Graduate School of Biological Sciences, Nara Institute of Science and Technology, Ikoma 630-0192, Japan.
Nat Cell Biol. 2010 Nov;12(11):1064-70. doi: 10.1038/ncb2110. Epub 2010 Oct 10.
Microtubule nucleation in interphase plant cells primarily occurs through branching from pre-existing microtubules at dispersed sites in the cell cortex. The minus ends of new microtubules are often released from the sites of nucleation, and the free microtubules are then transported to new locations by polymer treadmilling. These nucleation-and-release events are characteristic features of plant arrays in interphase cells, but little is known about the spatiotemporal control of these events by nucleating protein complexes. We visualized the dynamics of two fluorescently-tagged γ-tubulin complex proteins, GCP2 and GCP3, in Arabidopsis thaliana. These probes labelled motile complexes in the cytosol that transiently stabilized at fixed locations in the cell cortex. Recruitment of labelled complexes occurred preferentially along existing cortical microtubules, from which new microtubule was synthesized in a branching manner, or in parallel to the existing microtubule. Complexes localized to microtubules were approximately 10-fold more likely to display nucleation than were complexes recruited to other locations. Nucleating complexes remained stable until daughter microtubules were either completely depolymerized from their plus ends or released by katanin-dependent severing activity. These observations suggest that the nucleation complexes are primarily activated on association with microtubule lattices, and that nucleation complex stability depends on association with daughter microtubules and is regulated in part by katanin activity.
在间期植物细胞中,微管的成核主要通过在细胞皮层的离散位点上从预先存在的微管分支发生。新微管的负端通常从成核位点释放出来,然后游离的微管通过聚合 treadmilling 被运输到新的位置。这些成核和释放事件是间期细胞中植物微管阵列的特征,但对于成核蛋白复合物对这些事件的时空控制知之甚少。我们在拟南芥中可视化了两个荧光标记的 γ-微管蛋白复合物蛋白 GCP2 和 GCP3 的动力学。这些探针标记了细胞质中的可移动复合物,这些复合物在细胞皮层的固定位置短暂稳定。标记复合物的募集优先发生在现有的皮层微管上,从这些微管上以分支的方式合成新的微管,或者与现有的微管平行。定位于微管上的复合物显示出成核的可能性大约是被招募到其他位置的复合物的 10 倍。成核复合物保持稳定,直到子微管从其正端完全解聚或被 katain 依赖性切割活性释放。这些观察结果表明,成核复合物主要在与微管晶格结合时被激活,并且成核复合物的稳定性取决于与子微管的结合,并部分受 katain 活性的调节。