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Dissection of the molecular mechanisms that control the nuclear accumulation of transport factors importin-alpha and CAS in stressed cells

机译:解剖控制应激细胞中转运因子importin-alpha和CAS核积累的分子机制

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摘要

The physiological state of eukaryotic cells controls nuclear trafficking of numerous cargos. For example, stress results in the inhibition of classical protein import, which is characterized by the redistribution of several transport factors. As such, importin-alpha and cellular apoptosis susceptibility protein (CAS) accumulate in nuclei of heat-shocked cells; however, the mechanisms underlying this relocation are not fully understood. We now show that heat upregulates the initial docking of importin-alpha at the nuclear envelope and stimulates the translocation of CAS into the nuclear interior. Moreover, heat exposure compromises the exit of importin-alpha from nuclei and drastically increases its retention in the nucleoplasm, whereas CAS nuclear exit and retention are less affected. Taken together, our results support the idea that heat shock regulates importin-alpha and CAS nuclear accumulation at several levels. The combination of different stress-induced changes leads to the nuclear concentration of both transport factors in heat-stressed cells.
机译:真核细胞的生理状态控制着许多货物的核运输。例如,压力导致经典蛋白质输入的抑制,其特征在于几种转运因子的重新分布。因此,importin-α和细胞凋亡敏感性蛋白(CAS)积聚在热激细胞的细胞核中。但是,这种重新定位的基础机制尚未完全了解。我们现在显示,热量上调了importin-alpha在核膜上的初始对接,并刺激了CAS进入核内部的转运。此外,热暴露会损害importin-α从核中的逸出,并大大增加其在核质中的保留,而CAS核的逸出和保留受到的影响较小。综上所述,我们的研究结果支持了热休克在几个水平上调节importin-alpha和CAS核积累的想法。不同的应力引起的变化的组合导致热应激细胞中两种转运因子的核浓缩。

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