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Length-dependent anisotropic scaling of spindle shape

机译:主轴形状的长度依赖性各向异性缩放

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Spindle length varies dramatically across species and during early development to segregate chromosomes optimally. Both intrinsic factors, such as regulatory molecules, and extrinsic factors, such as cytoplasmic volume, determine spindle length scaling. However, the properties that govern spindle shape and whether these features can be modulated remain unknown. Here, we analyzed quantitatively how the molecular players which regulate microtubule dynamics control the kinetics of spindle formation and shape. We find that, in absence of Clasp1 and Clasp2, spindle assembly is biphasic due to unopposed inward pulling forces from the kinetochore-fibers and that kinetochore-fibers also alter spindle geometry. We demonstrate that spindle shape scaling is independent of the nature of the molecules that regulate dynamic microtubule properties, but is dependent on the steady-state metaphase spindle length. The shape of the spindle scales anisotropically with increasing length. Our results suggest that intrinsic mechanisms control the shape of the spindle to ensure the efficient capture and alignment of chromosomes independently of spindle length.
机译:纺锤体长度在不同物种之间以及在早期发育过程中差异很大,以最佳地隔离染色体。内在因素(例如调节分子)和外在因素(例如细胞质体积)都决定纺锤体的长度缩放。但是,控制主轴形状以及是否可以调制这些特征的属性仍然未知。在这里,我们定量分析了调节微管动力学的分子参与者如何控制纺锤形成和形状的动力学。我们发现,在没有Clasp1和Clasp2的情况下,主轴组件是双相的,这是由于来自动线粒纤维的无向内的拉力,并且动线粒纤维也改变了主轴的几何形状。我们证明纺锤形状缩放独立于调节动态微管属性的分子的性质,但取决于稳态中期纺锤体的长度。主轴的形状随着长度的增加而各向异性地缩放。我们的结果表明,内在机制控制纺锤的形状,以确保独立于纺锤长度而有效捕获和对齐染色体。

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