Objective: To study the serological characteristics and molecular biological basis of 8 individuals with Para-Bombay phenotypes in Guangxi area.
Methods: Serological tests were used to identify the blood groups of red cells. Molecular biological methods, including PCR-SSP for ABO genotyping and DNA sequencing for FUT1, were used to detect the genotypes of ABO and FUT1 which determined the expression of H antigen.
Results: Eight individuals in the study were all the Para-Bombay phenotypes, including 4 cases of Bmh and 4 cases of Amh. The DNA sequencing for FUT1 showed that 6 cases were h3h3 [c.658C>T (p.Arg220Cys) homozygous mutation], 1 was h832h832 [c.832G>A (p.Asp278Asn) homozygous mutation], and 1 was h328h3 [compound heterozygous mutations of c.328G>A (p.Ala110Thr) and c.658C>T (p.Arg220Cys)].
Conclusion: There are varieties of molecular genetic mechanisms for Para-Bombay phenotypes. In this study, the FUT1 mutations that cause Para-Bombay phenotypes in Guangxi area are mainly h3, h328, and h832, among which h3 is the most common mutant.
题目: 广西地区8例类孟买血型个体的血清学鉴定及FUT1基因突变分析.
目的: 对广西地区8例类孟买血型个体进行血清学及分子生物学背景分析。.
方法: 采用血型血清学方法对研究标本进行血型鉴定,用分子生物学方法进行基因型分析,包括以PCR-SSP方法进行ABO基因分型和测序,对决定H抗原表达的FUT1基因进行分析。.
结果: 8例类孟买血型中,4例为Bmh,4例为Amh。FUT1基因测序结果显示,6例为h3h3突变[c.658C>T(p.Arg220Cys)突变纯合子],1例为h832h832突变[c.832G>A(p.Asp278Asn)突变纯合子],1例为h328h3突变[c.328G>A(p.Ala110Thr)突变杂合子合并c.658C>T(p.Arg220Cys)突变杂合子]。.
结论: 类孟买血型存在多种分子遗传机制,在本研究中,广西地区类孟买血型个体中发现导致类孟买血型的FUT1基因突变主要包括h3、h328和h832 3种,其中以h3突变最多见。.