Cimini Daniela
Department of Biological Sciences, Virginia Polytechnic Institute and State University, Blacksburg, Virginia 24061, USA.
Cell Cycle. 2007 Jul 1;6(13):1558-64. doi: 10.4161/cc.6.13.4452. Epub 2007 May 18.
Merotelic kinetochore orientation is a kinetochore-microtubule mis-attachment in which a single kinetochore binds microtubules to both spindle poles, rather than just one. Merotelic attachments occur frequently in early mitosis and can induce anaphase lagging chromosomes and aneuploidy if not corrected before anaphase onset. Merotelic kinetochore orientation does not interfere with chromosome alignment at the metaphase plate and does not activate the mitotic spindle checkpoint. However, a correction mechanism for merotelic attachment reduces the number of merotelic kinetochores entering anaphase, thus preventing chromosome mis-segregation. Results from many different studies support the idea that Aurora B kinase plays a critical role in this merotelic correction mechanism by phosphorylating key substrates at the kinetochore and promoting turnover of kinetochore microtubules. In addition, recent studies are starting to identify the possible 'sensors' of the system that would be able to detect the mis-attachment and communicate this to Aurora B. Here, I review these studies and discuss a model for how merotelic kinetochore orientation could be detected and corrected before anaphase onset.
错向动粒定向是一种动粒-微管错误附着,即单个动粒与来自纺锤体两极的微管结合,而不是仅与一极的微管结合。错向附着在有丝分裂早期频繁发生,如果在后期开始前未得到纠正,可导致后期滞后染色体和非整倍体。错向动粒定向并不干扰染色体在中期板上的排列,也不会激活有丝分裂纺锤体检查点。然而,一种针对错向附着的纠正机制可减少进入后期的错向动粒数量,从而防止染色体错误分离。许多不同研究的结果支持这样一种观点,即极光激酶B通过磷酸化动粒上的关键底物并促进动粒微管的周转,在这种错向纠正机制中发挥关键作用。此外,最近的研究开始确定该系统可能的“传感器”,这些传感器能够检测到错误附着并将此信息传递给极光激酶B。在此,我综述这些研究,并讨论一个关于在后期开始前如何检测和纠正错向动粒定向的模型。