Nguyen Vân, Chokas Ann L, Stecca Barbara, Ruiz i Altaba Ariel
Department of Genetic Medicine and Development, 8242 CMU, 1 rue Michel Servet, University of Geneva Medical School, 1211 Geneva 4, Switzerland.
Development. 2005 Jul;132(14):3267-79. doi: 10.1242/dev.01905.
The Gli proteins are critical components of multiple processes in development, homeostasis and disease, including neurogenesis and tumorigenesis. However, it is unclear how the Gli code, the sum of their combinatorial positive and negative functions, dictates cell fate and behavior. Using an antisense approach to knockdown gene function in vivo, we find that each of the three Gli proteins is required for the induction of all primary neurons in the amphibian neural plate and regulates the bHLH/Notch neurogenic cascade. Analyses of endogenous Gli function in Gli-mediated neurogenesis and tumorigenesis, and in animal cap assays, reveal specific requirements that are context specific. Nuclear colocalization and binding studies suggest the formation of complexes, with the first two zinc fingers of the Gli five zinc-finger domain acting as a protein-protein interaction site. The Gli proteins therefore appear to form a dynamic physical network that underlies cooperative function, greatly extending the combinatorial possibilities of the Gli code, which may be further fine-tuned in cell fate specification by co-factor function.
Gli蛋白是发育、体内平衡和疾病(包括神经发生和肿瘤发生)中多个过程的关键组成部分。然而,尚不清楚Gli编码(其组合的正负功能之和)如何决定细胞命运和行为。通过体内反义方法敲低基因功能,我们发现三种Gli蛋白中的每一种都是两栖动物神经板中所有初级神经元诱导所必需的,并调节bHLH/Notch神经发生级联反应。对Gli介导的神经发生和肿瘤发生以及动物帽实验中内源性Gli功能的分析揭示了特定背景下的特定要求。核共定位和结合研究表明形成了复合物,Gli五个锌指结构域的前两个锌指作为蛋白质-蛋白质相互作用位点。因此,Gli蛋白似乎形成了一个动态的物理网络,作为协同功能的基础,极大地扩展了Gli编码的组合可能性,这可能在细胞命运特化中通过辅助因子功能进一步微调。