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End-on microtubule-dynein interactions and pulling-based positioning of microtubule organizing centers

机译:末端微管-动力蛋白相互作用和微管组织中心的基于拉动的定位

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摘要

During important cellular processes such as centrosome and spindle positioning, dynein at the cortex interacts with dynamic microtubules in an apparent "end-on" fashion. It is well-established that dynein can generate forces by moving laterally along the microtubule lattice, but much less is known about dynein's interaction with dynamic microtubule ends. In this paper, we review recent in vitro experiments that show that dynein, attached to an artifcial cortex, is able to capture microtubule ends, regulate microtubule dynamics and mediate the generation of pulling forces on shrinking microtu-bules. We further review existing ideas on the involvement of dynein-mediated cortical pulling forces in the positioning of microtubule organizing centers such as centrosomes. Recent in vitro experiments have demonstrated that cortical pulling forces in combination with pushing forces can lead to reliable centering of microtubule asters in quasi two-dimensional microfabricated chambers. In these experiments, pushing leads to slipping of microtubule ends along the chamber boundaries, resulting in an anisotropic distribution of cortical microtubule contacts that favors centering, once pulling force generators become engaged. This effect is predicted to be strongly geometry-dependent, and we therefore fnally discuss ongoing efforts to repeat these experiments in three-dimensional, spherical and deformable geometries.
机译:在重要的细胞过程中,如中心体和纺锤体定位中,皮层中的达因以明显的“端对端”方式与动态微管相互作用。公认的是,动力蛋白可以通过沿微管晶格横向移动而产生力,但对于动力蛋白与动态微管末端的相互作用知之甚少。在本文中,我们回顾了最近的体外实验,结果表明,附着在人造皮层上的达因可以捕获微管末端,调节微管动力学,并介导收缩的微管上拉力的产生。我们进一步审查有关动力蛋白介导的皮层拉力参与微管组织中心如中心体的定位的现有想法。最近的体外实验表明,皮层的拉力与推力相结合可导致微管翠菊在准二维微加工腔室内可靠居中。在这些实验中,推动会导致微管末端沿着腔室边界滑动,一旦牵拉力产生器接合,就会导致皮质微管接触的各向异性分布,有利于定心。预计这种效果与几何形状密切相关,因此我们最后讨论了在三维,球形和可变形几何形状中重复这些实验的持续努力。

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