Suppr超能文献

纺锤体中微管壁上的 Augmin 依赖性微管核形成。

Augmin-dependent microtubule nucleation at microtubule walls in the spindle.

机构信息

Division of Biological Science, Graduate School of Science, Nagoya University, Chikusa, Nagoya 464-8602, Japan.

出版信息

J Cell Biol. 2013 Jul 8;202(1):25-33. doi: 10.1083/jcb.201304031. Epub 2013 Jul 1.

Abstract

The formation of a functional spindle requires microtubule (MT) nucleation from within the spindle, which depends on augmin. How augmin contributes to MT formation and organization is not known because augmin-dependent MTs have never been specifically visualized. In this paper, we identify augmin-dependent MTs and their connections to other MTs by electron tomography and 3D modeling. In metaphase spindles of human cells, the minus ends of MTs were located both around the centriole and in the body of the spindle. When augmin was knocked down, the latter population of MTs was significantly reduced. In control cells, we identified connections between the wall of one MT and the minus end of a neighboring MT. Interestingly, the connected MTs were nearly parallel, unlike other examples of end-wall connections between cytoskeletal polymers. Our observations support the concept of augmin-dependent MT nucleation at the walls of existing spindle MTs. Furthermore, they suggest a mechanism for maintaining polarized MT organization, even when noncentrosomal MT initiation is widespread.

摘要

功能性纺锤体的形成需要纺锤体内微管(MT)的核形成,这取决于微管相关蛋白复合物。然而,微管相关蛋白复合物如何促进 MT 的形成和组织尚不清楚,因为从未专门观察到微管相关蛋白复合物依赖性 MT。在本文中,我们通过电子断层扫描和 3D 建模来鉴定微管相关蛋白复合物依赖性 MT 及其与其他 MT 的连接。在人类细胞的中期纺锤体中,MT 的负端既位于中心粒周围,也位于纺锤体的主体中。当微管相关蛋白复合物被敲低时,后者的 MT 群体明显减少。在对照细胞中,我们鉴定了一个 MT 的壁与相邻 MT 的负端之间的连接。有趣的是,连接的 MT 几乎是平行的,与细胞骨架聚合物之间其他末端壁连接的例子不同。我们的观察结果支持在现有纺锤体 MT 的壁上进行微管相关蛋白复合物依赖性 MT 核形成的概念。此外,它们还提出了一种即使非中心体 MT 起始广泛存在也能维持极化 MT 组织的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3c6/3704994/6193a0be765b/JCB_201304031_Fig1.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验