Haase Julian, Bonner Mary Kate, Halas Hyunmi, Kelly Alexander E
Laboratory of Biochemistry & Molecular Biology, National Cancer Institute, NIH, Bethesda, MD 20892, USA.
Laboratory of Biochemistry & Molecular Biology, National Cancer Institute, NIH, Bethesda, MD 20892, USA.
Dev Cell. 2017 Sep 25;42(6):640-654.e5. doi: 10.1016/j.devcel.2017.08.022.
The chromosomal passenger complex (CPC) localizes to centromeres in early mitosis to activate its subunit Aurora B kinase. However, it is unclear whether centromeric CPC localization contributes to CPC functions beyond Aurora B activation. Here, we show that an activated CPC that cannot localize to centromeres supports functional assembly of the outer kinetochore but is unable to correct errors in kinetochore-microtubule attachment in Xenopus egg extracts. We find that CPC has two distinct roles at centromeres: one to selectively phosphorylate Ndc80 to regulate attachment and a second, conserved kinase-independent role in the proper composition of inner kinetochore proteins. Although a fully assembled inner kinetochore is not required for outer kinetochore assembly, we find it is essential to recruit tension indicators, such as BubR1 and 3F3/2, to erroneous attachments. We conclude centromeric CPC is necessary for tension-dependent removal of erroneous attachments and for the kinetochore composition required to detect tension loss.
染色体乘客复合体(CPC)在有丝分裂早期定位于着丝粒,以激活其亚基极光激酶B(Aurora B kinase)。然而,尚不清楚着丝粒处的CPC定位是否有助于CPC在激活Aurora B之外的功能。在此,我们表明,无法定位于着丝粒的激活型CPC支持外着丝粒的功能组装,但无法纠正非洲爪蟾卵提取物中着丝粒-微管附着的错误。我们发现CPC在着丝粒处有两个不同的作用:一个是选择性磷酸化Ndc80以调节附着,另一个是在内着丝粒蛋白的正确组成中起保守的非激酶依赖性作用。虽然外着丝粒组装不需要完全组装好的内着丝粒,但我们发现,将诸如BubR1和3F3/2等张力指示剂募集到错误附着处至关重要。我们得出结论,着丝粒CPC对于依赖张力去除错误附着以及检测张力丧失所需的着丝粒组成是必需的。