Gu X, Verma D P
Department of Molecular Genetics, Ohio State University, Columbus 43210, USA.
Plant Cell. 1997 Feb;9(2):157-69. doi: 10.1105/tpc.9.2.157.
The cell plate is formed by the fusion of Golgi apparatus-derived vesicles in the center of the phragmoplast during cytokinesis in plant cells. A dynamin-like protein, phragmoplastin, has been isolated and shown to be associated with cell plate formation in soybean by using immunocytochemistry. In this article, we demonstrate that similar to dynamin, phragmoplastin polymerizes to form oligomers. We fused soybean phragmoplastin with the green fluorescence protein (GFP) and introduced it into tobacco BY-2 cells to monitor the dynamics of early events in cell plate formation. We demonstrate that the chimeric protein is functional and targeted to the cell plate during cytokinesis in transgenic cells. GFP-phragmoplastin was found to appear first in the center of the forming cell plate, and as the cell plate grew outward, it redistributed to the growing margins of the cell plate. The redistribution of phragmoplastin may require microtubule reorganization because the microtubule-stabilizing drug taxol inhibited phragmoplastin redistribution. Our data show that throughout the entire process of cytokinesis, phragmoplastin is concentrated in the area in which membrane fusion is active, suggesting that phragmoplastin participates in an early membrane fusion event during cell plate formation. Based on the dynamics of GFP-phragmoplastin, it appears that the process of cell plate formation is completed in two phases. The first phase is confined to the cylinder of the phragmoplast proper and is followed by a second phase that deposits phragmoplast vesicles in a concentric fashion, resulting in a ring of fluorescence, with the concentration of vesicles being higher at the periphery. In addition, overexpression of GFP-phragmoplastin appears to act as a dominant negative, slowing down the completion of cell plate formation, and often results in an oblique cell plate. The latter appears to uncouple cell elongation from the plane of cell division, forming twisted and elongated cells with longitudinal cell divisions.
在植物细胞胞质分裂过程中,细胞板是由高尔基体衍生的小泡在成膜体中央融合形成的。一种类发动蛋白,成膜体蛋白,已被分离出来,并通过免疫细胞化学方法证明其与大豆细胞板的形成有关。在本文中,我们证明成膜体蛋白与发动蛋白类似,能够聚合形成寡聚体。我们将大豆成膜体蛋白与绿色荧光蛋白(GFP)融合,并将其导入烟草BY-2细胞,以监测细胞板形成早期事件的动态变化。我们证明这种嵌合蛋白具有功能,并且在转基因细胞的胞质分裂过程中靶向定位到细胞板。发现GFP-成膜体蛋白首先出现在正在形成的细胞板中央,随着细胞板向外生长,它重新分布到细胞板生长的边缘。成膜体蛋白的重新分布可能需要微管重组,因为微管稳定药物紫杉醇抑制了成膜体蛋白的重新分布。我们的数据表明,在胞质分裂的整个过程中,成膜体蛋白集中在膜融合活跃的区域,这表明成膜体蛋白参与了细胞板形成过程中的早期膜融合事件。基于GFP-成膜体蛋白的动态变化,细胞板的形成过程似乎分两个阶段完成。第一阶段局限于成膜体本身的柱状区域,随后是第二阶段,以同心方式沉积成膜体小泡,形成荧光环,小泡在外围的浓度更高。此外,GFP-成膜体蛋白的过表达似乎起到了显性负效应,减缓了细胞板形成的完成,并且常常导致倾斜的细胞板。后者似乎使细胞伸长与细胞分裂平面解偶联,形成具有纵向细胞分裂的扭曲和伸长的细胞。