Han Ji W, Leeper Laura, Rivero Francisco, Chung Chang Y
Department of Pharmacology, Vanderbilt University Medical Center, Nashville, Tennessee 37232-6600, USA.
J Biol Chem. 2006 Nov 17;281(46):35224-34. doi: 10.1074/jbc.M605997200. Epub 2006 Sep 12.
WASP family proteins are key players for connecting multiple signaling pathways to F-actin polymerization. To dissect the highly integrated signaling pathways controlling WASP activity, we identified a Rac protein that binds to the GTPase binding domain of WASP. Using two-hybrid and FRET-based functional assays, we identified RacC as a major regulator of WASP. RacC stimulates F-actin assembly in cell-free systems in a WASP-dependent manner. A FRET-based microscopy approach showed local activation of RacC at the leading edge of chemotaxing cells. Cells overexpressing RacC exhibit a significant increase in the level of F-actin polymerization upon cAMP stimulation, which can be blocked by a phosphatidylinositol (PI) 3-kinase inhibitor. Membrane translocation of PI 3-kinase and PI 3,4,5-trisphosphate reporter is absent in racC null cells. Cells overexpressing dominant negative RacC mutants and racC null cells move at a significantly slower speed and show a poor directionality during chemotaxis. Our results suggest that RacC plays an important role in PI 3-kinase activation and WASP activation for dynamic regulation of F-actin assembly during Dictyostelium chemotaxis.
WASP家族蛋白是将多条信号通路与F-肌动蛋白聚合相连接的关键因子。为了剖析控制WASP活性的高度整合的信号通路,我们鉴定出一种与WASP的GTP酶结合结构域结合的Rac蛋白。利用双杂交和基于荧光共振能量转移(FRET)的功能分析,我们确定RacC是WASP的主要调节因子。RacC以WASP依赖的方式在无细胞体系中刺激F-肌动蛋白组装。一种基于FRET的显微镜方法显示趋化细胞前缘的RacC发生局部激活。过表达RacC的细胞在cAMP刺激后F-肌动蛋白聚合水平显著增加,这可被磷脂酰肌醇(PI)3-激酶抑制剂阻断。在racC基因敲除细胞中不存在PI 3-激酶和PI 3,4,5-三磷酸报告基因的膜转位。过表达显性负性RacC突变体的细胞和racC基因敲除细胞在趋化过程中移动速度显著减慢且方向性较差。我们的结果表明,在盘基网柄菌趋化过程中,RacC在PI 3-激酶激活和WASP激活中发挥重要作用,以动态调节F-肌动蛋白组装。