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Cytokinesis and Midzone Microtubule Organization in Caenorhabditis elegans Require the Kinesin-like Protein ZEN-4

机译:秀丽隐杆线虫的胞质分裂和中区微管组织需要驱动蛋白样蛋白ZEN-4。

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摘要

Members of the MKLP1 subfamily of kinesin motor proteins localize to the equatorial region of the spindle midzone and are capable of bundling antiparallel microtubules in vitro. Despite these intriguing characteristics, it is unclear what role these kinesins play in dividing cells, particularly within the context of a developing embryo. Here, we report the identification of a null allele of zen-4, an MKLP1 homologue in the nematode Caenorhabditis elegans, and demonstrate that ZEN-4 is essential for cytokinesis. Embryos deprived of ZEN-4 form multinucleate single-celled embryos as they continue to cycle through mitosis but fail to complete cell division. Initiation of the cytokinetic furrow occurs at the normal time and place, but furrow propagation halts prematurely. Time-lapse recordings and microtubule staining reveal that the cytokinesis defect is preceded by the dissociation of the midzone microtubules. We show that ZEN-4 protein localizes to the spindle midzone during anaphase and persists at the midbody region throughout cytokinesis. We propose that ZEN-4 directly cross-links the midzone microtubules and suggest that these microtubules are required for the completion of cytokinesis.
机译:驱动蛋白运动蛋白的MKLP1亚家族的成员位于纺锤体中区的赤道区域,并能够在体外捆绑反平行微管。尽管有这些吸引人的特征,但尚不清楚这些驱动蛋白在分裂细胞中起什么作用,特别是在发育中的胚胎中。在这里,我们报告的线虫Caenorhabditis elegans的MKLP1同源基因zen-4的无效等位基因的鉴定,并证明ZEN-4对于胞质分裂是必不可少的。被剥夺ZEN-4的胚胎会形成多核单细胞胚胎,因为它们继续在有丝分裂中循环,但无法完成细胞分裂。细胞动力学犁沟的发生在正常的时间和地点,但是犁沟的繁殖过早地停止了。延时记录和微管染色显示,胞质分裂缺陷是由中区微管解离所致。我们显示ZEN-4蛋白在后期定位于纺锤体中区,并在整个胞质分裂过程中持续存在于中体区域。我们建议Z​​EN-4直接交联中区微管,并建议这些微管是完成胞质分裂所必需的。

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