Institute for Research in Biomedicine (IRB Barcelona), C/ Baldiri Reixac 10, Barcelona, Spain.
Institute for Research in Biomedicine (IRB Barcelona), C/ Baldiri Reixac 10, Barcelona, Spain.
Curr Biol. 2015 Mar 30;25(7):R294-9. doi: 10.1016/j.cub.2015.02.006.
Microtubules mediate important cellular processes by forming highly ordered arrays. Organization of these networks is achieved by nucleating and anchoring microtubules at centrosomes and other structures collectively known as microtubule-organizing centers (MTOCs). However, the diverse microtubule configurations found in different cell types may not be generated and maintained by MTOCs alone. Work over the last few years has revealed a mechanism that has the capacity to generate cell-type-specific microtubule arrays independently of a specific organizer: nucleation of microtubules from the lateral surface of pre-existing microtubules. This type of nucleation requires cooperation between two different multi-subunit protein complexes, augmin and the γ-tubulin ring complex (γTuRC). Here we review recent molecular insight into microtubule-dependent nucleation and discuss the possibility that the augmin-γTuRC module, initially described in mitosis, may broadly contribute to microtubule organization also in non-mitotic cells.
微管通过形成高度有序的阵列来介导重要的细胞过程。这些网络的组织是通过在中心体和其他被称为微管组织中心 (MTOC) 的结构处起始和锚定微管来实现的。然而,不同细胞类型中发现的不同微管构型可能不仅仅是由 MTOC 产生和维持的。过去几年的工作揭示了一种能够独立于特定组织者产生细胞类型特异性微管阵列的机制:从预先存在的微管的侧面起始微管的核化。这种核化需要两种不同的多亚基蛋白复合物——augmin 和 γ-微管蛋白环复合物 (γTuRC) 之间的合作。在这里,我们回顾了最近关于微管依赖性核化的分子见解,并讨论了 augmin-γTuRC 模块最初在有丝分裂中描述的可能性,该模块可能广泛有助于非有丝分裂细胞中的微管组织。