Hansen T H, Cullen S E, Melvold R, Kohn H, Flaherty L, Sachs D H
J Exp Med. 1977 Jun 1;145(6):1550-8. doi: 10.1084/jem.145.6.1550.
Sequential precipitations of soluble BALB/c antigen with antisera detecting private and public H-2 specificities indicated three distinct classes of molecules of 45,000 mol wt. However, only two of these classes of molecules were detectable in antigen from the loss mutant, BALB/c-H-2db. The class of molecules, detectable in the wild-type strain but missing in the mutant, does not bear private specificities but does react with an antiserum detecting H-2 public specificities. Absorption in mutant mice of the antiserum to public specificities, left antibodies specific for the antigen detectable in BALB/c but not BALB/c-H-2db. Genetic mapping studies using this specific antiserum indicated that the antigenic loss of this mutant is in a gene which maps in or close to the H-2D region, separable from the H-2K, S, G, Qa-2, and Tla regions.
用检测H-2私有和公有特异性的抗血清对可溶性BALB/c抗原进行连续沉淀,结果表明存在三种不同类型的分子量为45,000的分子。然而,在缺失突变体BALB/c-H-2db的抗原中只能检测到其中两类分子。在野生型菌株中可检测到但在突变体中缺失的那类分子,不带有私有特异性,但确实能与检测H-2公有特异性的抗血清发生反应。用抗公有特异性的抗血清在突变小鼠中进行吸收,留下了对BALB/c中可检测到但BALB/c-H-2db中不可检测到的抗原具有特异性的抗体。使用这种特异性抗血清进行的基因定位研究表明,该突变体的抗原缺失位于一个基因中,该基因定位于H-2D区域内或附近,与H-2K、S、G、Qa-2和Tla区域可分离。