Stratakis C A, Orban Z, Burns A L, Vottero A, Mitsiades C S, Marx S J, Abbassi V, Chrousos G P
Section on Pediatric Endocrinology, National Institute of Child Health and Human Development (NICHD), Bethesda, Maryland, 20892, USA.
Biochem Mol Med. 1996 Dec;59(2):112-7. doi: 10.1006/bmme.1996.0075.
Schmid metaphyseal chondrodysplasia (SMCD; MIM 156500) is an autosomal dominant disorder of the skeleton that is manifested in early childhood by short stature, coxa vara, and a waddling gait. Patients with SMCD have mutations in the gene that codes for the alpha-1 chain of collagen X (COL10A1); however, mutation analysis of this gene is hampered by its size. We studied a family with SMCD: the mother, a 36-year-old woman with a height of 149 cm, had mild bilateral coxa vara. Her two sons presented with short stature, bowed legs, and coxa vara in early childhood. DNA was extracted from peripheral lymphocytes from the three patients and subjected to PCR amplification by COL10A1 gene-specific primers. In addition to single-strand conformational polymorphism (SSCP) analysis of the COL10A1 gene, we used a novel method, dideoxy fingerprinting (ddF). The genetic defect in this family was found to be a previously unreported missense mutation (T-to-C transition) at nucleotide 2011. This change resulted in a Ser-to-Pro substitution at position 671 of the carboxy-terminus of the COL10A1 protein. In addition, the two boys, but not the mother, were found to carry a trinucleotide (CCC) deletion at position 2048 of the 3' untranslated region, a polymorphism of the COL10A1 gene. We conclude that ddF can be used in the analysis of the COL10A1 gene along with SSCP. The S671P substitution is novel, but located in the same region with the other reported COL10A1 mutations, confirming type X collagen as the locus for this disease.
施密德干骺端软骨发育不良(SMCD;MIM 156500)是一种常染色体显性遗传的骨骼疾病,在儿童早期表现为身材矮小、髋内翻和蹒跚步态。SMCD患者的编码胶原蛋白X(COL10A1)α-1链的基因发生突变;然而,该基因的突变分析因基因大小而受到阻碍。我们研究了一个患有SMCD的家族:母亲是一名36岁的女性,身高149厘米,有轻度双侧髋内翻。她的两个儿子在儿童早期出现身材矮小、弓形腿和髋内翻。从这三名患者的外周淋巴细胞中提取DNA,并使用COL10A1基因特异性引物进行PCR扩增。除了对COL10A1基因进行单链构象多态性(SSCP)分析外,我们还使用了一种新方法——双脱氧指纹图谱(ddF)。发现该家族的遗传缺陷是核苷酸2011处一个以前未报道的错义突变(T到C转换)。这种变化导致COL10A1蛋白羧基末端第671位的丝氨酸被脯氨酸取代。此外,发现两个男孩而非母亲在3'非翻译区的2048位携带一个三核苷酸(CCC)缺失,这是COL10A1基因的一种多态性。我们得出结论,ddF可与SSCP一起用于COL10A1基因的分析。S671P取代是新发现的,但位于与其他已报道的COL10A1突变相同的区域,证实X型胶原蛋白是该疾病的致病位点。