Zhou Zhenzhen, Shi Haifan, Chen Binqing, Zhang Ruihui, Huang Shanjin, Fu Ying
State Key Laboratory of Plant Physiology and Biochemistry, College of Biological Sciences, China Agricultural University, Beijing 100193, China.
Key Laboratory of Plant Molecular Physiology, Institute of Botany, Chinese Academy of Sciences, Beijing 100093, China.
Plant Cell. 2015 Apr;27(4):1140-61. doi: 10.1105/tpc.114.135400. Epub 2015 Mar 24.
Pollen tubes deliver sperms to the ovule for fertilization via tip growth. The rapid turnover of F-actin in pollen tube tips plays an important role in this process. In this study, we demonstrate that Arabidopsis thaliana RIC1, a member of the ROP-interactive CRIB motif-containing protein family, regulates pollen tube growth via its F-actin severing activity. Knockout of RIC1 enhanced pollen tube elongation, while overexpression of RIC1 dramatically reduced tube growth. Pharmacological analysis indicated that RIC1 affected F-actin dynamics in pollen tubes. In vitro biochemical assays revealed that RIC1 directly bound and severed F-actin in the presence of Ca(2+) in addition to interfering with F-actin turnover by capping F-actin at the barbed ends. In vivo, RIC1 localized primarily to the apical plasma membrane (PM) of pollen tubes. The level of RIC1 at the apical PM oscillated during pollen tube growth. The frequency of F-actin severing at the apex was notably decreased in ric1-1 pollen tubes but was increased in pollen tubes overexpressing RIC1. We propose that RIC1 regulates F-actin dynamics at the apical PM as well as the cytosol by severing F-actin and capping the barbed ends in the cytoplasm, establishing a novel mechanism that underlies the regulation of pollen tube growth.
花粉管通过顶端生长将精子输送到胚珠进行受精。花粉管顶端F-肌动蛋白的快速周转在这一过程中起着重要作用。在本研究中,我们证明拟南芥RIC1(一种含ROP相互作用CRIB基序的蛋白家族成员)通过其F-肌动蛋白切割活性调节花粉管生长。RIC1基因敲除增强了花粉管的伸长,而RIC1的过表达则显著降低了花粉管的生长。药理学分析表明,RIC1影响花粉管中F-肌动蛋白的动态变化。体外生化分析显示,RIC1在Ca(2+)存在的情况下直接结合并切割F-肌动蛋白,此外还通过在肌动蛋白丝的带刺末端封端来干扰F-肌动蛋白的周转。在体内,RIC1主要定位于花粉管的顶端质膜(PM)。在花粉管生长过程中,顶端质膜上的RIC1水平会发生波动。在ric1-1花粉管中,顶端F-肌动蛋白的切割频率显著降低,但在过表达RIC1的花粉管中则增加。我们提出,RIC1通过切割F-肌动蛋白并在细胞质中封端带刺末端来调节顶端质膜以及细胞质中的F-肌动蛋白动态变化,从而建立了一种调节花粉管生长的新机制。