Center for Craniofacial Molecular Biology, University of Southern California, Los Angeles, CA 90033, USA; Department of Prosthodontics, Shanghai Ninth People's Hospital, College of Stomatology, Shanghai Jiao Tong University School of Medicine, Shanghai 200011, China.
Center for Craniofacial Molecular Biology, University of Southern California, Los Angeles, CA 90033, USA.
Cell Rep. 2021 Apr 6;35(1):108964. doi: 10.1016/j.celrep.2021.108964.
Chromatin remodelers often show broad expression patterns in multiple cell types yet can elicit cell-specific effects in development and diseases. Arid1a binds DNA and regulates gene expression during tissue development and homeostasis. However, it is unclear how Arid1a achieves its functional specificity in regulating progenitor cells. Using the tooth root as a model, we show that loss of Arid1a impairs the differentiation-associated cell cycle arrest of tooth root progenitors through Hedgehog (Hh) signaling regulation, leading to shortened roots. Our data suggest that Plagl1, as a co-factor, endows Arid1a with its cell-type/spatial functional specificity. Furthermore, we show that loss of Arid1a leads to increased expression of Arid1b, which is also indispensable for odontoblast differentiation but is not involved in regulation of Hh signaling. This study expands our knowledge of the intricate interactions among chromatin remodelers, transcription factors, and signaling molecules during progenitor cell fate determination and lineage commitment.
染色质重塑因子在多种细胞类型中通常表现出广泛的表达模式,但在发育和疾病中可以引发细胞特异性效应。ARID1A 结合 DNA 并在组织发育和稳态过程中调节基因表达。然而,ARID1A 如何在调节祖细胞方面实现其功能特异性尚不清楚。我们以牙根作为模型,表明 ARID1A 的缺失通过 Hedgehog(Hh)信号调节损害了牙根祖细胞的分化相关细胞周期阻滞,导致牙根缩短。我们的数据表明,PLAGL1 作为共因子赋予 ARID1A 细胞类型/空间功能特异性。此外,我们表明 ARID1A 的缺失导致 ARID1B 的表达增加,ARID1B 对于成牙本质细胞分化也是必不可少的,但不参与 Hh 信号调节。这项研究扩展了我们对染色质重塑因子、转录因子和信号分子在祖细胞命运决定和谱系承诺过程中复杂相互作用的认识。