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Depletion of nucleophosmin leads to distortion of nucleolar and nuclear structures in HeLa cells

机译:核磷蛋白的消耗导致HeLa细胞中核仁和核结构的变形

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摘要

NPM (nucleophosmin; also known as B23) is an abundantly and ubiquitously expressed multifunctional nucleolar phosphoprotein, which is involved in numerous cellular processes, including ribosome biogenesis, protein chaperoning and centrosome duplication; however, the role of NPM in the cell cycle still remains unknown. In the present study, we show dynamic localization of NPM throughout the cell cycle of HeLa cells. Using a combination of RNAi (RNA interference) and three-dimensional microscopy we show that NPM is localized at the chromosome periphery during mitosis. We also demonstrate that depletion of NPM causes distortion of nucleolar structure as expected and leads to unexpected dramatic changes in nuclear morphology with multiple micronuclei formation. The defect in nuclear shape of NPM-depleted cells, which is clearly observed by live-cell imaging, is due to the distortion of cytoskeletal (α-tubulin and β-actin) structure, resulting from the defects in centrosomal microtubule nucleation. These results indicate that NPM is an essential protein not only for the formation of normal nucleolar structure, but also for the maintenance of regular nuclear shape in HeLa cells.
机译:NPM(nucleophosmin;也称为B23)是一种广泛表达的多功能核仁磷酸化蛋白,它参与许多细胞过程,包括核糖体生物发生,蛋白伴侣和中心体复制。然而,NPM在细胞周期中的作用仍然未知。在本研究中,我们显示了整个HeLa细胞的细胞周期中NPM的动态定位。使用RNAi(RNA干扰)和三维显微镜的组合,我们显示NPM在有丝分裂过程中位于染色体外围。我们还证明,NPM的耗竭会导致核仁结构变形,并会导致核形态发生意外的剧烈变化,并形成多个微核。通过活细胞成像可以清楚地观察到耗尽NPM的细胞核形状的缺陷,这是由于中心体微管成核缺陷导致的细胞骨架(α-微管蛋白和β-肌动蛋白)结构变形所致。这些结果表明,NPM不仅是正常核仁结构形成的必需蛋白,而且对于维持HeLa细胞的规则核形状也是必需的。

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