Qin Tao, Liu Xiaomin, Li Jiejie, Sun Jingbo, Song Leina, Mao Tonglin
State Key Laboratory of Plant Physiology and Biochemistry, Department of Plant Sciences, College of Biological Sciences, China Agricultural University, Beijing 100193, China.
Plant Cell. 2014 Jan;26(1):325-39. doi: 10.1105/tpc.113.119768. Epub 2014 Jan 14.
The formation of distinct actin filament arrays in the subapical region of pollen tubes is crucial for pollen tube growth. However, the molecular mechanisms underlying the organization and dynamics of the actin filaments in this region remain to be determined. This study shows that Arabidopsis thaliana MICROTUBULE-DESTABILIZING PROTEIN25 (MDP25) has the actin filament-severing activity of an actin binding protein. This protein negatively regulated pollen tube growth by modulating the organization and dynamics of actin filaments in the subapical region of pollen tubes. MDP25 loss of function resulted in enhanced pollen tube elongation and inefficient fertilization. MDP25 bound directly to actin filaments and severed individual actin filaments, in a manner that was dramatically enhanced by Ca(2+), in vitro. Analysis of a mutant that bears a point mutation at the Ca(2+) binding sites demonstrated that the subcellular localization of MDP25 was determined by cytosolic Ca(2+) level in the subapical region of pollen tubes, where MDP25 was disassociated from the plasma membrane and moved into the cytosol. Time-lapse analysis showed that the F-actin-severing frequency significantly decreased and a high density of actin filaments was observed in the subapical region of mdp25-1 pollen tubes. This study reveals a mechanism whereby calcium enhances the actin filament-severing activity of MDP25 in the subapical region of pollen tubes to modulate pollen tube growth.
花粉管亚顶端区域形成独特的肌动蛋白丝阵列对花粉管生长至关重要。然而,该区域肌动蛋白丝的组织和动态变化的分子机制仍有待确定。本研究表明,拟南芥微管去稳定蛋白25(MDP25)具有肌动蛋白结合蛋白的肌动蛋白丝切断活性。该蛋白通过调节花粉管亚顶端区域肌动蛋白丝的组织和动态变化来负调控花粉管生长。MDP25功能缺失导致花粉管伸长增强和受精效率低下。在体外,MDP25直接与肌动蛋白丝结合并切断单根肌动蛋白丝,这种作用在Ca(2+)存在时显著增强。对在Ca(2+)结合位点发生点突变的突变体分析表明,MDP25的亚细胞定位由花粉管亚顶端区域的胞质Ca(2+)水平决定,在该区域MDP25从质膜解离并进入胞质溶胶。延时分析表明,mdp25-1花粉管亚顶端区域的F-肌动蛋白切断频率显著降低,且观察到高密度的肌动蛋白丝。本研究揭示了一种机制,即钙增强花粉管亚顶端区域MDP25的肌动蛋白丝切断活性以调节花粉管生长。