Department of Biophysics and Howard Hughes Medical Institute, University of Texas Southwestern Medical Center at Dallas, 5323 Harry Hines Boulevard, Dallas, TX 75390, USA.
Institut für Neurobiologie, Universität Münster, 48149 Münster, Germany.
Cell. 2014 Jan 16;156(1-2):195-207. doi: 10.1016/j.cell.2013.11.048.
The WAVE regulatory complex (WRC) controls actin cytoskeletal dynamics throughout the cell by stimulating the actin-nucleating activity of the Arp2/3 complex at distinct membrane sites. However, the factors that recruit the WRC to specific locations remain poorly understood. Here, we have identified a large family of potential WRC ligands, consisting of ∼120 diverse membrane proteins, including protocadherins, ROBOs, netrin receptors, neuroligins, GPCRs, and channels. Structural, biochemical, and cellular studies reveal that a sequence motif that defines these ligands binds to a highly conserved interaction surface of the WRC formed by the Sra and Abi subunits. Mutating this binding surface in flies resulted in defects in actin cytoskeletal organization and egg morphology during oogenesis, leading to female sterility. Our findings directly link diverse membrane proteins to the WRC and actin cytoskeleton and have broad physiological and pathological ramifications in metazoans.
WAVE 调节复合物(WRC)通过在不同的膜位点刺激 Arp2/3 复合物的肌动蛋白成核活性来控制整个细胞中的肌动蛋白细胞骨架动态。然而,将 WRC 募集到特定位置的因素仍知之甚少。在这里,我们已经鉴定出一大类潜在的 WRC 配体,包括约 120 种不同的膜蛋白,包括原钙黏蛋白、ROBO 蛋白、轴突导向因子受体、神经连接蛋白、GPCR 蛋白和通道。结构、生化和细胞研究表明,定义这些配体的序列基序与由 Sra 和 Abi 亚基形成的 WRC 的高度保守相互作用表面结合。在果蝇中突变这个结合表面会导致卵子发生过程中肌动蛋白细胞骨架组织和卵子形态的缺陷,导致雌性不育。我们的发现将不同的膜蛋白直接与 WRC 和肌动蛋白细胞骨架联系起来,并在后生动物中有广泛的生理和病理意义。