Yueh Y G, Gardner D P, Kappen C
Department of Biochemistry and Molecular Biology, Samuel C. Johnson Medical Research Center, Mayo Clinic Scottsdale, 13400 East Shea Boulevard, Scottsdale, AZ 85259, USA.
Proc Natl Acad Sci U S A. 1998 Aug 18;95(17):9956-61. doi: 10.1073/pnas.95.17.9956.
Homeobox genes of the Hox class are required for proper patterning of skeletal elements, but how they regulate the differentiation of specific tissues is unclear. We show here that overexpression of a Hoxc-8 transgene causes cartilage defects whose severity depends on transgene dosage. The abnormal cartilage is characterized by an accumulation of proliferating chondrocytes and reduced maturation. Since Hoxc-8 is normally expressed in chondrocytes, these results suggest that Hoxc-8 continues to regulate skeletal development well beyond pattern formation in a tissue-specific manner, presumably by controlling the progression of cells along the chondrocyte differentiation pathway. The comparison to Hoxd-4 and Isl-1 indicates that this role in chondrogenesis is specific to proteins of the Hox class. Their capacity for regulation of cartilage differentiation suggests that Hox genes could also be involved in human chondrodysplasias or other cartilage disorders.
Hox 类同源框基因对于骨骼元素的正确模式形成是必需的,但它们如何调节特定组织的分化尚不清楚。我们在此表明,Hoxc-8 转基因的过表达会导致软骨缺陷,其严重程度取决于转基因剂量。异常软骨的特征是增殖软骨细胞的积累和成熟减少。由于 Hoxc-8 通常在软骨细胞中表达,这些结果表明,Hoxc-8 以组织特异性方式在模式形成之后很长时间内持续调节骨骼发育,大概是通过控制细胞沿着软骨细胞分化途径的进程。与 Hoxd-4 和 Isl-1 的比较表明,这种在软骨形成中的作用是 Hox 类蛋白质所特有的。它们调节软骨分化的能力表明,Hox 基因也可能参与人类软骨发育不全或其他软骨疾病。