Rogde S, Teisberg P, Olaisen B
Institute of Forensic Medicine, University of Oslo, Norway.
Hum Hered. 1989;39(2):81-8. doi: 10.1159/000153839.
C8 inheritance patterns in 364 mother-child pairs formed the basis for evaluation of the existence of silent alleles (null alleles) in the genes determining the two known polymorphic C8 systems. While evidence for such alleles was not found in C8A (alpha-gamma complex), two observations of null allele segregation in C8B (beta chain) indicate a C8BQ0 allele frequency of about 0.07. Two population samples comprising 150 Lappish and 1,264 non-Lappish Norwegians were examined for phenotype distributions in C8A and C8B. The phenotype distributions were mainly in accordance with the expected Hardy-Weinberg distribution. The results for C8A indicated simple, codominant inheritance of two frequent and several rare alleles. Allele frequencies were similar in the two populations. The C8A B gene frequency in Norwegians was significantly lower than that in FRG and higher than that in Negroes. C8B allele frequencies were also calculated from gene counts in the population material, but with due corrections for the C8BQ0 frequency observed in the mother-child material.
364对母婴的C8遗传模式构成了评估决定两种已知多态性C8系统的基因中沉默等位基因(无效等位基因)是否存在的基础。虽然在C8A(α-γ复合物)中未发现此类等位基因的证据,但在C8B(β链)中有两例无效等位基因分离的观察结果表明C8BQ0等位基因频率约为0.07。对由150名拉普人及1264名非拉普挪威人组成的两个群体样本进行了C8A和C8B表型分布的检测。表型分布主要符合预期的哈迪-温伯格分布。C8A的结果表明两个常见和几个罕见等位基因呈简单共显性遗传。两个群体中的等位基因频率相似。挪威人中C8A B基因频率显著低于德国,高于黑人。C8B等位基因频率也根据群体材料中的基因计数计算得出,但对母婴材料中观察到的C8BQ0频率进行了适当校正。