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Probable biosynthetic pathway for the synthesis of the B antigen for Bh variants.

Authors
  • Mulet, C
  • Cartron, J P
  • Schenkel-Brunner, H
  • Duchet, D
  • Sinay, P
  • Salmon, C
Type
Published Article
Journal
Vox sanguinis
Publication Date
Jan 01, 1979
Volume
37
Issue
5
Pages
272–280
Identifiers
PMID: 118582
Source
Medline
License
Unknown

Abstract

Red cells and serum from two Bh variants (B+H-cells) have been investigated for B and H blood group glycosyltransferases. The H enzyme could not be detected using either type 1 or type 2 chain acceptors. The B enzyme was present in normal amount when 2'-fucosyllactose was used as substrate, neither 6'-fucosyllactose nor 6'-fucosyllactosamine could act as acceptors for the B enzyme. Upon treatment of the Bh red cells by the B-degrading enzyme from Trichomonas foetus the B antigen was destroyed while H determinants were uncovered (B-H + cells). The cells thus treated could be further converted into A&H-red cells by the action of the A transferase from human blood group A serum. Previous treatment of the B-H + cells by the H-degrading enzyme from T. foetus, however, led to B-/-erythrocytes and prevented their conversion into A red blood cells by the A enzyme. The results clearly demonstrate that, as found in normal B individuals, the B antigen from Bh cells is built up from the H precursor and provide additional evidence that H is not a completely silent gene in Bh individuals.

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