Department of Pathology, University of Cambridge, Tennis Court Road, Cambridge, CB21QP, United Kingdom.
Proc Natl Acad Sci U S A. 2011 Aug 30;108(35):14449-54. doi: 10.1073/pnas.1107666108. Epub 2011 Aug 15.
The WAVE regulatory complex (WRC) is a critical element in the control of actin polymerization at the eukaryotic cell membrane, but how WRC is activated remains uncertain. While Rho GTPase Rac1 can bind and activate WRC in vitro, this interaction is of low affinity, suggesting other factors may be important. By reconstituting WAVE-dependent actin assembly on membrane-coated beads in mammalian cell extracts, we found that Rac1 was not sufficient to engender bead motility, and we uncovered a key requirement for Arf GTPases. In vitro, Rac1 and Arf1 were individually able to bind weakly to recombinant WRC and activate it, but when both GTPases were bound at the membrane, recruitment and concomitant activation of WRC were dramatically enhanced. This cooperativity between the two GTPases was sufficient to induce WAVE-dependent bead motility in cell extracts. Our findings suggest that Arf GTPases may be central components in WAVE signalling, acting directly, alongside Rac1.
WAVE 调节复合物(WRC)是真核细胞膜中肌动蛋白聚合控制的关键要素,但 WRC 如何被激活仍不确定。虽然 Rho GTPase Rac1 可以在体外结合并激活 WRC,但这种相互作用亲和力较低,这表明其他因素可能很重要。通过在哺乳动物细胞提取物中用膜包被的珠粒上重新组装依赖于 WAVE 的肌动蛋白组装,我们发现 Rac1 不足以引起珠粒运动,并且我们发现了 Arf GTPases 的关键要求。在体外,Rac1 和 Arf1 都可以单独弱结合重组 WRC 并激活它,但当两种 GTPase 都在膜上结合时,WRC 的募集和伴随的激活显著增强。这两种 GTPase 之间的这种协同作用足以在细胞提取物中诱导依赖于 WAVE 的珠粒运动。我们的发现表明,Arf GTPases 可能是 WAVE 信号传导的核心组成部分,与 Rac1 直接作用。