A novel Bweak hybrid allele lacks three enhancer repeats but generates normal ABO transcript levels

Authors

  • B. Thuresson,

    1. Division of Hematology and Transfusion Medicine, Department of Laboratory Medicine, Lund University, Lund, Sweden
    2. Department of Clinical Immunology and Transfusion Medicine, University and Regional Laboratories, Region Skåne, Sweden
    Search for more papers by this author
  • B. Hosseini-Maaf,

    1. Division of Hematology and Transfusion Medicine, Department of Laboratory Medicine, Lund University, Lund, Sweden
    2. Department of Clinical Immunology and Transfusion Medicine, University and Regional Laboratories, Region Skåne, Sweden
    Search for more papers by this author
  • A. K. Hult,

    1. Division of Hematology and Transfusion Medicine, Department of Laboratory Medicine, Lund University, Lund, Sweden
    2. Department of Clinical Immunology and Transfusion Medicine, University and Regional Laboratories, Region Skåne, Sweden
    Search for more papers by this author
  • H. Hustinx,

    1. The Blood Transfusion Service (Swiss Red Cross), Bern, Switzerland
    Search for more papers by this author
  • M. Alan Chester,

    1. Division of Hematology and Transfusion Medicine, Department of Laboratory Medicine, Lund University, Lund, Sweden
    Search for more papers by this author
  • M. L. Olsson

    1. Division of Hematology and Transfusion Medicine, Department of Laboratory Medicine, Lund University, Lund, Sweden
    2. Department of Clinical Immunology and Transfusion Medicine, University and Regional Laboratories, Region Skåne, Sweden
    Search for more papers by this author

Martin L. Olsson, Blood Centre, University Hospital, S-221 85 Lund, Sweden
E-mail: Martin_L.Olsson@med.lu.se

Abstract

Background and Objectives  Weak expression of A/B histo-blood group antigens is often explained by single nucleotide substitutions at the ABO locus. However, hybrid alleles containing segments from different ABO alleles can result in unexpected phenotypes and may complicate genotype analysis. We investigated the basis of weak B phenotype in a referred sample.

Materials and Methods  A healthy young woman was serologically phenotyped as ABweak and RBCs were characterized by flow cytometry. All seven ABO exons, five introns plus the 5′-region including the CCAAT-binding factor/Nuclear Factor Y (CBF/NF-Y) binding enhancer were sequenced. ABO transcript levels were measured in fresh peripheral blood samples. Expression of B antigen was semiquantified following transfection of HeLa cells.

Results  A new Bweak allele with 53G>T resulted in a characteristic pattern of moderately weakened B antigen expression on RBCs. Its sequence revealed a novel hybrid between O2 [O03] and B [B101] alleles with a crossingover region in intron 4 as defined by allele-specific polymorphisms. B transcript levels were similar to normal controls despite the O2-related single CBF/NF-Y-binding 43-bp motif in the enhancer region. Expression of the glycosyltransferase including the O2-specific Arg18Leu substitution resulted in a slight decrease in B-antigen-positive cells.

Conclusion  We describe here the first hybrid between an O2 and a B allele and characterized the associated decrease in B antigen expression. Although it lacks three enhancer repeat units compared to common B alleles, the resulting transcript level was unaltered. This study challenges previous suggestions that the number of 43-bp motifs in the ABO enhancer determines transcription rates in erythroid cells.

Ancillary