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[ABO血型CisAB亚型个体的分子基础]

[Molecular basis of an individual with CisAB subtype of ABO blood group].

作者信息

Li Haoru, Yang Jie, Chen Yanlin, Fu Haijun, Jin Xiuguo

机构信息

Blood Station of Zhoushan, Zhoushan, Zhejiang 316000, China.

出版信息

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Oct 10;35(5):741-743. doi: 10.3760/cma.j.issn.1003-9406.2018.05.028.

Abstract

OBJECTIVE

To explore the molecular basis for an individual with CisAB subtype of the ABO blood group.

METHODS

ABO antigen and serum antibody of the proband were detected with a serological method. Exons 5 to 7 of the ABO gene were amplified with PCR and sequenced bidirectionally. Allele-specific amplification for exon 6 to 7 was also carried out.

RESULTS

The proband was assigned as a CisAB phenotype based on his serological characteristics. Heterozygous variations including 220C/T, 261G/del, 297A/G, 467C/T, 646A/T, 681A/G, 771C/T, 803G/C, 829A/G and 1009A/G of the ABO gene were identified through direct sequencing, which was assigned as CisAB01var/O02 genotype. Allele-specific amplification indicated that the proband carried an O02 allele and a CisAB01var allele. Compared with A102, the CisAB01var allele has two nucleotide substitutions at 803G>C and 1009A>G, which resulted in replacement of amino acid Gly by Ala at position 268 and Arg by Gly at position 337.

CONCLUSION

The CisAB subtype was identified with 803G>C and 1009A>G variants in the α1,3-N-acetyl-galactosaminyltransferase gene compared with that of the A102 allele.

摘要

目的

探讨ABO血型CisAB亚型个体的分子基础。

方法

采用血清学方法检测先证者的ABO抗原和血清抗体。用聚合酶链反应(PCR)扩增ABO基因的第5至7外显子并进行双向测序。同时对外显子6至7进行等位基因特异性扩增。

结果

根据先证者的血清学特征确定其为CisAB表型。通过直接测序鉴定出ABO基因的杂合变异,包括220C/T、261G/del、297A/G、467C/T、646A/T、681A/G、771C/T、803G/C、829A/G和1009A/G,其被指定为CisAB01var/O02基因型。等位基因特异性扩增表明先证者携带一个O02等位基因和一个CisAB01var等位基因。与A102相比,CisAB01var等位基因在803G>C和1009A>G处有两个核苷酸替换,导致第268位氨基酸由甘氨酸被丙氨酸取代,第337位氨基酸由精氨酸被甘氨酸取代。

结论

与A102等位基因相比,在α1,3-N-乙酰半乳糖胺基转移酶基因中发现803G>C和1009A>G变异可鉴定CisAB亚型。

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