Cell Biology, Department of Biology, Faculty of Science, Utrecht University, 3584 Utrecht, The Netherlands; email:
Annu Rev Cell Dev Biol. 2017 Oct 6;33:51-75. doi: 10.1146/annurev-cellbio-100616-060615. Epub 2017 Jun 23.
The organization of microtubule networks is crucial for controlling chromosome segregation during cell division, for positioning and transport of different organelles, and for cell polarity and morphogenesis. The geometry of microtubule arrays strongly depends on the localization and activity of the sites where microtubules are nucleated and where their minus ends are anchored. Such sites are often clustered into structures known as microtubule-organizing centers, which include the centrosomes in animals and spindle pole bodies in fungi. In addition, other microtubules, as well as membrane compartments such as the cell nucleus, the Golgi apparatus, and the cell cortex, can nucleate, stabilize, and tether microtubule minus ends. These activities depend on microtubule-nucleating factors, such as γ-tubulin-containing complexes and their activators and receptors, and microtubule minus end-stabilizing proteins with their binding partners. Here, we provide an overview of the current knowledge on how such factors work together to control microtubule organization in different systems.
微管网络的组织对于控制细胞分裂过程中的染色体分离、不同细胞器的定位和运输以及细胞极性和形态发生至关重要。微管阵列的几何形状强烈依赖于微管起始和微管负端锚定的位点的定位和活性。这些位点通常聚集形成称为微管组织中心的结构,其中包括动物中的中心体和真菌中的纺锤体极体。此外,其他微管以及膜隔室,如细胞核、高尔基体和细胞皮质,也可以起始、稳定和固定微管负端。这些活性取决于微管起始因子,如含有γ-微管蛋白的复合物及其激活剂和受体,以及微管负端稳定蛋白及其结合伴侣。在这里,我们概述了目前关于这些因子如何协同作用以控制不同系统中微管组织的知识。