Tripathi R K, Giebel L B, Strunk K M, Spritz R A
Department of Medical Genetics, University of Wisconsin, Madison 53706.
Gene Expr. 1991 May;1(2):103-10.
We have identified a common nonpathological polymorphism of the human tyrosinase gene. In Caucasians codon 402 can be either CGA (arginine) [p = .85] or CAA (glutamine) [p = .15]. This polymorphism also occurs in American Blacks, but the codon 402CAA (Gln) allele was not detected in Oriental populations. The substitution of glutamine for arginine at codon 402 results in moderate thermoinstability of the corresponding tyrosinase polypeptide. Tyrosinase enzymatic activity expressed in HeLa cells transfected with a codon 402Gln tyrosinase cDNA is reduced by approximately 75 percent when cells are cultured at 37 degrees C as compared to 31 degrees C, whereas enzymatic activity of codon 402Arg tyrosinase is not temperature-sensitive. However, the genotype at codon 402 of tryosinase is not correlated with the apparent pigmentation phenotype in normal Caucasians.
我们已经鉴定出人类酪氨酸酶基因的一种常见非病理性多态性。在白种人中,密码子402可以是CGA(精氨酸)[p = 0.85]或CAA(谷氨酰胺)[p = 0.15]。这种多态性也存在于美国黑人中,但在东方人群中未检测到密码子402CAA(Gln)等位基因。密码子402处的谷氨酰胺取代精氨酸会导致相应酪氨酸酶多肽出现中度热不稳定性。当在37℃培养细胞时,与在31℃培养相比,用密码子402Gln酪氨酸酶cDNA转染的HeLa细胞中表达的酪氨酸酶酶活性降低约75%,而密码子402Arg酪氨酸酶的酶活性对温度不敏感。然而,在正常白种人中,酪氨酸酶密码子402的基因型与明显的色素沉着表型无关。