Breimer L H, Winder A F, Jay B, Jay M
Department of Chemical Pathology and Human Metabolism, Royal Free Hospital School of Medicine, London, UK.
Clin Chim Acta. 1994 Jun;227(1-2):17-22. doi: 10.1016/0009-8981(94)90131-7.
Direct DNA sequence determination of PCR amplified exons of the tyrosinase gene of three British patients suffering from tyrosinase negative oculocutaneous albinism has revealed three new missense point mutations: (1) an adenine to guanine transition at codon 1 changes the initiating methionine codon into a valine codon thereby abolishing translation; (2) a thymine to cytosine transition at codon 370 changes a methionine to a threonine residue; (3) a cytosine to thymine transition at codon 367 changes a histidine to a tyrosine residue. A codon 402 change previously considered a polymorphism is assigned a pathological role.
对三名患有酪氨酸酶阴性眼皮肤白化病的英国患者的酪氨酸酶基因PCR扩增外显子进行直接DNA序列测定,发现了三个新的错义点突变:(1)密码子1处的腺嘌呤到鸟嘌呤的转换将起始甲硫氨酸密码子变为缬氨酸密码子,从而使翻译终止;(2)密码子370处的胸腺嘧啶到胞嘧啶的转换将甲硫氨酸变为苏氨酸残基;(3)密码子367处的胞嘧啶到胸腺嘧啶的转换将组氨酸变为酪氨酸残基。先前被认为是多态性的密码子402变化被确定具有病理作用。