Department of Plant Biology, University of California, Davis, CA, 95616, USA.
New Phytol. 2019 Jun;222(4):1705-1718. doi: 10.1111/nph.15705. Epub 2019 Feb 25.
Contents Summary I. Introduction II. MT arrays in plant cells III. γ-Tubulin and MT nucleation IV. MT nucleation sites or flexible MTOCs in plant cells V. MT-dependent MT nucleation VI. Generating new MTs for spindle assembly VII. Generation of MTs for phragmoplast expansion during cytokinesis VIII. MT generation for the cortical MT array IX. MT nucleation: looking forward Acknowledgements References SUMMARY: Cytoskeletal microtubules (MTs) have a multitude of functions including intracellular distribution of molecules and organelles, cell morphogenesis, as well as segregation of the genetic material and separation of the cytoplasm during cell division among eukaryotic organisms. In response to internal and external cues, eukaryotic cells remodel their MT network in a regulated manner in order to assemble physiologically important arrays for cell growth, cell proliferation, or for cells to cope with biotic or abiotic stresses. Nucleation of new MTs is a critical step for MT remodeling. Although many key factors contributing to MT nucleation and organization are well conserved in different kingdoms, the centrosome, representing the most prominent microtubule organizing centers (MTOCs), disappeared during plant evolution as angiosperms lack the structure. Instead, flexible MTOCs may emerge on the plasma membrane, the nuclear envelope, and even organelles depending on types of cells and organisms and/or physiological conditions. MT-dependent MT nucleation is particularly noticeable in plant cells because it accounts for the primary source of MT generation for assembling spindle, phragmoplast, and cortical arrays when the γ-tubulin ring complex is anchored and activated by the augmin complex. It is intriguing what proteins are associated with plant-specific MTOCs and how plant cells activate or inactivate MT nucleation activities in spatiotemporally regulated manners.
内容概述 I. 引言 II. 植物细胞中的微管三聚体 III. γ-微管蛋白和微管成核 IV. 植物细胞中的微管成核位点或灵活的微管组织中心 V. 依赖微管的微管成核 VI. 为纺锤体组装生成新的微管 VII. 在胞质分裂过程中为形成胞质板生成微管 VIII. 为皮质微管阵列生成微管 IX. 微管成核:展望 Acknowledgements 参考文献 摘要:真核生物细胞中的细胞骨架微管(MTs)具有多种功能,包括分子和细胞器的细胞内分布、细胞形态发生、以及遗传物质的分离和细胞质的分裂。为了组装对细胞生长、细胞增殖或细胞应对生物或非生物胁迫具有生理重要性的阵列,真核细胞会以一种受调控的方式重塑其 MT 网络。新的 MT 的成核是 MT 重塑的关键步骤。尽管许多参与 MT 成核和组织的关键因素在不同的生物界中都得到了很好的保守,但作为最突出的微管组织中心(MTOCs)的中心体,在被子植物的进化过程中消失了。相反,灵活的 MTOCs 可能出现在质膜、核膜甚至细胞器上,这取决于细胞和生物体的类型和/或生理条件。在植物细胞中,依赖微管的微管成核特别明显,因为当 γ-微管蛋白环复合物被 augmin 复合物锚定和激活时,它占组装纺锤体、胞质板和皮质阵列的 MT 生成的主要来源。有趣的是,哪些蛋白质与植物特异性 MTOCs 相关,以及植物细胞如何以时空调节的方式激活或失活 MT 成核活性。