Berg K, Powell L M, Wallis S C, Pease R, Knott T J, Scott J
Proc Natl Acad Sci U S A. 1986 Oct;83(19):7367-70. doi: 10.1073/pnas.83.19.7367.
The antigenic group (Ag) system of homospecific human serum antigens of low density lipoprotein is detected by antiserum from multiply transfused patients. A complex series of common Ag alleles has been described, but the biochemical nature of this polymorphism is uncertain. Here we report that DNA polymorphisms at the human apolipoprotein B (apoB) locus are very closely linked to alleles of the Ag system. We also show a strong association between Ag(x) and a polymorphism detected with the restriction endonuclease Xba I. We conclude that the immunologically determined Ag system represents protein polymorphism of apoB rather than primary genetic differences in posttranslational processing or lipid binding. These studies therefore demonstrate that the Ag locus is located on the short arm of human chromosome 2 in the region p23-p24 to which the apoB gene has been assigned. Since the Ag(x) antigen is associated with altered plasma lipid levels, this determinant may indicate a functionally important domain of apoB.
通过多次输血患者的抗血清检测低密度脂蛋白同种特异性人血清抗原的抗原组(Ag)系统。已描述了一系列复杂的常见Ag等位基因,但这种多态性的生化性质尚不确定。在此我们报告,人类载脂蛋白B(apoB)基因座处的DNA多态性与Ag系统的等位基因紧密连锁。我们还显示Ag(x)与用限制性内切酶Xba I检测到的一种多态性之间存在强关联。我们得出结论,免疫测定的Ag系统代表apoB的蛋白质多态性,而非翻译后加工或脂质结合方面的原发性遗传差异。因此,这些研究表明Ag基因座位于人类2号染色体短臂上apoB基因所定位的p23 - p24区域。由于Ag(x)抗原与血浆脂质水平改变有关,该决定簇可能指示apoB的一个功能重要结构域。