Bettens F, Tiercy J M
Transplantation Immunology Unit, University Hospital, Geneva, Switzerland.
Tissue Antigens. 2000 Nov;56(5):441-5. doi: 10.1034/j.1399-0039.2000.560507.x.
A new HLA class I null allele has been identified within the B44 group by combined serological and molecular typing of a blood donor. Based on full-length cDNA sequencing, this novel HLA-B4419N allele was found to differ from B4402 by one single base pair deletion at position 7 of exon 1 which results in a stop at codon 19. This mutation was confirmed by polymerace chain reaction-sequence-specific oligonucleotide probe (PCR-SSOP) hybridization on genomic DNA. Based on family typing, this new allele segregates with the haplotype A01-B4419N-Cw0501-DRB11301-DRB30101. Since nonsense codons are generally associated with increased mRNA decay, we investigated B4419N mRNA by semi-quantitative reverse transcriptase (RT)-PCR and by cDNA cloning efficiency. Comparison of B4419N cDNA to B4402 control cDNA and to B35 cDNA levels in the same donor, as well as the analysis of cloned inserts, revealed that the exon 1 mutation did not significantly influence B*4419N steady-state mRNA.