The recombinant HLA-B5518 allele supports the evidence of conserved haplotype association of rare alleles

• Published in: Tissue antigens 2005-08, Vol.66 (2), p.156-159
• Main Authors: Lebedeva, T.V., Huang, A., Ohashi, M., Sibilia, P., Alosco, S.M., Kempenich, J., Yu, N.
• Format: Article
• Language: English
• Subjects: Alleles; Amino Acid Sequence; Base Sequence; Genotype; Guam; Haplotypes; HLA; HLA-B Antigens - genetics; HLA-B Antigens - immunology; Humans; Molecular Sequence Data; polymorphism; Polymorphism, Single Nucleotide; Recombination, Genetic; Sequence Homology, Nucleic Acid; sequence-based typing; Tissue Donors
• ISSN: 0001-2815; 1399-0039
• DOI: 10.1111/j.1399-0039.2005.00442.x

:  Allelic polymorphism of the major histocompatibility complex arises mostly from gene recombination. Intralocus gene recombination usually involves short fragments of DNA leading most commonly to single‐nucleotide substitutions and rarely involves large fragments. Here, we report a new recombinant human leukocyte antigen (HLA)‐B*5518 allele that has arisen via recombination of a large fragment of DNA spanning more than 70 nucleotides. During routine HLA typing of potential volunteer donors for the National Marrow Donor Program®, a new HLA‐B allele was identified in two donors from Guam. The allele, B*5518, appears to be a product of recombination between B*5502 and B*40. Exons 1, 3, and 4 of the new allele belong to B*5502, whereas part of exon 2 belongs to one of B*40 alleles. Introns 1 and 2 appear to belong to B*55, suggesting that the recombination event may have occurred within the homologous parts of exon 2.