Hidaka Y, Tarlé S A, Fujimori S, Kamatani N, Kelley W N, Palella T D
Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor 48109.
J Clin Invest. 1988 Mar;81(3):945-50. doi: 10.1172/JCI113408.
Complete adenine phosphoribosyltransferase (APRT) deficiency causes 2,8-dihydroxyadenine urolithiasis. In previous reports, analysis of the kinetic properties of APRT from APRT-deficient Japanese subjects revealed strikingly similar abnormalities suggesting a distinct "Japanese-type" mutation. In this paper, we report studies of 11 APRT-deficient lymphoblast cell lines. Nucleotide sequence analysis of APRT genomic DNA from WR2, a Japanese-type homozygote, identified a T to C substitution in exon 5, giving rise to the substitution of threonine for methionine at position 136. RNase mapping analysis confirmed this mutation in WR2 and revealed that six other Japanese-type homozygotes carry the same mutation on at least one allele. The remaining Japanese subject, who does not express the Japanese-type phenotype, did not demonstrate this mutation. Southern blot analysis showed that all seven Japanese-type subjects were confined to one TaqI restriction fragment length polymorphism (RFLP) haplotype. These studies provide direct evidence for the nature of the mutation in the Japanese-type APRT deficiency.
腺嘌呤磷酸核糖转移酶(APRT)完全缺乏会导致2,8 - 二羟基腺嘌呤尿路结石。在先前的报告中,对来自APRT缺乏的日本受试者的APRT动力学特性分析显示出惊人相似的异常,提示存在一种独特的“日本型”突变。在本文中,我们报告了对11个APRT缺乏的淋巴母细胞系的研究。对日本型纯合子WR2的APRT基因组DNA进行核苷酸序列分析,发现在外显子5中有一个T到C的替换,导致第136位的苏氨酸替代甲硫氨酸。核糖核酸酶图谱分析证实了WR2中的这种突变,并显示其他六个日本型纯合子至少在一个等位基因上携带相同的突变。其余未表现出日本型表型的日本受试者未显示出这种突变。Southern印迹分析表明,所有七个日本型受试者都局限于一种TaqI限制性片段长度多态性(RFLP)单倍型。这些研究为日本型APRT缺乏症突变的性质提供了直接证据。