Department of Orthopaedics, Kyoto University, 54 Kawahara-cho, Shogoin, Sakyo, Kyoto, Japan.
J Bone Miner Metab. 2011 Jan;29(1):123-9. doi: 10.1007/s00774-010-0206-z. Epub 2010 Jul 30.
Sox9 belongs to the family of Sry-related high-mobility group box transcription factors controlling cell fate, cell proliferation and differentiation in various tissues, including cartilage, testis, the central nervous system, kidney, and gastrointestine. Mice conditionally lacking Sox9 have revealed essential roles for Sox9 in these tissues. To gain further insight into the role of Sox9 in different tissues and at different stages of development, we have generated a transgenic mouse line to express Sox9 in a Cre recombinase-dependent manner. The construct contained the human cytomegalovirus enhancer and chicken β-actin promoter, and a floxed monomeric red fluorescence protein 1 (mRFP1) cassette to direct ubiquitous expression of mRFP1. Cre expression removed the mRFP1 gene, allowing expression of Sox9 and enhanced green fluorescent protein. Expectedly, overexpression of Sox9 in chondrocytes using Col2a1-Cre mice suppressed chondrocyte hypertrophy, and delayed terminal differentiation and subsequent ossification. Misexpression of Sox9 in hypertrophic chondrocytes using Col10a1-Cre knock-in mice also delayed terminal differentiation. This Sox9 conditional transgenic mouse line will be a valuable tool to uncover tissue-specific and developmental stage-specific functions of Sox9.
Sox9 属于 Sry 相关高迁移率族盒转录因子家族,可控制包括软骨、睾丸、中枢神经系统、肾脏和胃肠道在内的各种组织中的细胞命运、细胞增殖和分化。条件性缺乏 Sox9 的小鼠揭示了 Sox9 在这些组织中的重要作用。为了更深入地了解 Sox9 在不同组织和发育阶段的作用,我们构建了一种 Sox9 在 Cre 重组酶依赖性方式下表达的转基因小鼠系。该构建体包含人巨细胞病毒增强子和鸡 β-肌动蛋白启动子,以及一个 floxed 单体红色荧光蛋白 1(mRFP1)盒,以指导 mRFP1 的普遍表达。Cre 表达去除了 mRFP1 基因,允许 Sox9 和增强型绿色荧光蛋白的表达。使用 Col2a1-Cre 小鼠过表达软骨细胞中的 Sox9 可抑制软骨细胞肥大,并延迟终末分化和随后的骨化。在 Col10a1-Cre 基因敲入小鼠的肥大软骨细胞中异位表达 Sox9 也会延迟终末分化。这种 Sox9 条件性转基因小鼠系将成为揭示 Sox9 组织特异性和发育阶段特异性功能的有用工具。