Hable Whitney E, Reddy Sriharshan, Julien Lindsay
Department of Biology, University of Massachusetts Dartmouth, North Dartmouth, MA 02747-2300, USA.
Planta. 2008 Apr;227(5):991-1000. doi: 10.1007/s00425-007-0673-1. Epub 2008 Jan 9.
Proper cell morphogenesis is dependent on the establishment and expression of cellular polarity. In the fucoid zygote, cell shape is critical for establishing the developmental pattern of the adult, and is achieved by guiding insertion of new membrane and wall to the rhizoid tip. Selection and growth of the appropriate tip site are accompanied by formation of dynamic actin arrays associated with the actin-nucleating Arp2/3 complex. In eukaryotes, a major pathway for activation of the Arp2/3 complex is via the Rho family GTPase, Rac1, which stimulates the Scar/WAVE complex. To determine whether Rac1 controls actin nucleation in Silvetia compressa (J. Agardh) E. Serrao, T. O. Cho, S. M. Boo et Brawley, we tested the effects of the Rac1-specific inhibitory compound, NSC23766, on actin dependent processes and on actin arrays. We found that NSC23766 disrupted polar secretion of adhesive, polarization of endomembranes, and tip-focused growth in the rhizoid. Similarly, NSC23766 altered actin and Arp2 localization in the growing rhizoid. In contrast, NSC23766 had no effect on selection of the growth site or on cytokinesis. These data suggest that Rac1 participates in nucleation of specific actin arrays in the developing zygote.
正确的细胞形态发生依赖于细胞极性的建立和表达。在岩藻合子中,细胞形状对于确立成体的发育模式至关重要,并且通过引导新的膜和细胞壁插入到假根尖端来实现。合适尖端位点的选择和生长伴随着与肌动蛋白成核的Arp2/3复合体相关的动态肌动蛋白阵列的形成。在真核生物中,激活Arp2/3复合体的主要途径是通过Rho家族GTP酶Rac1,它刺激Scar/WAVE复合体。为了确定Rac1是否控制压缩鹿角菜(J. Agardh)E. Serrao、T. O. Cho、S. M. Boo和Brawley中的肌动蛋白成核,我们测试了Rac1特异性抑制化合物NSC23766对肌动蛋白依赖性过程和肌动蛋白阵列的影响。我们发现NSC23766破坏了黏附分子的极性分泌、内膜的极化以及假根中的尖端聚焦生长。同样,NSC23766改变了生长中的假根中肌动蛋白和Arp2的定位。相比之下,NSC23766对生长位点的选择或胞质分裂没有影响。这些数据表明Rac1参与了发育中的合子中特定肌动蛋白阵列的成核。