Department of Molecular Oncology, Institute of Development, Aging and Cancer, Tohoku University, Miyagi 980-8575, Japan.
J Biochem. 2012 Nov;152(5):415-24. doi: 10.1093/jb/mvs109. Epub 2012 Sep 20.
Chromosome segregation is carried out by dynamic interplay between kinetochores and microtubules. First, kinetochores are efficiently captured by microtubules. Then, flexible interactions between kinetochores and microtubules allow proper orientation of chromosomes aligned on the centre of the spindle. Finally, microtubules stably attached to kinetochores drag the chromosomes towards the spindle poles. During these processes, the mode of interaction of kinetochores with microtubules changes from lateral to end-on attachment, accompanied by changes in kinetochore structure/composition and microtubule dynamics. The molecular mechanisms for stable kinetochore-microtubule attachment have been progressively revealed in recent years. On the other hand, the mechanism of dynamic regulation of kinetochore-microtubule interaction in early mitosis, which is crucial for faithful chromosome segregation, continues to be elusive. Here I focus on this early step of chromosome segregation and discuss how kinetochores establish proper attachments to microtubules.
染色体分离是通过动粒和微管之间的动态相互作用来完成的。首先,动粒被微管有效地捕获。然后,动粒和微管之间的灵活相互作用允许在纺锤体中心排列的染色体正确定向。最后,稳定附着在动粒上的微管将染色体拉向纺锤体两极。在这些过程中,动粒与微管的相互作用模式从侧向附着转变为端到端附着,同时动粒结构/组成和微管动力学也发生变化。近年来,稳定的动粒-微管附着的分子机制逐渐被揭示。另一方面,在有丝分裂早期,动粒-微管相互作用的动态调节机制对于确保染色体的正确分离至关重要,但仍不清楚其机制。在这里,我将重点讨论染色体分离的这个早期步骤,并讨论动粒如何与微管建立适当的连接。