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Dynein–Dynactin–NuMA clusters generate cortical spindle-pulling forces as a multi-arm ensemble

机译:Dynein–Dynactin–NuMA簇产生多臂合奏的皮层纺锤体牵引力

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摘要

To position the mitotic spindle within the cell, dynamic plus ends of astral microtubules are pulled by membrane-associated cortical force-generating machinery. However, in contrast to the chromosome-bound kinetochore structure, how the diffusion-prone cortical machinery is organized to generate large spindle-pulling forces remains poorly understood. Here, we develop a light-induced reconstitution system in human cells. We find that induced cortical targeting of NuMA, but not dynein, is sufficient for spindle pulling. This spindle-pulling activity requires dynein-dynactin recruitment by NuMA’s N-terminal long arm, dynein-based astral microtubule gliding, and NuMA’s direct microtubule-binding activities. Importantly, we demonstrate that cortical NuMA assembles specialized focal structures that cluster multiple force-generating modules to generate cooperative spindle-pulling forces. This clustering activity of NuMA is required for spindle positioning, but not for spindle-pole focusing. We propose that cortical Dynein-Dynactin-NuMA (DDN) clusters act as the core force-generating machinery that organizes a multi-arm ensemble reminiscent of the kinetochore.
机译:为了将有丝分裂纺锤体定位在细胞内,利用膜相关的皮层力产生机制拉动星形微管的动态末端。然而,与染色体结合的线粒体结构相反,易于扩散的皮层机械如何组织以产生大的纺锤体拉力仍然知之甚少。在这里,我们开发了人类细胞中的光诱导重建系统。我们发现诱导皮层靶向的NuMA,但不是达因宁,足以纺锤体。这种纺锤体活动需要通过NuMA的N端长臂,基于动力蛋白的星状微管滑动来招募动力蛋白-动力蛋白,以及NuMA的直接微管结合活性。重要的是,我们证明了皮质NuMA组装了专门的聚焦结构,该聚焦结构将多个力生成模块聚集在一起以产生协作的主轴牵引力。 NuMA的这种聚类活动对于主轴定位是必需的,但对于主轴-极聚焦则不是必需的。我们建议皮质Dynein-Dynactin-NuMA(DDN)群集充当组织多臂合奏,使人联想起动粒的核心力产生机器。

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