Soria L F, Ludwig E H, Clarke H R, Vega G L, Grundy S M, McCarthy B J
Gladstone Foundation Laboratories for Cardiovascular Disease, University of California, San Francisco 94140-0608.
Proc Natl Acad Sci U S A. 1989 Jan;86(2):587-91. doi: 10.1073/pnas.86.2.587.
Familial defective apolipoprotein (apo) B-100 is a genetic disease that leads to hypercholesterolemia and to an increased serum concentration of low density lipoproteins that bind defectively to the apoB,E(LDL) receptor. The disorder appears to result from a mutation in the gene for apoB-100. Extensive sequence analysis of the two alleles of one subject heterozygous for the disorder has revealed a previously unreported mutation in the codon for amino acid 3500 that results in the substitution of glutamine for arginine. This same mutant allele occurs in six other, unrelated subjects and in eight affected relatives in two of these families. A partial haplotype of this mutant apoB-100 allele was constructed by sequence analysis and restriction enzyme digestion at positions where variations in the apoB-100 are known to occur. This haplotype is the same in three probands and four affected members of one family and lacks a polymorphic Xba I site whose presence has been correlated with high cholesterol levels. Thus, it appears that the mutation in the codon for amino acid 3500 (CGG----CAG), a CG mutational "hot spot," defines a minor apoB-100 allele associated with defective low density lipoproteins and hypercholesterolemia.
家族性载脂蛋白(apo)B - 100缺陷是一种导致高胆固醇血症的遗传性疾病,可使与apoB,E(LDL)受体结合缺陷的低密度脂蛋白血清浓度升高。该病症似乎是由apoB - 100基因的突变引起的。对一名患有该病症的杂合子受试者的两个等位基因进行广泛的序列分析,发现了一个此前未报道的位于第3500位氨基酸密码子的突变,该突变导致谷氨酰胺替代精氨酸。在其他六个不相关的受试者以及其中两个家族的八个患病亲属中也发现了相同的突变等位基因。通过对已知apoB - 100发生变异的位置进行序列分析和限制性内切酶消化,构建了该突变apoB - 100等位基因的部分单倍型。在一个家族的三名先证者和四名患病成员中,这种单倍型是相同的,并且缺少一个与高胆固醇水平相关的多态性Xba I位点。因此,第3500位氨基酸密码子(CGG----CAG)的突变,即一个CG突变“热点”,似乎定义了一个与缺陷性低密度脂蛋白和高胆固醇血症相关的次要apoB - 100等位基因。