Yan Bo, Neilson Karen M, Moody Sally A
Department of Anatomy and Regenerative Biology, The George Washington University Medical Center, Washington, DC, USA.
Dev Dyn. 2009 Jun;238(6):1358-65. doi: 10.1002/dvdy.21885.
We investigated the role of the Notch signaling pathway in regulating several transcription factors that stabilize a neural fate and expand the neural plate. Increased Notch signaling in a neural lineage via a constitutively activated form (NICD) up-regulated geminin and zic2 in a cell-autonomous manner, and expanded the neural plate domains of sox11, sox2, and sox3. Loss- and gain-of-function assays show that foxD5 acts upstream of notch1 gene expression. Decreasing Notch signaling with an anti-morphic form of a Notch ligand (X-Delta-1(STU)) showed that the foxD5-mediated expansion of the sox gene neural plate domains requires Notch signaling. However, geminin and zic2 appear to be dually regulated by foxD5 and Notch1 signaling. These studies demonstrate that: (1) Notch signaling acts downstream of foxD5 to promote the expression of a subset of neural ectodermal transcription factors; and (2) Notch signaling and the foxD5 transcriptional pathway together maintain the neural plate in an undifferentiated state. Developmental Dynamics 238:1358-1365, 2009. (c) 2009 Wiley-Liss, Inc.
我们研究了Notch信号通路在调控几种稳定神经命运并扩展神经板的转录因子中的作用。通过组成型激活形式(NICD)在神经谱系中增加Notch信号,以细胞自主方式上调双微体蛋白(geminin)和锌指蛋白2(zic2),并扩展了性别决定区Y框蛋白11(sox11)、性别决定区Y框蛋白2(sox2)和性别决定区Y框蛋白3(sox3)的神经板结构域。功能缺失和功能获得实验表明,叉头框D5(foxD5)在Notch1基因表达的上游起作用。用Notch配体的反式形态(X - Delta - 1(STU))降低Notch信号,结果显示foxD5介导的sox基因神经板结构域的扩展需要Notch信号。然而,双微体蛋白和锌指蛋白2似乎受foxD5和Notch1信号的双重调控。这些研究表明:(1)Notch信号在foxD5的下游起作用,以促进神经外胚层转录因子子集的表达;(2)Notch信号和foxD5转录途径共同维持神经板处于未分化状态。《发育动力学》238:1358 - 1365,2009年。(c)2009年威利 - 利斯出版公司。