Gu Ying, Fu Ying, Dowd Peter, Li Shundai, Vernoud Vanessa, Gilroy Simon, Yang Zhenbiao
Center for Plant Cell Biology, Institute for Integrative Genome Biology, Department of Botany and Plant Sciences, University of California, Riverside 92521, USA.
J Cell Biol. 2005 Apr 11;169(1):127-38. doi: 10.1083/jcb.200409140.
Tip growth in neuronal cells, plant cells, and fungal hyphae is known to require tip-localized Rho GTPase, calcium, and filamentous actin (F-actin), but how they interact with each other is unclear. The pollen tube is an exciting model to study spatiotemporal regulation of tip growth and F-actin dynamics. An Arabidopsis thaliana Rho family GTPase, ROP1, controls pollen tube growth by regulating apical F-actin dynamics. This paper shows that ROP1 activates two counteracting pathways involving the direct targets of tip-localized ROP1: RIC3 and RIC4. RIC4 promotes F-actin assembly, whereas RIC3 activates Ca(2+) signaling that leads to F-actin disassembly. Overproduction or depletion of either RIC4 or RIC3 causes tip growth defects that are rescued by overproduction or depletion of RIC3 or RIC4, respectively. Thus, ROP1 controls actin dynamics and tip growth through a check and balance between the two pathways. The dual and antagonistic roles of this GTPase may provide a unifying mechanism by which Rho modulates various processes dependent on actin dynamics in eukaryotic cells.
已知神经元细胞、植物细胞和真菌菌丝的顶端生长需要顶端定位的Rho GTP酶、钙和丝状肌动蛋白(F-肌动蛋白),但它们之间如何相互作用尚不清楚。花粉管是研究顶端生长和F-肌动蛋白动力学时空调控的一个令人兴奋的模型。拟南芥Rho家族GTP酶ROP1通过调节顶端F-肌动蛋白动力学来控制花粉管生长。本文表明,ROP1激活了两条相互拮抗的途径,涉及顶端定位的ROP1的直接靶点:RIC3和RIC4。RIC4促进F-肌动蛋白组装,而RIC3激活导致F-肌动蛋白解聚的Ca(2+)信号。过量表达或缺失RIC4或RIC3都会导致顶端生长缺陷,分别通过过量表达或缺失RIC3或RIC4得以挽救。因此,ROP1通过两条途径之间的制衡来控制肌动蛋白动力学和顶端生长。这种GTP酶的双重和拮抗作用可能提供了一种统一的机制,通过该机制Rho调节真核细胞中依赖于肌动蛋白动力学的各种过程。