Hauptfeld V, Klein J
J Exp Med. 1975 Aug 1;142(2):288-98. doi: 10.1084/jem.142.2.288.
Molecular relationship of public H-2 antigens 1, 5, 6, 8, 11, 13, 25, and 28 to private antigens controlled by K and D regions was studied using the technique of antibody-induced resistance to complement-mediated cytotoxicity. The results indicate physical association in the cell membrane between H-2 antigens 1 and 23 of H-2-a, 8 and 31 of H-2-d, 11 and 17 of H-2-q, 13 and 30 of H-2-q, 25 and 23 of H-2-k, and 28 and 31 of H-2-g. These results are in agreement with genetic mapping placing the determinants of antigens H-2.8, 11 and 25 in the K region , the determinant of antigen H-2.13 in the D region, and the determinants of antigens H-2.1 and 28 in either the K or the D region. In contrast to genetic mapping placing the determinant for antigen H-2.6 in the D region, we found that in the H-2-b haplotype the antigen is associated with K region antigen H-2.33 and H-2.32, and interpreted this result as evidence for two homologous H-2.5 sites controlled by opposite ends of the H-2 complex. Although the data do not prove that public antigens are carried by the same molecules as private ones, they demonstrate a close physical association in the membrane between the two groups of loci, K and D, coding for the first 33 classical H-2 antigens (with the exception of antigen H-2.7), and thus support the two-locus model. The data also support the duplication model of H-2 by demonstrating two homologous H-2.5 sites associated with K and D molecules.
利用抗体诱导的对补体介导的细胞毒性的抗性技术,研究了公共H-2抗原1、5、6、8、11、13、25和28与由K和D区域控制的私有抗原之间的分子关系。结果表明,H-2-a的H-2抗原1和23、H-2-d的H-2抗原8和31、H-2-q的H-2抗原11和17、H-2-q的H-2抗原13和30、H-2-k的H-2抗原25和23以及H-2-g的H-2抗原28和31在细胞膜上存在物理关联。这些结果与基因定位一致,基因定位将抗原H-2.8、11和25的决定簇置于K区域,抗原H-2.13的决定簇置于D区域,抗原H-2.1和28的决定簇置于K或D区域。与将抗原H-2.6的决定簇定位在D区域的基因定位相反,我们发现,在H-2-b单倍型中,该抗原与K区域抗原H-2.33和H-2.32相关联,并将此结果解释为存在由H-2复合体相对末端控制的两个同源H-2.5位点的证据。尽管数据并未证明公共抗原与私有抗原由相同分子携带,但它们表明编码前33种经典H-2抗原(抗原H-2.7除外)的K和D两组基因座在膜上存在紧密的物理关联,从而支持双基因座模型。数据还通过证明与K和D分子相关的两个同源H-2.5位点,支持了H-2的重复模型。