Miric A, Levine M A
Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
J Clin Endocrinol Metab. 1992 Mar;74(3):509-16. doi: 10.1210/jcem.74.3.1740484.
Familial isolated hypoparathyroidism (FIH) is an inherited metabolic disorder characterized by hypocalcemia and hyperphosphatemia due to deficient secretion of biologically active PTH. We used denaturing gradient gel electrophoresis to screen for mutations in exon 1 and the coding region of the preproPTH gene. Exons 1, 2, and 3 of the preproPTH gene and flanking intronic regions were amplified by polymerase chain reaction using primers that were designed employing the MELT-MAP program. One oligonucleotide from each primer pair was synthesized with a 5'-GC-clamp. Screening of amplified DNA from normal subjects and patients with FIH revealed two single base changes that altered migration of amplified preproPTH gene fragments through denaturing gels: 1) an A----G transition in intron 1; 10 nucleotides upstream of exon 2; and 2) a C----A transversion in exon 3 that conserves the arginine residue at codon 52 (CGA----AGA). By contrast, we did not detect pathogenic mutations in amplified regions of the preproPTH genes of 18 affected members of 5 FIH kindreds. The two polymorphisms occur frequently, and were therefore used to perform linkage analysis in 5 multiplex FIH families. Linkage analysis was inconclusive in 2 families and showed discordance between hypoparathyroidism and any of the preproPTH gene alleles in 2 other families. In another family, analysis was suggestive of linkage between hypoparathyroidism and inheritance of a specific preproPTH gene allele. These results indicate that denaturing gradient gel electrophoresis can be used to identify mutations in defined regions of the preproPTH gene, and to examine linkage of specific preproPTH alleles and inherited disorders of mineral metabolism.
家族性孤立性甲状旁腺功能减退症(FIH)是一种遗传性代谢紊乱疾病,其特征为生物活性甲状旁腺激素(PTH)分泌不足导致低钙血症和高磷血症。我们使用变性梯度凝胶电泳来筛查前甲状旁腺素原(preproPTH)基因第1外显子和编码区的突变。使用通过MELT-MAP程序设计的引物,通过聚合酶链反应扩增preproPTH基因的第1、2和3外显子以及侧翼内含子区域。每个引物对中的一个寡核苷酸合成时带有5'-GC夹。对正常受试者和FIH患者的扩增DNA进行筛查,发现了两个单碱基变化,这些变化改变了扩增的preproPTH基因片段在变性凝胶中的迁移:1)内含子1中,外显子2上游10个核苷酸处发生A→G转换;2)外显子3中发生C→A颠换,该颠换使密码子52处的精氨酸残基保持不变(CGA→AGA)。相比之下,我们在5个FIH家系的18名患病成员的preproPTH基因扩增区域中未检测到致病突变。这两个多态性频繁出现,因此用于对5个多重FIH家系进行连锁分析。2个家系的连锁分析结果不明确,另外2个家系中甲状旁腺功能减退症与任何preproPTH基因等位基因之间存在不一致。在另一个家系中,分析提示甲状旁腺功能减退症与特定preproPTH基因等位基因的遗传之间存在连锁关系。这些结果表明,变性梯度凝胶电泳可用于鉴定preproPTH基因特定区域的突变,并检测特定preproPTH等位基因与遗传性矿物质代谢紊乱之间的连锁关系。