Department of Biology, University of Pennsylvania, Philadelphia, PA 19104, USA.
Trends Cell Biol. 2011 Mar;21(3):133-40. doi: 10.1016/j.tcb.2010.10.007. Epub 2010 Nov 22.
Maintaining genome integrity during cell division requires regulated interactions between chromosomes and spindle microtubules. To ensure that daughter cells inherit the correct chromosomes, the sister kinetochores must attach to opposite spindle poles. Tension across the centromere stabilizes correct attachments, whereas phosphorylation of kinetochore substrates by the conserved Ipl1/Aurora B kinase selectively eliminates incorrect attachments. Here, we review our current understanding of how mechanical forces acting on the kinetochore are linked to biochemical changes to control chromosome segregation. We discuss models for tension sensing and regulation of kinetochore function downstream of Aurora B, and mechanisms that specify Aurora B localization to the inner centromere and determine its interactions with substrates at distinct locations.
在细胞分裂过程中维持基因组完整性需要染色体和纺锤体微管之间的调控相互作用。为了确保子细胞遗传正确的染色体,姐妹动粒必须附着在纺锤体的相反两极。着丝粒上的张力稳定正确的连接,而保守的 Ipl1/Aurora B 激酶对动粒底物的磷酸化则选择性地消除不正确的连接。在这里,我们回顾了我们目前对作用在动粒上的机械力如何与生化变化联系起来以控制染色体分离的理解。我们讨论了张力感应模型和 Aurora B 下游动粒功能的调节,以及指定 Aurora B 定位到着丝粒内部并确定其与不同位置底物相互作用的机制。