Hurley C K, Steiner N, Hoyer R J, Menchaca E, Mitton W, Simonis T, Hartzman R J, Johnson A H, Ng J
Department of Microbiology and Immunology, Georgetown University Medical School, Washington, DC, USA.
Tissue Antigens. 1996 Mar;47(3):179-87. doi: 10.1111/j.1399-0039.1996.tb02538.x.
Three class I alleles, B8201, B3515 and B5106, have been described using DNA and cDNA sequencing. The B8201 allele is most structurally related to B5602, differing from it by 14 nucleotide substitutions resulting in 5 amino acid differences. The other two alleles, B3515 and B5106, differ from their most closely related HLA-B alleles by 2-3 nucleotide substitutions resulting in 1-2 amino acid substitutions, respectively. The majority of nucleotide substitutions marking these new alleles are observed in other HLA-B alleles suggesting that gene conversion and/or reciprocal recombination have created this diversity. All of the amino acid substitutions are predicted to alter the antigen binding site of the HLA-B molecule. The newly defined HLA-B allelic products were originally defined by their unusual serologic reactivity patterns. The B8201 allelic product is serologically typed as a B "blank" or as a variant of B22 or B45. These patterns and the serologic reactivity of the other newly described allelic products are consistent with the protein sequence homology among specific HLA-B molecules. While serology remains a powerful tool for detecting HLA diversity, alleles generated by events resulting in the sharing of HLA sequence polymorphisms among alleles at a locus will continue to create complexity in the interpretation of typing results.
已通过DNA和cDNA测序鉴定出三个I类等位基因,即B8201、B3515和B5106。B8201等位基因在结构上与B5602最为相关,二者有14个核苷酸替换,导致5个氨基酸差异。另外两个等位基因,B3515和B5106,与其最密切相关的HLA - B等位基因分别有2 - 3个核苷酸替换,导致1 - 2个氨基酸替换。标记这些新等位基因的大多数核苷酸替换在其他HLA - B等位基因中也有发现,这表明基因转换和/或相互重组产生了这种多样性。所有氨基酸替换预计都会改变HLA - B分子的抗原结合位点。新定义的HLA - B等位基因产物最初是根据其异常的血清学反应模式来定义的。B8201等位基因产物在血清学上被分型为B“空白”或B22或B45的变体。这些模式以及其他新描述的等位基因产物的血清学反应与特定HLA - B分子之间的蛋白质序列同源性一致。虽然血清学仍然是检测HLA多样性的有力工具,但由导致基因座上等位基因间HLA序列多态性共享的事件产生的等位基因,将继续给分型结果的解读带来复杂性。