A novel cisAB allele with a missense variant (c.971T>C) in the ABO gene of a Brazilian family

Vox Sang. 2024 Nov;119(11):1196-1200. doi: 10.1111/vox.13727. Epub 2024 Aug 20.

Abstract

Background and objectives: Missense variants in exon 7 of the ABO gene can lead to the formation of cisAB alleles. These alleles encode glycosyltransferases (GTs) capable of synthesizing both A and B antigens. In this study, we report the discovery of a novel cisAB allele and characterize it at molecular, protein and serological levels.

Materials and methods: Blood and DNA samples from the proband and seven relatives were examined using standard and modified ABO phenotyping, polymerase chain reaction-restriction fragment length polymorphism and ABO gene sequencing. We assessed the impact of the p.Leu324Ser variant on the protein structure of the mutant GT using bioinformatics tools.

Results: Molecular tests revealed a c.971T>C (p.Leu324Ser) variant in the ABO gene in five of the eight individuals. This variant results in a GT that produces more A antigens and fewer B antigens. Bioinformatics analysis suggests that the amino acid substitution (p.Leu324Ser) could potentially affect enzymatic activity and specificity of the GT.

Conclusion: We identified a novel cisAB allele resulting from a c.971T>C variant in the ABO gene. This variant led to the expression of an ABweak phenotype.

Keywords: ABO blood group; ABO genotyping; cisAB allele.

MeSH terms

  • ABO Blood-Group System* / genetics
  • Adult
  • Alleles*
  • Amino Acid Substitution
  • Brazil
  • Female
  • Glycosyltransferases / genetics
  • Humans
  • Male
  • Mutation, Missense*

Substances

  • ABO Blood-Group System
  • Glycosyltransferases