Department of Molecular and Cell Biology, University of California, Berkeley, CA 94720, USA.
Department of Molecular and Cell Biology, University of California, Berkeley, CA 94720, USA
J Cell Sci. 2018 Sep 24;132(4):jcs219386. doi: 10.1242/jcs.219386.
Microtubules (MTs) are important for cellular structure, transport of cargoes and segregation of chromosomes and organelles during mitosis. The stochastic growth and shrinkage of MTs, known as dynamic instability, is necessary for these functions. Previous studies to determine how individual MT-associated proteins (MAPs) affect MT dynamics have been performed either through studies, which provide limited opportunity for observation of individual MTs or manipulation of conditions, or studies, which focus either on purified proteins, and therefore lack cellular complexity, or on cell extracts made from genetically intractable organisms. In order to investigate the ensemble activities of all MAPs on MT dynamics using lysates made from a genetically tractable organism, we developed a cell-free assay for budding yeast lysates using total internal reflection fluorescence (TIRF) microscopy. Lysates were prepared from yeast strains expressing GFP-tubulin. MT polymerization from pre-assembled MT seeds adhered to a coverslip was observed in real time. Through use of cell division cycle () and MT depolymerase mutants, we found that MT polymerization and dynamic instability are dependent on the cell cycle state and the activities of specific MAPs.
微管(MTs)对于细胞结构、货物运输以及有丝分裂过程中染色体和细胞器的分离至关重要。微管的随机生长和收缩,即所谓的动态不稳定性,对于这些功能是必要的。先前确定单个微管相关蛋白(MAPs)如何影响微管动力学的研究,要么通过显微镜观察,提供有限的观察单个微管的机会或操纵条件,要么通过纯化蛋白研究,因此缺乏细胞复杂性,或者通过从遗传上难以处理的生物体提取的细胞提取物进行研究。为了使用来自遗传上可操作的生物体的裂解物来研究所有 MAPs 对微管动力学的整体活性,我们使用全内反射荧光(TIRF)显微镜开发了一种用于芽殖酵母裂解物的无细胞测定法。从表达 GFP-微管蛋白的酵母菌株中制备裂解物。实时观察附着在盖玻片上的预组装微管种子的 MT 聚合。通过使用细胞分裂周期()和 MT 解聚酶突变体,我们发现 MT 聚合和动态不稳定性依赖于细胞周期状态和特定 MAPs 的活性。