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How the kinetochore couples microtubule force and centromere stretch to move chromosomes

机译:线粒体如何结合微管力和着丝粒拉伸以移动染色体

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摘要

The Ndc80 complex (Ndc80, Nuf2, Spc24 and Spc25) is a highly conserved kinetochore protein essential for end-on anchorage to spindle microtubule plus ends and for force generation coupled to plus-end polymerization and depolymerization. Spc24/Spc25 at one end of the Ndc80 complex binds the kinetochore. The N-terminal tail and CH domains of Ndc80 bind microtubules, and an internal domain binds microtubule-associated proteins (MAPs) such as the Dam1 complex. To determine how the microtubule-and MAP-binding domains of Ndc80 contribute to force production at the kinetochore in budding yeast, we have inserted a FRET tension sensor into the Ndc80 protein about halfway between its microtubule-binding and internal loop domains. The data support a mechanical model of force generation at metaphase where the position of the kinetochore relative to the microtubule plus end reflects the relative strengths of microtubule depolymerization, centromere stretch and microtubule-binding interactions with the Ndc80 and Dam1 complexes.
机译:Ndc80复合物(Ndc80,Nuf2,Spc24和Spc25)是高度保守的动粒蛋白质,对于将末端固定在纺锤微管正末端上以及与正末端聚合和解聚反应产生的力至关重要。 Ndc80复合体一端的Spc24 / Spc25结合了线粒体。 Ndc80的N末端尾部和CH结构域结合微管,而内部结构域则结合微管相关蛋白(MAP),例如Dam1复合物。为了确定Ndc80的微管和MAP结合结构域如何促进发芽酵母中线粒体的力产生,我们将FRET张力传感器插入Ndc80蛋白质的微管结合和内部环结构域之间的中间位置。数据支持在中期产生力的力学模型,其中动粒相对于微管正端的位置反映了微管解聚,着丝粒拉伸和与Ndc80和Dam1配合物的微管结合相互作用的相对强度。

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