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微管成核:超越模板。

Microtubule nucleation: beyond the template.

机构信息

The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.

出版信息

Nat Rev Mol Cell Biol. 2017 Nov;18(11):702-710. doi: 10.1038/nrm.2017.75. Epub 2017 Aug 23.

Abstract

Microtubules are cytoskeletal filaments central to a wide range of essential cellular functions in eukaryotic cells. Consequently, cells need to exert tight control over when, where and how many microtubules are being made. Whereas the regulation of microtubule dynamics is well studied, the molecular mechanisms of microtubule nucleation are still poorly understood. Next to the established master template of nucleation, the γ-tubulin ring complex, other microtubule-associated proteins that affect microtubule dynamic properties have recently been found to contribute to nucleation. It has begun to emerge that the nucleation efficiency is controlled not only by template activity but also by, either additionally or alternatively, the stabilization of the nascent microtubule 'nucleus'. This suggests a simple conceptual framework for the mechanisms regulating microtubule nucleation in cells.

摘要

微管是真核细胞中广泛存在的细胞骨架丝,对多种基本细胞功能至关重要。因此,细胞需要对何时、何地以及制造多少微管进行严格控制。尽管微管动力学的调节已经得到了很好的研究,但微管成核的分子机制仍知之甚少。除了已确立的成核主模板——γ-微管蛋白环复合物外,最近还发现其他影响微管动态特性的微管相关蛋白也有助于成核。人们开始认识到,成核效率不仅受模板活性的控制,而且还受新生微管“核”的稳定作用的控制,这种稳定作用要么是额外的,要么是替代的。这为细胞中调节微管成核的机制提供了一个简单的概念框架。

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