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Kinesin-like Protein CHO1 Is Required for the Formation of Midbody Matrix and the Completion of Cytokinesis in Mammalian Cells

机译:肌动蛋白样蛋白CHO1是哺乳动物细胞中体基质的形成和胞质分裂完成所必需的。

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CHO1 is a mammalian kinesin-like motor protein of the MKLP1 subfamily. It associates with the spindle midzone during anaphase and concentrates to a midbody matrix during cytokinesis. CHO1 was originally implicated in karyokinesis, but the invertebrate homologues of CHO1 were shown to function in the midzone formation and cytokinesis. To analyze the role of the protein in mammalian cells, we mutated the ATP-binding site of CHO1 and expressed it in CHO cells. Mutant protein (CHO1F′) was able to interact with microtubules via ATP-independent microtubule-binding site(s) but failed to accumulate at the midline of the central spindle and affected the localization of endogenous CHO1. Although the segregation of chromosomes, the bundling of midzone microtubules, and the initiation of cytokinesis proceeded normally in CHO1F′-expressing cells, the completion of cytokinesis was inhibited. Daughter cells were frequently entering interphase while connected by a microtubule-containing cytoplasmic bridge from which the dense midbody matrix was missing. Depletion of endogenous CHO1 via RNA-mediated interference also affected the formation of midbody matrix in dividing cells, caused the disorganization of midzone microtubules, and resulted in abortive cytokinesis. Thus, CHO1 may not be required for karyokinesis, but it is essential for the proper midzone/midbody formation and cytokinesis in mammalian cells.
机译:CHO1是MKLP1亚家族的哺乳动物驱动蛋白样运动蛋白。它在后期与纺锤体中部区结合,并在胞质分裂过程中浓缩为中体基质。 CHO1最初与核运动有关,但是CHO1的无脊椎动物同源物在中区形成和胞质分裂中起作用。为了分析蛋白质在哺乳动物细胞中的作用,我们突变了CHO1的ATP结合位点,并在CHO细胞中表达了它。突变蛋白(CHO1F')能够通过不依赖ATP的微管结合位点与微管相互作用,但无法在中心纺锤体的中线积聚并影响内源性CHO1的定位。尽管在表达CHO1F'的细胞中染色体分离,中区微管的束缚和胞质分裂的启动正常进行,但胞质分裂的完成受到抑制。子细胞经常进入相间,同时通过一个含有微管的胞质桥连接,而缺少稠密的中体基质。通过RNA介导的干扰消耗内源性CHO1也影响分裂细胞中体基质的形成,引起中区微管的混乱,并导致流产性胞质分裂。因此,CHO1不一定是核运动所必需的,但它对于哺乳动物细胞中适当的中区/中体形成和胞质分裂是必不可少的。

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