Diab M, Wu J J, Shapiro F, Eyre D
Department of Orthopedics, University of Washington, Seattle 98195.
Am J Med Genet. 1994 Feb 15;49(4):402-9. doi: 10.1002/ajmg.1320490411.
There is growing evidence that a spectrum of chondrodysplasias are caused by mutations in the gene coding for type II collagen. The basic molecular defect in diastrophic dysplasia has not been defined, but it appears not to be in collagen type II. Cartilage contains other tissue-specific collagens, types IX, X, and XI, but no mutations have yet been found in their genes in clinical disease. Type IX collagen is hypothesized to play a role in the regulation of type II collagen fibril organization and structure in cartilage extracellular matrix. In this study, we have examined iliac crest growth cartilage from a patient with diastrophic dysplasia. Although collagen fibrils were markedly increased in diameter on transmission electron microscopy, type II collagen appeared to be normal biochemically. Type XI collagen was also normal. However, type IX collagen appeared abnormal on sodium dodecyl sulfate polyacrylamide gel electrophoresis with a pronounced excess of the COL1 domain of the molecule in pepsin extracts. The findings point to an abnormality in structure or metabolism of type IX collagen in diastrophic dysplasia.
越来越多的证据表明,一系列软骨发育不良是由编码II型胶原蛋白的基因突变引起的。扭曲性发育不良的基本分子缺陷尚未明确,但似乎不在II型胶原蛋白中。软骨含有其他组织特异性胶原蛋白,即IX型、X型和XI型,但在临床疾病中尚未发现它们的基因发生突变。据推测,IX型胶原蛋白在软骨细胞外基质中II型胶原纤维的组织和结构调节中起作用。在本研究中,我们检查了一名扭曲性发育不良患者的髂嵴生长软骨。尽管在透射电子显微镜下胶原纤维直径明显增加,但II型胶原蛋白在生化方面似乎是正常的。XI型胶原蛋白也是正常的。然而,在十二烷基硫酸钠聚丙烯酰胺凝胶电泳上,IX型胶原蛋白出现异常,胃蛋白酶提取物中该分子的COL1结构域明显过量。这些发现表明扭曲性发育不良中IX型胶原蛋白的结构或代谢存在异常。