首页> 外文期刊>Journal of cell biology >Prometaphase spindle maintenance by an antagonistic motor-dependent force balance made robust by a disassembling lamin-B envelope
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Prometaphase spindle maintenance by an antagonistic motor-dependent force balance made robust by a disassembling lamin-B envelope

机译:通过拆解lamin-B外壳使对抗性的与电机有关的力平衡达到前阶段主轴维护的目的

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摘要

We tested the classical hypothesis that astral, prometaphase bipolar mitotic spindles are maintained by balanced outward and inward forces exerted on spindle poles by kinesin-5 and -14 using modeling of in vitro and in vivo data from Drosophila melanogaster embryos. Throughout prometaphase, puncta of both motors aligned on interpolar microtubules (MTs [ipMTs]), and motor perturbation changed spindle length, as predicted. Competitive motility of purified kinesin-5 and -14 was well described by a stochastic, opposing power stroke model incorporating motor kinetics and load-dependent detachment. Motor parameters from this model were applied to a new stochastic force-balance model for prometaphase spindles, providing a good fit to data from embryos. Maintenance of virtual spindles required dynamic ipMTs and a narrow range of kinesin-5 to kinesin-14 ratios matching that found in embryos. Functional perturbation and modeling suggest that this range can be extended significantly by a disassembling lamin-B envelope that surrounds the prometaphase spindle and augments the finely tuned, antagonistic kinesin force balance to maintain robust prometaphase spindles as MTs assemble and chromosomes are pushed to the equator.
机译:我们测试了经典的假设,即使用果蝇黑色素瘤胚胎的体外和体内数据建模,通过驱动蛋白5和-14施加在纺锤极上的平衡的向外和向内的力来维持星体,前中期双极有丝分裂纺锤体。在整个前中期,两个电机的点均对准极间微管(MT [ipMTs]),并且电机扰动改变了主轴长度,如预期的那样。纯化的驱动蛋白5和-14的竞争运动性很好地描述了一种随机的,对立的动力冲程模型,该模型结合了运动动力学和负荷依赖性脱离。该模型的运动参数被应用于前中期纺锤体的新的随机力平衡模型,非常适合胚胎数据。维持虚拟纺锤体需要动态ipMT,并且需要在胚胎中发现的较窄范围的kinesin-5与kinesin-14比例匹配。功能性扰动和建模表明,可通过拆解围绕前中期纺锤体的lamin-B包膜显着扩展该范围,并在MT组装并将染色体推向赤道时增强微调的拮抗驱动蛋白平衡,以维持坚固的前中期纺锤体。

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