Pacquelet A, Zanin E, Ashiono C, Gotta M
ETH Zurich, Institute of Biochemistry, Schafmattstrasse 18, 8093 Zurich, Switzerland.
Dev Biol. 2008 Jul 15;319(2):267-72. doi: 10.1016/j.ydbio.2008.04.016. Epub 2008 Apr 23.
The PAR proteins have an essential and conserved function in establishing polarity in many cell types and organisms. However, their key upstream regulators remain to be identified. In C. elegans, regulators of the PAR proteins can be identified by their ability to suppress the lethality of par-2 mutant embryos. Here we show that a nos-3 loss of function mutant suppresses the lethality of par-2 mutants by regulating PAR-6 protein levels. The suppression requires the activity of the sex determination genes fem-1/2/3 and of the cullin cul-2. FEM-1 is a substrate-specific adaptor for a CUL-2-based ubiquitin ligase (CBC(FEM-1)). Interestingly, we find that CUL-2 is required for the regulation of PAR-6 levels and that PAR-6 physically interacts with FEM-1. Our data strongly suggest that PAR-6 levels are regulated by the CBC(FEM-1) ubiquitin ligase thereby uncovering a novel role for the FEM proteins and cullin-dependent degradation in regulating PAR proteins and polarity processes.
PAR蛋白在许多细胞类型和生物体中建立极性方面具有重要且保守的功能。然而,它们的关键上游调节因子仍有待确定。在秀丽隐杆线虫中,PAR蛋白的调节因子可通过其抑制par-2突变胚胎致死性的能力来鉴定。在这里,我们表明nos-3功能缺失突变体通过调节PAR-6蛋白水平来抑制par-2突变体的致死性。这种抑制作用需要性别决定基因fem-1/2/3和cullin cul-2的活性。FEM-1是基于CUL-2的泛素连接酶(CBC(FEM-1))的底物特异性衔接蛋白。有趣的是,我们发现CUL-2是调节PAR-6水平所必需的,并且PAR-6与FEM-1发生物理相互作用。我们的数据强烈表明,PAR-6水平受CBC(FEM-1)泛素连接酶调节,从而揭示了FEM蛋白和cullin依赖性降解在调节PAR蛋白和极性过程中的新作用。