Vikkula M, Ritvaniemi P, Vuorio A F, Kaitila I, Ala-Kokko L, Peltonen L
Department of Human Molecular Genetics, National Public Health Institute, Helsinki, Finland.
Genomics. 1993 Apr;16(1):282-5. doi: 10.1006/geno.1993.1179.
Type II collagen is coded by a large gene (COL2A1) consisting of 54 exons on chromosome 12. During the past few years several cartilage disorders have been linked to this gene, and some specific nucleotide changes have been identified in patients. In a spondyloepiphyseal form of chondrodysplasia, the three mutations found so far are all in exon 48 in the region coding for the carboxyl-terminal end of the triple helix. Since folding of the type II collagen polypeptides to the triple helix is initiated from the carboxyl-terminal end, it has been suggested that mutations in this region typically result in severe cartilage diseases. Here we report a novel mutation located in the area coding for the amino-terminal part of the triple helix in a sporadic patient with spondyloepiphyseal dysplasia (SED). The mutation, a substitution of G1063 to A, which results in the conversion of Gly154 to Arg, was identified using exon-specific amplification of genomic DNA and subsequent analyses with denaturing gradient gel electrophoresis and single-strand conformation polymorphism. The substitution was not found in any other SED patient in Finland. This novel mutation demonstrates that amino acid substitutions in the amino-terminal part of the type II collagen triple helix can also result in SED.
II型胶原蛋白由位于12号染色体上的一个由54个外显子组成的大基因(COL2A1)编码。在过去几年中,几种软骨疾病已与该基因相关联,并且在患者中已鉴定出一些特定的核苷酸变化。在一种脊椎骨骺型软骨发育不良中,迄今为止发现的三个突变都位于编码三螺旋羧基末端区域的第48外显子中。由于II型胶原蛋白多肽折叠成三螺旋是从羧基末端开始的,因此有人提出该区域的突变通常会导致严重的软骨疾病。在这里,我们报告了一名患有脊椎骨骺发育不良(SED)的散发性患者中,在编码三螺旋氨基末端部分的区域发现的一个新突变。该突变是G1063被A取代,导致Gly154转换为Arg,通过基因组DNA的外显子特异性扩增以及随后的变性梯度凝胶电泳和单链构象多态性分析得以鉴定。在芬兰的任何其他SED患者中均未发现该取代。这个新突变表明,II型胶原蛋白三螺旋氨基末端部分的氨基酸取代也可导致SED。