Wellcome Trust Centre for Gene Regulation & Expression, University of Dundee, Dundee DD1 5EH, UK.
Dev Cell. 2010 Feb 16;18(2):248-59. doi: 10.1016/j.devcel.2009.12.018.
In early mitosis, microtubules can be generated at kinetochores as well as at spindle poles. However, the role and regulation of kinetochore-derived microtubules have been unclear. In general, metaphase spindle microtubules are oriented such that their plus ends bind to kinetochores. However, we now have evidence that, during early mitosis in budding yeast, microtubules are generated at kinetochores with distal plus ends. These kinetochore-derived microtubules interact along their length with microtubules that extend from a spindle pole, facilitating kinetochore loading onto the lateral surface of spindle pole microtubules. Once kinetochores are loaded, microtubules are no longer generated at kinetochores, and those that remain disappear rapidly and do not contribute to the metaphase spindle. Stu2 (the ortholog of vertebrate XMAP215/ch-TOG) localizes to kinetochores and plays a central role in regulating kinetochore-derived microtubules. Our work provides insight into microtubule generation at kinetochores and the mechanisms that facilitate initial kinetochore interaction with spindle pole microtubules.
在有丝分裂早期,微管可以在动粒和纺锤体两极生成。然而,动粒衍生微管的作用和调控一直不清楚。一般来说,中期纺锤体微管的取向是其正端与动粒结合。然而,我们现在有证据表明,在芽殖酵母的有丝分裂早期,微管是从动粒上具有远端正端的位置生成的。这些动粒衍生的微管沿着它们的长度与从纺锤体极延伸的微管相互作用,促进动粒加载到纺锤体极微管的侧面。一旦动粒被加载,微管就不再在动粒上生成,并且那些剩余的微管迅速消失,不会对中期纺锤体做出贡献。Stu2(脊椎动物 XMAP215/ch-TOG 的同源物)定位于动粒,在调控动粒衍生微管中发挥核心作用。我们的工作深入了解了动粒处微管的生成以及促进动粒与纺锤体极微管初始相互作用的机制。