Institut für Neurobiologie, Universität Münster, 48149 Münster, Germany.
Mol Biol Cell. 2011 Nov;22(21):4079-92. doi: 10.1091/mbc.E11-02-0121. Epub 2011 Sep 7.
A tight spatial-temporal coordination of F-actin dynamics is crucial for a large variety of cellular processes that shape cells. The Abelson interactor (Abi) has a conserved role in Arp2/3-dependent actin polymerization, regulating Wiskott-Aldrich syndrome protein (WASP) and WASP family verprolin-homologous protein (WAVE). In this paper, we report that Abi exerts nonautonomous control of photoreceptor axon targeting in the Drosophila visual system through WAVE. In abi mutants, WAVE is unstable but restored by reexpression of Abi, confirming that Abi controls the integrity of the WAVE complex in vivo. Remarkably, expression of a membrane-tethered WAVE protein rescues the axonal projection defects of abi mutants in the absence of the other subunits of the WAVE complex, whereas cytoplasmic WAVE only slightly affects the abi mutant phenotype. Thus complex formation not only stabilizes WAVE, but also provides further membrane-recruiting signals, resulting in an activation of WAVE.
F-肌动蛋白动力学的紧密时空协调对于塑造细胞的多种细胞过程至关重要。Abelson 相互作用蛋白 (Abi) 在 Arp2/3 依赖性肌动蛋白聚合中具有保守作用,调节 Wiskott-Aldrich 综合征蛋白 (WASP) 和 WASP 家族 verprolin 同源蛋白 (WAVE)。在本文中,我们报告 Abi 通过 WAVE 对果蝇视觉系统中的光感受器轴突靶向发挥非自主控制。在 abi 突变体中,WAVE 不稳定,但通过重新表达 Abi 得到恢复,这证实了 Abi 在体内控制 WAVE 复合物的完整性。值得注意的是,表达膜结合的 WAVE 蛋白可挽救 abi 突变体的轴突投射缺陷,而无需 WAVE 复合物的其他亚基,而细胞质 WAVE 仅略微影响 abi 突变体表型。因此,复合物的形成不仅稳定了 WAVE,而且还提供了进一步的膜募集信号,从而激活了 WAVE。