David C L, Szumlanski C L, DeVry C G, Park-Hah J O, Clarke S, Weinshilboum R M, Aswad D W
Department of Molecular Biology and Biochemistry, University of California, Irvine 92697-3900, USA.
Arch Biochem Biophys. 1997 Oct 15;346(2):277-86. doi: 10.1006/abbi.1997.0303.
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 bimodal 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 Ile, 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 at correlating levels of PIMT activity, or other properties of this enzyme, with human disease.
蛋白质L-异天冬氨酰甲基转移酶(PIMT)被认为在处理老化受损蛋白质过程中发挥重要作用,它通过催化修复由天冬酰胺残基的自发脱酰胺作用或天冬氨酸残基的异构化作用所产生的异常异天冬氨酰连接。作为检验人类疾病或与年龄相关的病理学可能与PIMT缺乏有关这一假说的一个步骤,我们研究了299名美国家庭成员红细胞裂解物中PIMT的基础活性和热稳定性。之所以测量热稳定性,是因为它是氨基酸序列变异的一个敏感指标。基础活性呈正态分布,红细胞中平均±标准差为558±43单位/毫升。数据的统计分析表明,基础PIMT活性具有高度遗传性。酶的热稳定性呈现出偏态双峰频率分布,家庭成员谱系的分离分析与两个主要等位基因的孟德尔遗传一致。由于没有来自家庭样本的DNA,因此我们使用25名挪威人和20名韩国人捐献的血液,对另外两个群体样本进行了密码子119处已知的异亮氨酸/缬氨酸多态性以及PIMT活性和热稳定性的检测。使用聚合酶链反应的单链构象多态性分析显示,热稳定性分组与这种多态性之间存在100%的相关性。高热稳定性样本均为纯合异亮氨酸,低热稳定性样本均为纯合缬氨酸,中等热稳定性样本均为杂合子。此外,这种多态性部分导致了基础红细胞PIMT活性中观察到的变异。这些结果将有助于为今后旨在将PIMT活性水平或该酶的其他特性与人类疾病相关联的研究奠定基础。