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由γ-微管蛋白复合体介导的微管成核的调控。

Regulation of microtubule nucleation mediated by γ-tubulin complexes.

作者信息

Sulimenko Vadym, Hájková Zuzana, Klebanovych Anastasiya, Dráber Pavel

机构信息

Department of Biology of Cytoskeleton, Institute of Molecular Genetics, Academy of Sciences of the Czech Republic, Vídeňská 1083, 142 20, Prague 4, Czech Republic.

出版信息

Protoplasma. 2017 May;254(3):1187-1199. doi: 10.1007/s00709-016-1070-z. Epub 2017 Jan 10.

Abstract

The microtubule cytoskeleton is critically important for spatio-temporal organization of eukaryotic cells. The nucleation of new microtubules is typically restricted to microtubule organizing centers (MTOCs) and requires γ-tubulin that assembles into multisubunit complexes of various sizes. γ-Tubulin ring complexes (TuRCs) are efficient microtubule nucleators and are associated with large number of targeting, activating and modulating proteins. γ-Tubulin-dependent nucleation of microtubules occurs both from canonical MTOCs, such as spindle pole bodies and centrosomes, and additional sites such as Golgi apparatus, nuclear envelope, plasma membrane-associated sites, chromatin and surface of pre-existing microtubules. Despite many advances in structure of γ-tubulin complexes and characterization of γTuRC interacting factors, regulatory mechanisms of microtubule nucleation are not fully understood. Here, we review recent work on the factors and regulatory mechanisms that are involved in centrosomal and non-centrosomal microtubule nucleation.

摘要

微管细胞骨架对于真核细胞的时空组织至关重要。新微管的成核通常局限于微管组织中心(MTOC),并且需要γ-微管蛋白组装成各种大小的多亚基复合物。γ-微管蛋白环复合物(TuRC)是高效的微管成核剂,并与大量靶向、激活和调节蛋白相关联。微管的γ-微管蛋白依赖性成核既发生在典型的MTOC,如纺锤体极体和中心体,也发生在其他位点,如高尔基体、核膜、质膜相关位点、染色质和现有微管的表面。尽管在γ-微管蛋白复合物的结构和γTuRC相互作用因子的表征方面取得了许多进展,但微管成核的调控机制仍未完全了解。在这里,我们综述了关于参与中心体和非中心体微管成核的因子和调控机制的最新研究工作。

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