Jenner K, Sidoli A, Ball M, Rodriguez J R, Pagani F, Giudici G, Vergani C, Mann J, Baralle F E, Shoulders C C
Sir William Dunn School of Pathology, University of Oxford, U.K.
Atherosclerosis. 1988 Jan;69(1):39-49. doi: 10.1016/0021-9150(88)90287-0.
The 3' end of the apo B gene is highly polymorphic. Two point mutations in the coding sequence of the gene create EcoRI (E+, E-) and XbaI (X+, X-) RFLPs. The two loci are in random association and the frequency of the four haplotypes, E+X+, E+X-, E-X+ and E-X- in the normolipidaemic population are 0.68, 0.30, 0.02 and 0.00, respectively. Although the polymorphic nucleotide underlying the EcoRI RFLP creates an amino acid substitution in the apo B protein (Glu----Lys) in a region close to a putative LDL-receptor recognition site(s), we find no statistically significant difference in the frequency of the apo BGlu and apo BLys alleles in hyperlipidaemic patients (familial hypercholesterolaemia, type IIA with no tendon xanthomas, IIB and probably IV) and the normolipidaemic population. In contrast, we confirm previous findings, that the X+ allele is in linkage disequilibrium with a genetic locus that predisposes to the development of higher fasting plasma triglyceride levels than the X- allele. We have characterized a highly polymorphic region immediately 3' to the apo B gene. At least 5 alleles of this locus exist in the population and our family studies show it should be an extremely informative locus to use in studies where polymorphic or mutant apo B alleles are suspected to underly certain forms of familial hyperlipidaemia. DNA sequence analysis of this highly polymorphic locus shows that the variation is entirely attributable to the number of times the simple repeating sequence 5'-TTTATAATTAAAATATTTATAATTAAATAT-3' is present.
载脂蛋白B基因的3'端具有高度多态性。该基因编码序列中的两个点突变产生了EcoRI(E +,E -)和XbaI(X +,X -)限制性片段长度多态性。这两个位点呈随机关联,在血脂正常人群中四种单倍型E + X +、E + X -、E - X +和E - X -的频率分别为0.68、0.30、0.02和0.00。尽管EcoRI限制性片段长度多态性所对应的多态核苷酸在靠近假定的低密度脂蛋白受体识别位点的区域内导致了载脂蛋白B蛋白中的氨基酸替换(Glu→Lys),但我们发现在高脂血症患者(家族性高胆固醇血症,IIA型无腱黄瘤、IIB型以及可能的IV型)和血脂正常人群中,载脂蛋白BGlu和载脂蛋白BLys等位基因的频率没有统计学上的显著差异。相反,我们证实了先前的发现,即X +等位基因与一个基因位点存在连锁不平衡,该基因位点易导致空腹血浆甘油三酯水平高于X -等位基因。我们已经对载脂蛋白B基因3'端紧邻的一个高度多态性区域进行了特征分析。该位点在人群中至少存在5个等位基因,我们的家系研究表明,在怀疑多态或突变的载脂蛋白B等位基因是某些形式的家族性高脂血症基础的研究中,它应该是一个极具信息量的位点。对这个高度多态性位点的DNA序列分析表明,变异完全归因于简单重复序列5'-TTTATAATTAAAATATTTATAATTAAATAT-3'出现的次数。