Seegmiller R, Fraser F C, Sheldon H
J Cell Biol. 1971 Mar;48(3):580-93. doi: 10.1083/jcb.48.3.580.
The occurrence of a new mutation affecting cartilage and bone in mice is reported. The gene is lethal, shows autosomal recessive inheritance, and has high penetrance. It is not allelic to shorthead and probably not to phocomelia or achondroplasia. It results in a foreshortened face, cleft palate, defective trachea, and shortened long bones with flared metaphyses. Chondrocytes of epiphyseal cartilage from the mutant are not aligned in columns, and there is a decrease in the usual staining of the cartilage matrix. Electron microscope observations show large, wide collagen fibrils with "native" banding in the matrix of mutant cartilage, which are not present in normal cartilage. Possible explanations for the expression of this genetic disorder of cartilage development are put forward.
据报道,在小鼠中出现了一种影响软骨和骨骼的新突变。该基因是致死性的,表现为常染色体隐性遗传,且具有高外显率。它与短头基因非等位,可能也与短肢畸形或软骨发育不全基因非等位。它会导致面部缩短、腭裂、气管缺陷以及长骨缩短且干骺端增宽。突变体骨骺软骨的软骨细胞不成列排列,软骨基质的正常染色减少。电子显微镜观察显示,突变体软骨基质中有大而宽的具有“天然”条纹的胶原纤维,而正常软骨中不存在这种纤维。文中提出了关于这种软骨发育遗传疾病表达的可能解释。