Institute of Biochemistry, ETH Zurich, Schafmattstrasse 18, CH-8093 Zurich, Switzerland.
Eur J Cell Biol. 2012 Feb;91(2):103-6. doi: 10.1016/j.ejcb.2011.10.002. Epub 2011 Nov 21.
The multiple functions of kinetochores are reflected in their complex composition, with over a hundred different proteins, which self-associate in several functional subcomplexes. Most of these kinetochore proteins were identified over the last 10-12 years using a combination of genetic, cell biological, biochemical, and bioinformatic approaches in various model organisms. The key challenge since then has been to determine the structural architecture of kinetochores, define the functions of its different subcomponents, and understand its regulation, both in response to the rapid changes in microtubule dynamics or to sense erroneous attachments for spindle checkpoint signalling. Here, we present some of the key advances obtained in the last six years on the biology of kinetochores, both through our work and through the work of many other groups studying this exciting structure.
动粒的多种功能反映在其复杂的组成上,其中包含一百多种不同的蛋白质,这些蛋白质在几个功能亚基中自我组装。在过去的 10-12 年中,大多数这些动粒蛋白都是通过遗传、细胞生物学、生物化学和生物信息学方法在各种模式生物中结合使用来鉴定的。此后的主要挑战一直是确定动粒的结构架构,定义其不同亚基的功能,并理解其调节,包括对微管动力学快速变化的响应,或感知纺锤体检查点信号的错误附着。在这里,我们介绍了过去六年中在动粒生物学方面取得的一些重要进展,包括我们自己的工作和许多其他研究这一令人兴奋结构的小组的工作。