Division of Molecular Biology, Laboratory of Cell Biophysics, Ruđer Bošković Institute, Bijenička cesta 54, Zagreb 10000, Croatia.
Department of Electronics, Microelectronics, Computer and Intelligent Systems, Faculty of Electrical Engineering and Computing, University of Zagreb, Unska 3, Zagreb 10000, Croatia.
Curr Biol. 2022 Jun 6;32(11):2480-2493.e6. doi: 10.1016/j.cub.2022.04.035. Epub 2022 May 9.
Forces produced by motor proteins and microtubule dynamics within the mitotic spindle are crucial for proper chromosome segregation. In addition to linear forces, rotational forces or torques are present in the spindle, which are reflected in the left-handed twisted shapes of microtubule bundles that make the spindle chiral. However, the biological role and molecular origins of spindle chirality are unknown. By developing methods for measuring the spindle twist, we show that spindles are most chiral near the metaphase-to-anaphase transition. To assess the role of chirality in spindle mechanics, we compressed the spindles along their axis. This resulted in a stronger left-handed twist, suggesting that the twisted shape allows for a mechanical response to forces. Inhibition or depletion of motor proteins that perform chiral stepping, Eg5/kinesin-5, Kif18A/kinesin-8, MKLP1/kinesin-6, and dynein, decreased the left-handed twist or led to right-handed twist, implying that these motors regulate the twist by rotating microtubules within their antiparallel overlaps or at the spindle pole. A right-handed twist was also observed after the depletion of the microtubule nucleator augmin, indicating its contribution to the twist through the nucleation of antiparallel bridging microtubules. The uncovered switch from left-handed to right-handed twist reveals the existence of competing mechanisms that promote twisting in opposite directions. As round spindles are more twisted than the elongated ones are, we infer that bending and twisting moments are generated by similar molecular mechanisms and propose a physiological role for spindle chirality in allowing the spindle to absorb mechanical load. VIDEO ABSTRACT.
马达蛋白产生的力和有丝分裂纺锤体中的微管动力学对于正确的染色体分离至关重要。除了线性力之外,纺锤体中还存在旋转力或扭矩,这反映在使纺锤体手性的微管束的左旋扭曲形状中。然而,纺锤体手性的生物学作用和分子起源尚不清楚。通过开发测量纺锤体扭曲的方法,我们发现纺锤体在中期到后期过渡附近最具手性。为了评估手性在纺锤体力学中的作用,我们沿着纺锤体的轴压缩纺锤体。这导致了更强的左旋扭曲,表明扭曲的形状允许对力产生机械响应。抑制或耗尽执行手性步进的马达蛋白,Eg5/驱动蛋白-5、Kif18A/驱动蛋白-8、MKLP1/驱动蛋白-6 和动力蛋白,会降低左旋扭曲或导致右旋扭曲,这表明这些马达蛋白通过旋转它们的平行重叠内或在纺锤体极处的微管来调节扭曲。在微管核形成因子 augmin 耗尽后也观察到右旋扭曲,表明其通过形成平行桥接微管对手性的贡献。从左旋到右旋扭曲的这种转变揭示了存在促进相反方向扭曲的竞争机制。由于圆形纺锤体比伸长纺锤体更扭曲,我们推断弯曲和扭曲力矩是由类似的分子机制产生的,并提出了纺锤体手性在允许纺锤体吸收机械负荷方面的生理作用。视频摘要。