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Molecular genetic basis of the histo-blood group ABO system

NaturePublished 1 May 1990
Fumi-ichiro Yamamoto, Henrik Clausen, Thayer White, John Marken, Sen-itiroh Hakomori
Citations1,190
SJR quartileQ1
SJR score18.29
SNIP10.16

TL;DR

A critical single-base deletion was found in the 0 gene, which results in an entirely different, inactive protein incapable of modifying the H antigen, and this work presents a molecular basis for the ABO genotypes.

Abstract

The histo-blood group ABO, the major human alloantigen system, involves three carbohydrate antigens (ABH). A, B and AB individuals express glycosyltransferase activities converting the H antigen into A or B antigens, whereas O(H) individuals lack such activity. Here we present a molecular basis for the ABO genotypes. The A and B genes differ in a few single-base substitutions, changing four amino-acid residues that may cause differences in A and B transferase specificity. A critical single-base deletion was found in the O gene, which results in an entirely different, inactive protein incapable of modifying the H antigen.

Keywords

MedicineBiochemistry, Genetics and Molecular Biology