Ferrell R E, Kamboh M I, Majumder P P, Valdez R, Weiss K M
Human Genetics Division, Graduate School of Public Health, University of Pittsburgh, Pa.
Hum Hered. 1990;40(3):127-35. doi: 10.1159/000153919.
Apolipoprotein C-III (APO C-III) is a structural component of very-low-density and high-density lipoprotein particles and is an inhibitor of lipoprotein lipase. In a study of genetic variation of apolipoproteins in the Mayan population of the Yucatán peninsula, we observed a quantitative polymorphism in APO C-III levels. This polymorphism is expressed as variation in immunoblot staining intensity following isoelectric focusing and as variation in plasma levels of APO C-III determined by radial immunodiffusion. This variation is consistent with the presence in Mayans of an allele associated with low levels of plasma APO C-III which we have designated APO C-III*D. Analysis of the distribution of APO C-III levels yields a gene frequency estimate for the deficiency allele of 0.59. There is a significant positive correlation between total plasma APO C-III levels and total plasma cholesterol and triglyceride levels, the lowest levels of cholesterol and triglycerides being seen in individuals homozygous for the deficiency allele. This observation is consistent with the proposed role of APO C-III in lipoprotein metabolism. Family data to determine whether this deficiency allele is due to mutation at the APO C-III structural locus were not available. However, molecular analysis using cloned probes from the APO A-I/C-III/A-IV gene cluster revealed no gross DNA rearrangement or deletion of sequences in this region in homozygous deficient individuals.
载脂蛋白C-III(APO C-III)是极低密度脂蛋白和高密度脂蛋白颗粒的结构成分,是脂蛋白脂肪酶的抑制剂。在对尤卡坦半岛玛雅人群载脂蛋白基因变异的研究中,我们观察到APO C-III水平存在数量多态性。这种多态性表现为等电聚焦后免疫印迹染色强度的变化,以及通过放射免疫扩散测定的血浆APO C-III水平的变化。这种变化与玛雅人中存在与低血浆APO C-III水平相关的等位基因一致,我们将其命名为APO C-III*D。对APO C-III水平分布的分析得出缺陷等位基因的基因频率估计值为0.59。血浆总APO C-III水平与血浆总胆固醇和甘油三酯水平之间存在显著正相关,在缺陷等位基因纯合个体中观察到胆固醇和甘油三酯水平最低。这一观察结果与APO C-III在脂蛋白代谢中所提出的作用一致。无法获得用于确定该缺陷等位基因是否由于APO C-III结构基因座突变的家系数据。然而,使用来自APO A-I/C-III/A-IV基因簇的克隆探针进行的分子分析显示,纯合缺陷个体在该区域没有明显的DNA重排或序列缺失。