An HLA-B null allele (B*1526N) with a stop codon in exon 3 generated by a point mutation

Tissue Antigens. 1997 Oct;50(4):351-4. doi: 10.1111/j.1399-0039.1997.tb02886.x.

Abstract

An HLA-B null allele was identified in a Japanese family during histocompatibility testing for bone marrow transplantation. The propositus was a healthy Japanese woman with three children, and her parents were cousins. Serological HLA typing of the family members indicated that the propositus was homozygous for the A24-Cw4-B blank (B null)-DR4.2-DQ3 haplotype. Total RNA was extracted from peripheral blood of the propositus was converted to first-strand cDNA using reverse transcriptase. The cDNA was amplified by the polymerase chain reaction (PCR) using HLA-B locus-specific primers. The PCR product showed no change in size upon polyacrylamide gel electrophoresis (PAGE) compared to that of normal controls, suggesting that HLA-B gene mRNA was normally expressed. The nucleotide sequence of the cDNA was the same as that of B*1501 except at nucleotide 369 or codon 123, where C was replaced with A; TAC encodes Tyr whereas TAA is a stop codon. This point mutation may have truncated the HLA-B molecule of the propositus, resulting in the negative results we obtained with anti-HLA-B sera.

Publication types

  • Comment

MeSH terms

  • Adult
  • Alleles*
  • Base Sequence
  • Codon / genetics*
  • Consanguinity
  • Consensus Sequence
  • DNA Mutational Analysis
  • DNA, Complementary / genetics
  • Exons / genetics*
  • Female
  • Genes, MHC Class I*
  • HLA-B Antigens / genetics*
  • Homozygote
  • Humans
  • Male
  • Molecular Sequence Data
  • Pedigree
  • Point Mutation*
  • Polymerase Chain Reaction
  • Sequence Alignment
  • Sequence Homology, Nucleic Acid
  • Terminator Regions, Genetic / genetics*

Substances

  • Codon
  • DNA, Complementary
  • HLA-B Antigens

Associated data

  • GENBANK/D49824