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Contractile ring-independent localization of DdINCENP, a protein important for spindle stability and cytokinesis

机译:DdINCENP的收缩环非依赖性定位,该蛋白对纺锤体稳定性和胞质分裂很重要

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Dictyostelium DdINCENP is a chromosomal passenger protein associated with centromeres, the spindle midzone, and poles during mitosis and the cleavage furrow during cytokinesis. Disruption of the single DdINCENP gene revealed important roles for this protein in mitosis and cytokinesis. DdINCENP null cells lack a robust spindle midzone and are hypersensitive to microtubule-depolymerizing drugs, suggesting that their spindles may not be stable. Furthermore DdCP224, a protein homologous to the microtubule-stabilizing protein TOGp/XMAP215, was absent from the spindle midzone of DdINCENP null cells. Overexpression of DdCP224 rescued the weak spindle midzone defect of DdINCENP null cells. Although not required for the localization of the myosin II contractile ring and subsequent formation of a cleavage furrow, DdINCENP is important for the abscission of daughter cells at the end of cytokinesis. Finally, we show that the localization of DdINCENP at the cleavage furrow is modulated by myosin II but it occurs by a mechanism different from that controlling the formation of the contractile ring.
机译:Dictyostelium DdINCENP是一种染色体过客蛋白,与着丝粒,纺锤体中区和有丝分裂期间的极点以及胞质分裂期间的分裂沟有关。单个DdINCENP基因的破坏揭示了该蛋白在有丝分裂和胞质分裂中的重要作用。 DdINCENP空细胞缺乏坚固的纺锤体中间区,并且对微管解聚药物非常敏感,表明它们的纺锤体可能不稳定。此外,DdINCENP空细胞的纺锤体中间区不存在与微管稳定蛋白TOGp / XMAP215同源的蛋白DdCP224。 DdCP224的过度表达挽救了DdINCENP空细胞的弱纺锤体中区缺陷。尽管对于肌球蛋白II收缩环的定位和随后的切割沟的形成不是必需的,但DdINCENP对于胞质分裂结束时子细胞的脱落很重要。最后,我们表明DdINCENP在卵裂沟中的定位是由肌球蛋白II调控的,但它的发生机制与控制收缩环形成的机制不同。

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