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A Bir1p–Sli15p Kinetochore Passenger Complex Regulates Septin Organization during Anaphase

机译:Bir1p–Sli15p线粒体客运大楼在后期调节Septin的组织。

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摘要

Kinetochore–passenger complexes in metazoans have been proposed to coordinate the segregation of chromosomes in anaphase with the induction of cytokinesis. Passenger protein homologues in the budding yeast Saccharomyces cerevisiae play a critical role early in mitosis, ensuring proper biorientation of kinetochore–microtubule attachments. Our recent work has implicated the passenger protein Bir1p (Survivin) and the inner kinetochore complex centromere binding factor 3 (CBF3) in the regulation of septin dynamics during anaphase. Here, we present data that is consistent with there being multiple passenger protein complexes. Our data show that Bir1p links together a large passenger complex containing Ndc10p, Sli15p (INCENP), and Ipl1p (Aurora B) and that the interaction between Bir1p and Sli15p is specifically involved in regulating septin dynamics during anaphase. Neither conditional alleles nor mutants of BIR1 that disrupt the interaction between Bir1p and Sli15p resulted in mono-attached kinetochores, suggesting that the Bir1p–Sli15p complex functions in anaphase and independently from Sli15p–Ipl1p complexes. We present a model for how discrete passenger complexes coordinate distinct aspects of mitosis.
机译:已经提出了后生动物的动线虫-客体复合物可以协调后期染色体的分离与胞质分裂的诱导。发芽的酵母中的客运蛋白同源物在有丝分裂的早期起关键作用,从而确保了动线粒体-微管附件的正确生物取向。我们最近的工作已牵涉到乘客蛋白Bir1p(Survivin)和内部动粒复合体着丝粒结合因子3(CBF3)在后期的隔膜动力学调节中。在这里,我们提出的数据与存在多个客体蛋白复合物是一致的。我们的数据表明Bir1p将包含Ndc10p,Sli15p(INCENP)和Ipl1p(Aurora B)的大型客运复合体链接在一起,并且Bir1p和Sli15p之间的相互作用特别参与后期调控隔膜动力学。有条件的等位基因或BIR1的突变体都不会破坏Bir1p和Sli15p之间的相互作用,不会导致单链动植物,这表明Bir1p–Sli15p复合物在后期发挥功能,并且独立于Sli15p–Ipl1p复合物。我们提出了一个模型,用于离散的客运专区如何协调有丝分裂的各个方面。

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