Wellcome Trust Centre for Gene Regulation & Expression, College of Life Sciences, University of Dundee, Dundee DD1 5EH, UK.
Dev Cell. 2011 Nov 15;21(5):920-33. doi: 10.1016/j.devcel.2011.09.006.
How kinetochores regulate microtubule dynamics to ensure proper kinetochore-microtubule interactions is unknown. Here, we studied this during early mitosis in Saccharomyces cerevisiae. When a microtubule shrinks and its plus end reaches a kinetochore bound to its lateral surface, the microtubule end attempts to tether the kinetochore. This process often fails and, responding to this failure, microtubule rescue (conversion from shrinkage to growth) occurs, preventing kinetochore detachment from the microtubule end. This rescue is promoted by Stu2 transfer (ortholog of vertebrate XMAP215/ch-TOG) from the kinetochore to the microtubule end. Meanwhile, microtubule rescue distal to the kinetochore is also promoted by Stu2, which is transported by a kinesin-8 motor Kip3 along the microtubule from the kinetochore. Microtubule extension following rescue facilitates interaction with other widely scattered kinetochores, diminishing long delays in collecting the complete set of kinetochores by microtubules. Thus, kinetochore-dependent microtubule rescue ensures efficient and sustained kinetochore-microtubule interactions in early mitosis.
尚不清楚动粒如何调节微管动力学以确保适当的动粒-微管相互作用。在这里,我们在酿酒酵母的早期有丝分裂过程中研究了这一过程。当微管收缩并且其正极到达与侧表面结合的动粒时,微管末端试图将动粒系留。这个过程常常失败,并且为了响应这种失败,微管救援(从收缩转化为生长)发生,防止动粒从微管末端脱离。这种救援是由动粒到微管末端的 Stu2 转移(脊椎动物 XMAP215/ch-TOG 的同源物)促进的。同时,Stu2 也促进了动粒远端的微管救援,它通过驱动蛋白-8 马达 Kip3 沿微管从动粒运输。救援后的微管延伸促进了与其他广泛分散的动粒的相互作用,减少了通过微管收集整套动粒的长时间延迟。因此,动粒依赖性微管救援确保了早期有丝分裂中有效和持续的动粒-微管相互作用。