1990 - Elsevier
M Maekawa, K Sudo, T Kanno, SSL Li
Biochemical and biophysical research communications, 1990Elsevier
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 frameshift 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 …
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 frameshift 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.
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