Peptide binding function and the paradox of HLA disease associations

被引:32
作者
Hughes, AL
Yeager, M
Carrington, M
机构
[1] PENN STATE UNIV, INST MOL EVOLUT GENET, UNIVERSITY PK, PA 16802 USA
[2] NCI, BIOL CARCINOGENESIS & DEV PROGRAM, SAIC FREDERICK, FREDERICK CANC RES & DEV CTR, FREDERICK, MD 21701 USA
关键词
HLA/disease associations; major histocompatibility complex; peptide binding; recombination;
D O I
10.1038/icb.1996.74
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Many studies have found associations between HLA loci and susceptibility or resistance to both infectious and autoimmune diseases, but often subsequent studies fail to find the same association. Such inconsistencies are-not surprising if we consider what is known of the population biology and evolution of HLA genes, especially the consequences of natural selection favouring heterozygosity in the peptide binding regions (PER) of HLA molecules. Because of past recombination events and/or convergent evolution, alleles that are not closely related in overall sequence map come to resemble each other in the PBR. Because peptide binding is likely to be important for the role of HLA molecules in both infectious and autoimmune disease, a strategy of searching for HLA disease associations that groups alleles in functional categories based on PER motifs may prove more successful than conventional strategics, Likewise, in developing approaches for molecular typing, it may be advisable to develop methods that group alleles on the basis of shared PER motifs rather than simply on the basis of shared primer sites in less functionally important regions.
引用
收藏
页码:444 / 448
页数:5
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