Division of Basic Sciences, Fred Hutchinson Cancer Research Center, 1100 Fairview Av., N. Seattle, WA 98109, USA.
Mech Dev. 2011 Jan-Feb;128(1-2):59-70. doi: 10.1016/j.mod.2010.10.001. Epub 2010 Nov 3.
Signaling through the Notch receptor has dramatically different effects depending on cell type and developmental timing. While a myriad of biological systems affected by Notch have been described, the molecular mechanisms by which a generic Notch signal is translated into a cell-type-specific output are less clear. Canonically, the Notch intracellular domain (NICD) translocates into the nucleus upon ligand binding to transcriptionally regulate target genes. In order to generate specificity, therefore, additional factors must exist that modulate NICD activity. Here we describe a novel regulator of the Notch pathway, Endonuclease GI (EndoGI). EndoGI localizes to the nucleus of most cells and activates Notch signaling when overexpressed. In the absence of endoGI, mutant animals are viable, but uncoordinated as motor neurons fail to innervate their appropriate muscle targets. Our data is therefore consistent with EndoGI functioning as a positive regulator of the Notch signaling pathway, playing a critical role during axon guidance of motor neurons.
Notch 受体的信号传递会根据细胞类型和发育时间而产生显著不同的影响。虽然已经描述了许多受 Notch 影响的生物系统,但将通用的 Notch 信号转化为细胞类型特异性输出的分子机制尚不清楚。通常情况下,配体结合后 Notch 细胞内结构域 (NICD) 会转位到细胞核,从而转录调控靶基因。因此,为了产生特异性,必须存在额外的调节 NICD 活性的因子。在这里,我们描述了 Notch 途径的一种新型调节因子内切核酸酶 GI(EndoGI)。EndoGI 定位于大多数细胞的细胞核中,并在过表达时激活 Notch 信号。在没有 endoGI 的情况下,突变动物是存活的,但由于运动神经元不能将其适当的肌肉靶标支配,因此不协调。因此,我们的数据表明 EndoGI 作为 Notch 信号通路的正调节剂发挥作用,在运动神经元的轴突导向中起着关键作用。