Paolucci E S, Shreffler D C
Immunogenetics. 1983;17(1):67-78. doi: 10.1007/BF00364290.
A hemolytic assay has been developed which is specific for Factor B (B) activity in murine EDTA-plasma. Three discrete levels of B activity were observed among B10-congenic strains. Mice with standard H-2 haplotypes, b, d, k, r, f, q, s, and u, all exhibited the same mean level of activity. However, plasma from H-2v (B10.SM) mice contained only 0.25 of that level, and those with standard haplotype H-2ja (B10.WB) or wild haplotype H-2wr7 (B10.WR) exhibited 2.5 times the H-2b (B10) basal level of activity. These differences among B10 congenic lines suggested that the activity is H-2 controlled; further tentative mapping with intra-H-2 recombinants indicated that the gene is located in the S region. A fourth phenotype was found among progeny of backcross generations between B10.BR (H-2k) and mice of subspecies Mus musculus molossinus and M. m. bactrianus. This ultra-high activity was found also to be governed by a gene very closely linked to Ss, the primary S region marker. F1 generations between disparate phenotypes yielded progeny with activity levels intermediate between the parents; progeny of parents of different strains with the same phenotype expressed B hemolytic titres equal to those of the parental strains. No differences in antigenic levels of the protein among the strains of different phenotypes could be detected by radial immunodiffusion. In mixing experiments, resultant activity levels were intermediate between the higher and the lower phenotype, ruling out independent inhibitors or activators of the reaction. These studies indicate that an H-2-linked S region-located single gene governs structural differences in allelic B molecules that lead to differences in specific activities.
已开发出一种溶血测定法,该方法对鼠EDTA血浆中的B因子(B)活性具有特异性。在B10同源基因品系中观察到三种不同水平的B活性。具有标准H-2单倍型b、d、k、r、f、q、s和u的小鼠均表现出相同的平均活性水平。然而,H-2v(B10.SM)小鼠的血浆中该活性水平仅为上述水平的0.25,而具有标准单倍型H-2ja(B10.WB)或野生单倍型H-2wr7(B10.WR)的小鼠表现出的活性是H-2b(B10)基础活性水平的2.5倍。B10同源系之间的这些差异表明该活性受H-2控制;用H-内重组体进行的进一步初步定位表明该基因位于S区域。在B10.BR(H-2k)与小家鼠亚种小家鼠和中亚小家鼠的回交后代中发现了第四种表型。这种超高活性也由一个与主要S区域标记Ss紧密连锁的基因控制。不同表型之间的F1代产生的后代活性水平介于亲本之间;具有相同表型的不同品系亲本的后代表达的B溶血滴度与亲本品系相同。通过放射免疫扩散无法检测到不同表型品系之间蛋白质抗原水平的差异。在混合实验中,所得活性水平介于较高和较低表型之间,排除了反应的独立抑制剂或激活剂。这些研究表明,一个与H-2连锁的位于S区域的单基因控制等位基因B分子的结构差异,从而导致比活性的差异。