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首页> 外文期刊>Journal of cell biology >Aurora B controls kinetochore–microtubule attachments by inhibiting Ska complex–KMN network interaction
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Aurora B controls kinetochore–microtubule attachments by inhibiting Ska complex–KMN network interaction

机译:Aurora B通过抑制Ska复杂分子-KMN网络相互作用来控制线粒体-微管附件

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The KMN network (named according to the acronym for KNL1, Mis12, and Ndc80) and the more recently identified Ska complex (Ska1–3) have been shown to mediate kinetochore (KT)–microtubule (MT) attachments. How these two complexes cooperate to achieve stable end-on attachments remains unknown. In this paper, we show that Aurora B negatively regulates the localization of the Ska complex to KTs and that recruitment of the Ska complex to KTs depends on the KMN network. We identified interactions between members of the KMN and Ska complexes and demonstrated that these interactions are regulated by Aurora B. Aurora B directly phosphorylated Ska1 and Ska3 in vitro, and expression of phosphomimetic mutants of Ska1 and Ska3 impaired Ska KT recruitment and formation of stable KT–MT fibers (K-fibers), disrupting mitotic progression. We propose that Aurora B phosphorylation antagonizes the interaction between the Ska complex and the KMN network, thereby controlling Ska recruitment to KTs and stabilization of KT–MT attachments.
机译:KMN网络(根据KNL1,Mis12和Ndc80的首字母缩写命名)和最近发现的Ska复合体(Ska1-3)已显示出介导动粒(KT)-微管(MT)附件。这两个复合体如何协作以实现稳定的末端附着仍然未知。在本文中,我们表明Aurora B对Ska复合体到KT的定位有负面影响,而Ska复合体到KT的募集取决于KMN网络。我们确定了KMN和Ska复合体成员之间的相互作用,并证明了这些相互作用受Aurora B的调节。AuroraB在体外直接磷酸化Ska1和Ska3,Ska1和Ska3的磷酸化突变体的表达削弱了Ska KT募集和稳定KT的形成。 –MT纤维(K纤维),破坏有丝分裂进程。我们建议Aurora B磷酸化拮抗Ska复合物和KMN网络之间的相互作用,从而控制Ska向KT的募集和KT-MT附件的稳定。

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