Henry S, Mollicone R, Lowe J B, Samuelsson B, Larson G
Department of Clinical Chemistry and Transfusion Medicine, Göteborg University, Sweden.
Vox Sang. 1996;70(1):21-5. doi: 10.1111/j.1423-0410.1996.tb00991.x.
While screening Le(a+b+)Polynesian DNA samples for a candidate Se(w) allele, a point mutation (C571-->T) resulting in a new stop codon (Arg191-->stop) in the alpha(1,2)fucosyltransferase gene (FUT2) was identified. This point mutation resulted in the gaining of a new restriction enzyme cleavage site (DdeI), which allowed restriction enzyme cleavage screening of 40 selected Polynesians and 42 random Caucasians. The nonsecretor phenotype in two of the three nonsecretor Polynesians analyzed was due to homozygosity for the 'new' mutation, whereas the third Polynesian nonsecretor (with Caucasian ancestors) was due to homozygosity of the 'old' (Trp143-->stop) mutation. The nonsecretor phenotype in all Caucasians analyzed was a consequence of homozygosity for the 'old' mutation. Both the new and the old nonsecretor mutations were identified in the heterozygous state in some secretor-positive Polynesians, while only the old mutation was found in the heterozygous state in Caucasians of the same phenotype.
在筛选Le(a+b+)波利尼西亚人DNA样本以寻找候选Se(w)等位基因时,在α(1,2)岩藻糖基转移酶基因(FUT2)中发现了一个点突变(C571→T),该突变导致产生一个新的终止密码子(Arg191→终止)。这个点突变产生了一个新的限制性内切酶切割位点(DdeI),这使得能够对40名选定的波利尼西亚人和42名随机选择的高加索人进行限制性内切酶切割筛选。在分析的三名非分泌型波利尼西亚人中,有两人的非分泌型表型是由于对“新”突变的纯合性,而第三名波利尼西亚非分泌型(有高加索人祖先)是由于“旧”(Trp143→终止)突变的纯合性。在所有分析的高加索人中,非分泌型表型是“旧”突变纯合性的结果。在一些分泌型阳性的波利尼西亚人中,新的和旧的非分泌型突变均以杂合状态被鉴定出来,而在相同表型的高加索人中,仅发现旧突变以杂合状态存在。