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5AC3 may link nuclear protein export to cell cycle progression

机译:5AC3可能将核蛋白输出与细胞周期进程联系起来

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摘要

Seledive movement of proteins between the nucleus and the Cytoplasm is a regulatory mechanism exploited extensively by the eukaryotic cell. We have identified the evolutionarily conserved Sac3 protein, which was implicated previously in the regulation of mitosis IBauer, A. & K6lling. R. (1996),. Cell Sci 109, 1 S75--1583l as a novel mediator of nuclear protein export. We show that Sacep is localized to the nuclear pore, where it interacts with nucleoporins. Loss of SAC3 function results in a block in nuclear export of a nuclear export signal-containing reporter protein. Our results also demonstrate that SAC3 interacts genetically with the nuclear protein export factors Crm1p/Xpo1p and Yrb2p. Taken together, these data indicate a link between nuclear protein export and transition through the cell cycle.
机译:蛋白质在细胞核和细胞质之间的迁移是一种被真核细胞广泛利用的调节机制。我们已经鉴定了进化上保守的Sac3蛋白,该蛋白先前与有丝分裂IBauer,A。&K6lling的调控有关。 R.(1996)。 Cell Sci 109,1 S75--1583l是核蛋白输出的新型介体。我们显示,Sacep定位于核孔,与核孔蛋白相互作用。 SAC3功能的丧失导致含有核输出信号的报告蛋白的核输出受阻。我们的结果还表明,SAC3与核蛋白输出因子Crm1p / Xpo1p和Yrb2p发生遗传相互作用。综上所述,这些数据表明核蛋白输出与整个细胞周期过渡之间存在联系。

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