Human erythrocyte protein L-isoaspartyl methyltransferase: Heritability of basal activity and genetic polymorphism for thermal stability

Protein L-isoaspartyl methyltransferase (PIMT) is believed to play an important role in the disposition of age-damaged proteins by catalyzing the repair of abnormal isoaspartyl linkages resulting from the spontaneous deamidation of asparaginyl residues or isomerization of aspartyl residues, As a step toward testing the hypothesis that human disease-or age-related pathology might be associated with a deficiency in PIMT, we investigated basal activity and thermal stability of PIMT in erythrocyte lysates from 299 U.S. family members, Thermal stability was measured because it is a sensitive measure of variation in amino acid sequence, Basal activity was normally distributed with a mean +/- SD of 558 +/- 43 units/ml erythrocytes. Statistical analysis of the data revealed that basal PIMT activity exhibited a high degree of heritability. Enzyme thermal stability showed a skewed bimodall frequency distribution, and segregation analysis of family member pedigrees was consistent with Mendelian inheritance of two major alleles, No DNA was available from the family samples, so we tested two additional population samples for a known Ile/Val polymorphism at codon 119 and for PIMT activity and thermal stability, using blood donated by 25 Norwegians and by 20 Koreans, Single-stranded conformational polymorphism analysis using polymerase chain reaction revealed a 100% correlation between thermal stability grouping and this polymorphism, The high thermal stability samples were all homozygous ne, the low thermal stability samples were all homozygous Val, and the intermediate thermal stability samples were all heterozygous. Furthermore, this polymorphism was responsible, in part, for the variation observed in basal erythrocyte PIMT activity, These results will help provide a foundation for future studies aimed. It correlating levels of PIMT activity, or other properties of this enzyme, with human disease. (C) 1997 Academic Press.