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两个HLA - DR超型组基因的结构比较:编码DRw52和DRw53的基因座并非真正的等位基因。

Structural comparison of the genes of two HLA-DR supertypic groups: the loci encoding DRw52 and DRw53 are not truly allelic.

作者信息

Gorski J, Rollini P, Mach B

出版信息

Immunogenetics. 1987;25(6):397-402. doi: 10.1007/BF00396106.

Abstract

The organization and sequence of the HLA-DR beta chain genes are compared in the two supertypic groups, DRw52 and DRw53, which together account for more than 80% of HLA-DR alleles. From the structural data, we conclude that these two groups represent distinct lineages which have followed different patterns of evolution. The fine structure of the beta chain locus encoding the DRw53 specificity corresponds most closely to the DR beta II pseudogene in the DRw52 haplotypes. Concomitantly, the DR beta I locus in DRw53 haplotypes is more closely related to both of the two expressed DR beta loci of the DRw52 haplotypes (DR beta I and DR beta III). These two loci are the result of a recent duplication. This leads to the proposal that both expressed DR beta chain genes in the DRw52 haplotypes (DR beta I and DR beta III) are derived from a single precursor locus, while the two loci expressed in the DRw53 haplotypes are derived from distinct ancestral loci. The genes encoding DRw52 and DRw53 are therefore not true alleles of the same original locus. A scheme is proposed that accounts for the evolution of DR specificities within the DRw52 and DRw53 groups of haplotypes. It is evident that the different HLA-DR alleles are not structurally equidistant and that one must take into consideration different degrees of heterozygosity or mismatch among the DR alleles.

摘要

对HLA - DRβ链基因的组织和序列在两个超型组DRw52和DRw53中进行了比较,这两个超型组合计占HLA - DR等位基因的80%以上。根据结构数据,我们得出结论,这两个组代表了遵循不同进化模式的不同谱系。编码DRw53特异性的β链基因座的精细结构与DRw52单倍型中的DRβII假基因最为接近。同时,DRw53单倍型中的DRβI基因座与DRw52单倍型的两个表达的DRβ基因座(DRβI和DRβIII)的关系更为密切。这两个基因座是最近一次复制的结果。这导致了这样一种提议,即DRw52单倍型中的两个表达的DRβ链基因(DRβI和DRβIII)都源自单个前体基因座,而DRw53单倍型中表达的两个基因座则源自不同的祖先基因座。因此,编码DRw52和DRw53的基因不是同一原始基因座的真正等位基因。提出了一个方案来解释DRw52和DRw53单倍型组内DR特异性的进化。很明显,不同的HLA - DR等位基因在结构上并非等距,而且必须考虑DR等位基因之间不同程度的杂合性或错配。

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