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Two populations of cytoplasmic dynein contribute to spindle positioning in C. elegans embryos

机译:胞质动力蛋白的两个种群有助于秀丽隐杆线虫胚胎中的纺锤体定位

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The position of the mitotic spindle is tightly controlled in animal cells as it determines the plane and orientation of cell division. Contacts between cytoplasmic dynein and astral microtubules (MTs) at the cell cortex generate pulling forces that position the spindle. An evolutionarily conserved Gα-GPR-1/2~(Pins/LGN)–LIN-5~(Mud/NuMA) cortical complex interacts with dynein and is required for pulling force generation, but the dynamics of this process remain unclear. In this study, by fluorescently labeling endogenous proteins in Caenorhabditis elegans embryos, we show that dynein exists in two distinct cortical populations. One population directly depends on LIN-5, whereas the other is concentrated at MT plus ends and depends on end-binding (EB) proteins. Knockout mutants lacking all EBs are viable and fertile and display normal pulling forces and spindle positioning. However, EB protein–dependent dynein plus end tracking was found to contribute to force generation in embryos with a partially perturbed dynein function, indicating the existence of two mechanisms that together create a highly robust force-generating system.
机译:有丝分裂纺锤体的位置在动物细胞中受到严格控制,因为它决定了细胞分裂的平面和方向。细胞质动力蛋白与细胞皮层的星状微管(MT)之间的接触会产生拉力,从而将纺锤定位。进化上保守的Gα-GPR-1/ 2〜(Pins / LGN)–LIN-5〜(Mud / NuMA)皮质复合物与达因相互作用,是产生拉力的必要条件,但这一过程的动力学尚不清楚。在这项研究中,通过荧光标记秀丽隐杆线虫胚胎中的内源蛋白,我们显示了动力蛋白存在于两个不同的皮质种群中。一个种群直接依赖于LIN-5,而另一个种群则集中在MT加末端,并依赖于末端结合(EB)蛋白。缺乏所有EB的敲除突变体是可行的和肥沃的,并显示出正常的拉力和纺锤体定位。但是,发现依赖EB蛋白的动力蛋白加上末端追踪有助于部分动力蛋白功能受到扰动的胚胎中的力生成,表明存在两种机制共同构成了高度强大的力生成系统。

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