Department of Molecular and Cellular Biochemistry, Osaka University Graduate School of Dentistry, Osaka, Japan.
Department of Orthopedics, Nippon Medical School, Tokyo, Japan.
Commun Biol. 2021 Mar 11;4(1):326. doi: 10.1038/s42003-021-01848-1.
Endochondral bone formation is fundamental for skeletal development. During this process, chondrocytes undergo multiple steps of differentiation and coordinated transition from a proliferating to a hypertrophic stage, which is critical to advance skeletal development. Here, we identified the transcription factor Dmrt2 (double-sex and mab-3 related transcription factor 2) as a Sox9-inducible gene that promotes chondrocyte hypertrophy in pre-hypertrophic chondrocytes. Epigenetic analysis further demonstrated that Sox9 regulates Dmrt2 expression through an active enhancer located 18 kb upstream of the Dmrt2 gene and that this enhancer's chromatin status is progressively activated through chondrocyte differentiation. Dmrt2-knockout mice exhibited a dwarf phenotype with delayed initiation of chondrocyte hypertrophy. Dmrt2 augmented hypertrophic chondrocyte gene expression including Ihh through physical and functional interaction with Runx2. Furthermore, Dmrt2 deficiency reduced Runx2-dependent Ihh expression. Our findings suggest that Dmrt2 is critical for sequential chondrocyte differentiation during endochondral bone formation and coordinates the transcriptional network between Sox9 and Runx2.
软骨内骨形成对于骨骼发育至关重要。在这个过程中,软骨细胞经历了多个分化步骤,并协调地从增殖期过渡到肥大期,这对于推进骨骼发育至关重要。在这里,我们确定转录因子 Dmrt2(双性和 mab-3 相关转录因子 2)是 Sox9 诱导的基因,可促进预肥大软骨细胞中的软骨细胞肥大。表观遗传分析进一步表明,Sox9 通过位于 Dmrt2 基因上游 18kb 的活性增强子来调节 Dmrt2 的表达,并且该增强子的染色质状态通过软骨细胞分化逐渐被激活。Dmrt2 敲除小鼠表现出矮小表型,软骨细胞肥大的起始延迟。Dmrt2 通过与 Runx2 的物理和功能相互作用,增强了包括 Ihh 在内的肥大软骨细胞基因的表达。此外,Dmrt2 缺乏会降低依赖于 Runx2 的 Ihh 表达。我们的研究结果表明,Dmrt2 对于软骨内骨形成过程中的连续软骨细胞分化至关重要,并协调 Sox9 和 Runx2 之间的转录网络。