Department of Molecular and Cellular Biochemistry, Osaka University Graduate School of Dentistry, 1-8 Yamadaoka, Suita, Osaka, 565-0871, Japan.
Department of Orthodontics and Dentofacial Orthopedics, Osaka University Graduate School of Dentistry, 1-8 Yamadaoka, Suita, Osaka, 565-0871, Japan.
Commun Biol. 2021 Nov 3;4(1):1258. doi: 10.1038/s42003-021-02793-9.
Endochondral ossification is regulated by transcription factors that include SRY-box transcription factor 9, runt-related protein 2 (Runx2), and Osterix. However, the sequential and harmonious regulation of the multiple steps of endochondral ossification is unclear. This study identified zinc finger homeodomain 4 (Zfhx4) as a crucial transcriptional partner of Osterix. We found that Zfhx4 was highly expressed in cartilage and that Zfhx4 deficient mice had reduced expression of matrix metallopeptidase 13 and inhibited calcification of cartilage matrices. These phenotypes were very similar to impaired chondrogenesis in Osterix deficient mice. Coimmunoprecipitation and immunofluorescence indicated a physical interaction between Zfhx4 and Osterix. Notably, Zfhx4 and Osterix double mutant mice showed more severe phenotype than Zfhx4 deficient mice. Additionally, Zfhx4 interacted with Runx2 that functions upstream of Osterix. Our findings suggest that Zfhx4 coordinates the transcriptional network of Osterix and, consequently, endochondral ossification.
软骨内骨化受转录因子调控,包括性决定区 Y 框转录因子 9、 runt 相关转录因子 2(Runx2)和骨形成蛋白 2(Osterix)。然而,软骨内骨化的多个步骤的顺序和协调调节尚不清楚。本研究确定锌指同源框 4(Zfhx4)是 Osterix 的关键转录伙伴。我们发现 Zfhx4 在软骨中高表达,Zfhx4 缺失小鼠的基质金属蛋白酶 13 表达降低,软骨基质钙化受到抑制。这些表型与 Osterix 缺失小鼠的软骨形成障碍非常相似。共免疫沉淀和免疫荧光表明 Zfhx4 和 Osterix 之间存在物理相互作用。值得注意的是,Zfhx4 和 Osterix 双突变小鼠的表型比 Zfhx4 缺失小鼠更为严重。此外,Zfhx4 与 Runx2 相互作用,Runx2 位于 Osterix 的上游。我们的研究结果表明,Zfhx4 协调了 Osterix 的转录网络,进而协调了软骨内骨化。