Andersson G
Uppsala Genetic Center, Box 7080, Swedish University of Agricultural Sciences, S-750 07 Uppsala, Sweden.
Front Biosci. 1998 Jul 27;3:d739-45. doi: 10.2741/a317.
The genomic organization and number of human HLA-DRB class II genes differs between haplotypes in the human population. In contrast, both HLA-DQ and -DP class II subregions are conserved. Understanding of the evolutionary relationship and age of HLA-DR haplotypes has been obtained by nucleotide sequence determination and phylogenetic analyses of intron sequences of all known DRB genes from different DR haplotypes. These analyses have indicated that the gene organization of some haplotypes has remained conserved for tens of millions of years and that novel haplotypes have originated during hominoid speciation. Thus, in the contemporary human population, both ancestral and species-specific DRB gene organizations are found. The plasticity of DR gene organization as well as the extensive allelic polymorphism of expressed DR-beta molecules are features which suggest that DR molecules are under distinct selective pressure compared to HLA-DQ and HLA-DP class II molecules. The extensive allelic polymorphism of HLA-DR transplantation antigens is exclusively provided by the beta-chain of these heterodimeric antigen presenting molecules. Most of this polymorphism appears to have been generated recently. Thus, evolutionary mechanisms involved in the preservation of ancestral gene organizations, selection against DR-alpha polymorphism, creation of DR-beta allelic polymorphism and generation of novel gene organizations are acting on the HLA-DR region simultaneously.
人类群体中不同单倍型的人类HLA - DRB II类基因的基因组组织和数量存在差异。相比之下,HLA - DQ和 - DP II类亚区域是保守的。通过对来自不同DR单倍型的所有已知DRB基因的内含子序列进行核苷酸序列测定和系统发育分析,已了解到HLA - DR单倍型的进化关系和年代。这些分析表明,某些单倍型的基因组织已经保持保守数千万年,并且新的单倍型在类人猿物种形成过程中产生。因此,在当代人类群体中,既发现了祖先的DRB基因组织,也发现了物种特异性的DRB基因组织。DR基因组织的可塑性以及表达的DR - β分子广泛的等位基因多态性表明,与HLA - DQ和HLA - DP II类分子相比,DR分子受到不同的选择压力。HLA - DR移植抗原广泛的等位基因多态性完全由这些异二聚体抗原呈递分子的β链提供。这种多态性大多似乎是最近产生的。因此,涉及保存祖先基因组织、针对DR - α多态性的选择、DR - β等位基因多态性的产生以及新基因组织的产生的进化机制同时作用于HLA - DR区域。