Klahre Ulrich, Kost Benedikt
Heidelberg Institute of Plant Sciences, University of Heidelberg, 69120 Heidelberg, Germany.
Plant Cell. 2006 Nov;18(11):3033-46. doi: 10.1105/tpc.106.045336. Epub 2006 Nov 10.
Regulation by Rho-type small GTPases, such as RAC5, is important for the maintenance of polarity in tobacco (Nicotiana tabacum) pollen tubes. We previously showed that RhoGDI2 is necessary for RAC5 localization. Here, we describe the GTPase activating protein RhoGAP1 that controls the area of RAC5 activity. RhoGAP1 N-terminal and CRIB (for Cdc42/Rac-interactive binding) domains are both necessary for targeting yellow fluorescent protein-RhoGAP1 fusions to the plasma membrane close to, but not in, pollen tube apices. We propose that this localization restricts apical Rho-type GTPase activity from spreading toward the flanks, which ensures the maintenance of RAC signaling at the apex. The CRIB domain is not required but enhances in vitro RhoGAP1 activity toward the pollen tube-specific-RAC5. A mutation reducing GAP activity of RhoGAP1 leads to ballooning pollen tubes resembling those overexpressing RAC5. To ascertain the specific targeting mechanism of RhoGAP1, we isolated a 14-3-3 protein interacting with RhoGAP1. When overexpressed with RhoGAP1, it counteracts the growth-retarding effect of RhoGAP1 overexpression and attenuates RhoGAP1 membrane localization but, overexpressed alone, induces only small architectural changes. We propose that inactivation of RAC5 by the subapically localized RhoGAP1, together with dynamic relocalization of inactivated RAC5 from flanks to tip by RhoGDI2, leads to spatial restriction of RAC5 to pollen tube apices, thereby sustaining polar growth.
诸如RAC5之类的Rho型小GTP酶的调控对于烟草(Nicotiana tabacum)花粉管极性的维持很重要。我们之前表明RhoGDI2对于RAC5的定位是必需的。在此,我们描述了控制RAC5活性区域的GTP酶激活蛋白RhoGAP1。RhoGAP1的N端和CRIB(用于Cdc42/Rac相互作用结合)结构域对于将黄色荧光蛋白-RhoGAP1融合蛋白靶向到靠近但不在花粉管顶端的质膜都是必需的。我们提出这种定位限制了顶端Rho型GTP酶活性向侧翼扩散,从而确保顶端RAC信号的维持。CRIB结构域不是必需的,但能增强体外RhoGAP1对花粉管特异性RAC5的活性。降低RhoGAP1的GAP活性的突变会导致花粉管膨胀,类似于过表达RAC5的花粉管。为了确定RhoGAP1的特定靶向机制,我们分离出了一种与RhoGAP1相互作用的14-3-3蛋白。当与RhoGAP1一起过表达时,它会抵消RhoGAP1过表达的生长抑制作用并减弱RhoGAP1的膜定位,但单独过表达时,只会引起微小的结构变化。我们提出,由亚顶端定位的RhoGAP1使RAC5失活,以及通过RhoGDI2使失活的RAC5从侧翼动态重新定位到顶端,导致RAC5在花粉管顶端的空间限制,从而维持极性生长。