Université Paris Sud, Centre Universitaire, F-91405 Orsay, France; Institut Curie, CNRS UMR3347, INSERM U1021, Centre Universitaire, F-91405 Orsay, France.
University of California at Berkeley, Department of Molecular and Cell Biology and Center for Integrative Genomics, USA.
Dev Biol. 2014 Feb 15;386(2):461-72. doi: 10.1016/j.ydbio.2013.12.010. Epub 2013 Dec 17.
Neural crest development is orchestrated by a complex and still poorly understood gene regulatory network. Premigratory neural crest is induced at the lateral border of the neural plate by the combined action of signaling molecules and transcription factors such as AP2, Gbx2, Pax3 and Zic1. Among them, Pax3 and Zic1 are both necessary and sufficient to trigger a complete neural crest developmental program. However, their gene targets in the neural crest regulatory network remain unknown. Here, through a transcriptome analysis of frog microdissected neural border, we identified an extended gene signature for the premigratory neural crest, and we defined novel potential members of the regulatory network. This signature includes 34 novel genes, as well as 44 known genes expressed at the neural border. Using another microarray analysis which combined Pax3 and Zic1 gain-of-function and protein translation blockade, we uncovered 25 Pax3 and Zic1 direct targets within this signature. We demonstrated that the neural border specifiers Pax3 and Zic1 are direct upstream regulators of neural crest specifiers Snail1/2, Foxd3, Twist1, and Tfap2b. In addition, they may modulate the transcriptional output of multiple signaling pathways involved in neural crest development (Wnt, Retinoic Acid) through the induction of key pathway regulators (Axin2 and Cyp26c1). We also found that Pax3 could maintain its own expression through a positive autoregulatory feedback loop. These hierarchical inductions, feedback loops, and pathway modulations provide novel tools to understand the neural crest induction network.
神经嵴的发育是由一个复杂且尚未完全理解的基因调控网络所调控的。迁移前的神经嵴由神经板的侧向边界处的信号分子和转录因子(如 AP2、Gbx2、Pax3 和 Zic1)的共同作用诱导产生。其中,Pax3 和 Zic1 都是触发完整的神经嵴发育程序所必需和充分的。然而,它们在神经嵴调控网络中的基因靶标仍然未知。在这里,通过对青蛙微分离神经边界的转录组分析,我们确定了一个扩展的迁移前神经嵴的基因特征,并定义了调控网络的新的潜在成员。这个特征包括 34 个新基因,以及 44 个在神经边界表达的已知基因。我们利用另一个微阵列分析,该分析结合了 Pax3 和 Zic1 的功能获得和蛋白质翻译阻断,我们在这个特征中发现了 25 个 Pax3 和 Zic1 的直接靶标。我们证明,神经边界指定因子 Pax3 和 Zic1 是神经嵴指定因子 Snail1/2、Foxd3、Twist1 和 Tfap2b 的直接上游调控因子。此外,它们可能通过诱导关键信号通路调节因子(Axin2 和 Cyp26c1)来调节参与神经嵴发育的多个信号通路(Wnt、视黄酸)的转录输出。我们还发现 Pax3 可以通过正反馈环来维持自身的表达。这些层次诱导、反馈环和通路调节为理解神经嵴诱导网络提供了新的工具。