A novel allele of FUT2 gene containing a deletion of nine bases (c.461_469delGGACCTTCT) in a Chinese Han blood donor.

Autor: Zhou, Shihang, Wang, Liying, Song, Wenqian, Xia, Yuexin, Shao, Linnan, Liang, Xiaohua
Předmět:
Zdroj: Vox Sanguinis; Nov2023, Vol. 118 Issue 11, p988-992, 5p
Abstrakt: Background and Objectives: The FUT2 gene is responsible for the synthesis of the H antigen in body secretions. It is highly polymorphic and population specific. We investigated the FUT2 gene polymorphism in Chinese blood donors and found a novel deletion mutation in one non‐secretor individual. This study aimed to identify mutation(s) responsible for a non‐secretor phenotype. Materials and Methods: The Lewis blood group of a Chinese Han blood donor was typed using the standard serological technique and the FUT2 gene of the sample was analysed by Sanger sequencing. Clone sequencing was performed for determining the haplotype of the FUT2 gene. Bioinformatics tools were used for predicting the effect of the deletion on the FUT2 gene. Results: A novel nine‐base deletion (c.461_469delGGACCTTCT) in the FUT2 gene was identified in a Chinese Han blood donor. Two haplotypes Se390,418 and se204,249,461_469del,772,993 were determined by clone sequencing. According to the prediction of bioinformatics tools, the mutation at c.461_469delGGACCTTCT might not influence the activity of the Se enzyme. Conclusion: We identified a new FUT2 mutation, the deletion of nine bases (c.461_469delGGACCTTCT), in a Chinese Han blood donor. This deletion was reported for the first time. [ABSTRACT FROM AUTHOR]
Databáze: Complementary Index
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