Del Pozzo G, Guardiola J
International Institute of Genetics and Biophysics, CNR, Napoli, Italy.
Immunogenetics. 1990;31(4):229-32. doi: 10.1007/BF00204892.
The class II region of the human major histocompatibility complex (MHC) contains a cluster of highly polymorphic genes organized into at least three subloci (DR, DQ, and DP), each encoding a subset of surface antigens participating in the modulation of the immune response. Genetic diversity in this system is brought about by two major mechanisms, hypermutation and trans-species evolution. The DQ subregion contains a pair of closely related A genes, HLA-DQA1 and HLA-DQA2, whose phylogenetic relationship is uncertain, although their generation by duplication of an ancestral A gene before or after speciation can be implied. We report here the presence of a member of the Alu repetitive family immediately 5' to the HLA-DQA1 gene. The sequence of this element indicates that it may have integrated by transposition at the time of divergence of hominoids from Old World monkeys. HLA-DQA2 carries an empty integration target site in place of the Alu, thereby suggesting that the insertion of Alu near HLA-DQA1 was preceded by the separation of the two genes.
人类主要组织相容性复合体(MHC)的II类区域包含一组高度多态的基因,这些基因至少被组织成三个亚位点(DR、DQ和DP),每个亚位点编码参与免疫反应调节的表面抗原子集。该系统中的遗传多样性由两种主要机制引起,即高突变和跨物种进化。DQ亚区域包含一对密切相关的A基因,即HLA - DQA1和HLA - DQA2,尽管可以推测它们是在物种形成之前或之后通过祖先A基因的复制产生的,但其系统发育关系尚不确定。我们在此报告,在HLA - DQA1基因的5'端紧邻处存在一个Alu重复家族的成员。该元件的序列表明,它可能是在类人猿与旧世界猴分化时通过转座整合进去的。HLA - DQA2携带一个空的整合靶位点,而不是Alu,因此表明在HLA - DQA1附近插入Alu之前,这两个基因已经分离。