Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Dev Cell. 2015 Sep 14;34(5):544-54. doi: 10.1016/j.devcel.2015.06.024. Epub 2015 Aug 6.
Neural crest cells are induced at the neural plate border by the combined action of transcription factors and signaling molecules. Here, we show that Axud1, a downstream effector of Wnt signaling, represents a critical missing link that integrates signaling and transcriptional cues to mediate neural crest formation. Axud1 is a transcription factor expressed in neural crest progenitors in a Wnt1/β-catenin-dependent manner. Axud1 loss leads to downregulation of multiple genes involved in neural crest specification, similar to the effects of Wnt1 knockdown. Importantly, Axud1 is sufficient to rescue neural crest formation after disruption of Wnt signaling. Furthermore, it physically interacts with neural plate border genes Pax7 and Msx1 in vivo to directly activate transcription of stem cell factor FoxD3, initiating the neural crest program. Thus, Axud1 integrates Wnt signaling with transcriptional inputs to endow the neural crest with its unique molecular signature.
神经嵴细胞由转录因子和信号分子的共同作用在神经板边缘诱导产生。在这里,我们表明,Wnt 信号的下游效应物 Axud1 代表了一个关键的缺失环节,它整合了信号和转录线索,介导神经嵴形成。Axud1 是一种转录因子,以 Wnt1/β-连环蛋白依赖的方式在神经嵴祖细胞中表达。Axud1 的缺失导致多个参与神经嵴特化的基因下调,这与 Wnt1 敲低的效果相似。重要的是,Axud1 在 Wnt 信号中断后足以挽救神经嵴的形成。此外,它在体内与神经板边界基因 Pax7 和 Msx1 相互作用,直接激活干细胞因子 FoxD3 的转录,启动神经嵴程序。因此,Axud1 将 Wnt 信号与转录输入相结合,赋予神经嵴独特的分子特征。