Margulies D H, Evans G A, Ozato K, Camerini-Otero R D, Tanaka K, Appella E, Seidman J G
J Immunol. 1983 Jan;130(1):463-70.
Among the more than 20 H-2-like genes in the BALB/c mouse genome, there are two classical transplantation antigens (H-2Dd and H-2Ld) encoded at the D-end of the major histocompatibility complex. Here we report the identification of a bacteriophage clone that encodes H-2Dd. The H-2Dd gene was identified by nucleotide sequence analysis and by characterization of the new H-2 antigen expressed when the cloned gene was introduced into mouse L cells by DNA-mediated gene transfer. The previously identified H-2Ld gene was then compared with the H-2Dd gene. The two genes appear to have the same general structure, and for the 854 nucleotides that have been compared, the two genes are 89% homologous. The H-2Ld and H-2Dd antigens expressed on mouse L cells after DNA-mediated gene transfer were examined by immunologic criteria. The stably transformed cell lines express apparently normal levels of H-2Dd and H-2Ld on the cell surface as measured by quantitative immunofluorescence by using monoclonal anti-H-2 antibodies. They synthesize H-2Dd and H-2Ld at normal rates as determined by endogenous labeling and immunoprecipitation of cell extracts. They evoke a strong specific serologic response when used to immunize C3H mice. The newly expressed antigens are able to serve as targets for alloreactive T cells. These cloned genes provide good substrates for examining the evolution of two closely linked H-2 antigen genes. Comparison of the structures of these genes provides clues to the basis for the differential expression of these antigens and their different biologic functions.
在BALB/c小鼠基因组中20多个类H-2基因中,有两个经典移植抗原(H-2Dd和H-2Ld)在主要组织相容性复合体的D端编码。在此我们报告了一个编码H-2Dd的噬菌体克隆的鉴定。通过核苷酸序列分析以及将克隆基因通过DNA介导的基因转移导入小鼠L细胞时所表达的新H-2抗原的特性鉴定出了H-2Dd基因。然后将先前鉴定出的H-2Ld基因与H-2Dd基因进行比较。这两个基因似乎具有相同的总体结构,在已比较的854个核苷酸中,这两个基因的同源性为89%。通过免疫学标准检查了DNA介导的基因转移后在小鼠L细胞上表达的H-2Ld和H-2Dd抗原。通过使用单克隆抗H-2抗体进行定量免疫荧光测定,稳定转化的细胞系在细胞表面表达的H-2Dd和H-2Ld水平明显正常。通过细胞提取物的内源性标记和免疫沉淀确定,它们以正常速率合成H-2Dd和H-2Ld。当用于免疫C3H小鼠时,它们会引发强烈的特异性血清学反应。新表达的抗原能够作为同种反应性T细胞的靶标。这些克隆基因是用于研究两个紧密连锁的H-2抗原基因进化的良好底物。对这些基因结构的比较为这些抗原差异表达及其不同生物学功能的基础提供了线索。