Rogde S, Mevåg B, Teisberg P, Gedde-Dahl T, Tedesco F, Olaisen B
Hum Genet. 1985;70(3):211-6. doi: 10.1007/BF00273444.
Extensive genetic polymorphism of complement component C8 was demonstrated by isoelectric focusing of serum or plasma samples followed by immunoblotting procedures. Using these methods, we could detect both alpha-gamma (C81) and beta (C82) chain polymorphisms in the same gel. Two-dimensional (2D) electrophoresis of C8 immunoprecipitates was used to obtain further information of the C8 patterns. Evidence was obtained that the C81 polymorphism resides in the structural gene of the C8 alpha chain. Both C8 systems show autosomal, chiefly codominant inheritance, and the distribution of phenotypes agrees with the Hardy-Weinberg equilibrium. Our findings suggest at least five different alleles in the C81 system; the gene frequencies of the two most common ones, C81A and C81B being 0.59 and 0.39, respectively. In C82 we found evidence for at least three codominant alleles, the gene frequencies for the two most common ones, C82B and C82A being 0.94 and 0.05, respectively. In addition, family studies disclosed the existence of a null allele, C82*Q0.
通过血清或血浆样本的等电聚焦,随后进行免疫印迹程序,证实了补体成分C8存在广泛的基因多态性。使用这些方法,我们能够在同一凝胶中检测到α-γ(C81)和β(C82)链多态性。对C8免疫沉淀物进行二维(2D)电泳,以获取有关C8模式的更多信息。有证据表明,C81多态性存在于C8α链的结构基因中。两个C8系统均显示常染色体遗传,主要为共显性遗传,且表型分布符合哈迪-温伯格平衡。我们的研究结果表明,C81系统中至少存在五个不同的等位基因;两个最常见的等位基因C81A和C81B的基因频率分别为0.59和0.39。在C82中,我们发现至少有三个共显性等位基因的证据,两个最常见的等位基因C82B和C82A的基因频率分别为0.94和0.05。此外,家系研究揭示了一个无效等位基因C82*Q0的存在。