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人类组织血型α(1,2)岩藻糖基转移酶基因(FUT2)新鉴定出的一种非分泌型等位基因。

A newly identified nonsecretor allele of the human histo-blood group alpha(1,2)fucosyltransferase gene (FUT2).

作者信息

Yu L C, Lee H L, Chu C C, Broadberry R E, Lin M

机构信息

Transfusion Medicine Laboratory, Department of Medical Research, Mackay Memorial Hospital, Taipei, Taiwan.

出版信息

Vox Sang. 1999;76(2):115-9. doi: 10.1159/000031030.

Abstract

BACKGROUND AND OBJECTIVES

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.

METHODS

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.

RESULTS

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.

CONCLUSION

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.

摘要

背景与目的

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。

方法

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。

结果

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。

结论

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。

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