Whitehouse D B, Abbott C M, Lovegrove J U, McIntosh I, McMahon C J, Mieli-Vergani G, Mowat A P, Hopkinson D A
MRC Human Biochemical Genetics Unit, Galton Laboratory, University College London.
J Med Genet. 1989 Dec;26(12):744-9. doi: 10.1136/jmg.26.12.744.
During a study of the alpha 1 antitrypsin (AAT) protein and its locus (PI) by high resolution isoelectric focusing and direct molecular analysis of 106 PIZ probands and their families, a new allele (Ztun) was identified that resembles Z in many of its properties. Two sibs, both compound heterozygotes for Ztun and Z, showed similar evidence of mild liver involvement that was indistinguishable from that associated with classical ZZ homozygotes. The Ztun protein appeared to be deficient in the plasma to about the same degree as the Z protein. Allele specific oligonucleotide analysis of amplified genomic DNA indicated that the new allele is the result of a mutation in exon V that is identical to the classical G----A transition at codon 342 that results in the Glu----Lys substitution characteristic of the Z allele. An analysis of DNA haplotypes constructed from polymorphic restriction enzyme recognition sites in and around the PI locus confirmed that Ztun probably represents a new mutation at codon 342 that has occurred on an M2-like genetic background.
在一项通过高分辨率等电聚焦和对106名PIZ先证者及其家系进行直接分子分析来研究α1抗胰蛋白酶(AAT)蛋白及其基因座(PI)的研究中,发现了一种新的等位基因(Ztun),其许多特性与Z相似。两名同胞,均为Ztun和Z的复合杂合子,表现出类似的轻度肝脏受累迹象,与经典的ZZ纯合子相关的表现无法区分。Ztun蛋白在血浆中的缺乏程度似乎与Z蛋白大致相同。对扩增的基因组DNA进行等位基因特异性寡核苷酸分析表明,新等位基因是外显子V中一个突变的结果,该突变与导致Z等位基因特征性Glu→Lys替代的密码子342处的经典G→A转换相同。对由PI基因座及其周围的多态性限制性酶识别位点构建的DNA单倍型的分析证实,Ztun可能代表在M2样遗传背景上密码子342处发生的一个新突变。