Yu L C, Lee H L, Chu C C, Broadberry R E, Lin M
Transfusion Medicine Laboratory, Department of Medical Research, Mackay Memorial Hospital, Taipei, Taiwan.
Vox Sang. 1999;76(2):115-9. doi: 10.1159/000031030.
The human Secretor alpha(1, 2)fucosyltransferase gene determines the ABH secretor status and influences the Lewis phenotype of an individual. Studies were carried out on the Lewis (a+b-) nonsecretors of different groups indigenous to Taiwan to demonstrate their se genotypes.
The Lewis phenotype of the blood samples was determined by a microplate method. The se genotypes of the individuals with the Lewis (a+b-) phenotype were analyzed by a polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP) method designed for the se alleles reported previously. PCR and cloning techniques were used to determine the coding sequence of the novel se gene.
A new se allele, se685, with a three-nucleotide deletion of GTGGT to GT in the coding region of nucleotides 685 through 689 was identified in a Le (a+b-) nonsecretor from the Ami tribe indigenous to Taiwan. The deletion predicts the loss of the amino acid Val230 in the corresponding secretor enzyme's C-terminal segment. The distribution of the se685 allele in the Ami tribe was further verified by PCR-RFLP analysis.
The Se gene exhibits heterogeneity with some Se alleles being common but others displaying a unique distribution in different ethnic populations. The newly identified se685 allele seems to exist only in the Ami tribe indigenous to Taiwan.
人类分泌型α(1,2)岩藻糖基转移酶基因决定ABH分泌状态,并影响个体的Lewis血型表型。对台湾不同原住民群体的Lewis(a+b-)非分泌型个体进行研究,以确定其se基因型。
采用微孔板法测定血样的Lewis血型表型。采用针对先前报道的se等位基因设计的聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法,分析Lewis(a+b-)表型个体的se基因型。运用PCR和克隆技术确定新se基因编码序列。
在台湾阿美族的一名Le(a+b-)非分泌型个体中,鉴定出一种新的se等位基因se685,其在核苷酸685至689的编码区有一个三核苷酸缺失,即从GTGGT缺失为GT。该缺失预测相应分泌酶C末端片段中氨基酸Val230的缺失。通过PCR-RFLP分析进一步验证了se685等位基因在阿美族中的分布。
Se基因表现出异质性,一些Se等位基因较为常见,而其他等位基因在不同种族人群中分布独特。新鉴定的se685等位基因似乎仅存在于台湾原住民阿美族中。