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DDX3 Regulates Cell Growth through Translational Control of Cyclin E1

机译:DDX3通过细胞周期蛋白E1的翻译控制来调节细胞的生长。

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摘要

DDX3 belongs to the DEAD box family of RNA helicases, but the details of its biological function remain largely unclear. Here we show that knockdown of DDX3 expression impedes G1/S-phase transition of the cell cycle. To know how DDX3 may act in cell cycle control, we screened for cellular mRNA targets of DDX3. Many of the identified DDX3 targets encoded cell cycle regulators, including G1/S-specific cyclin E1. DDX3 depletion specifically downregulates translation of cyclin E1 mRNA. Moreover, our data suggest that DDX3 participates in translation initiation of targeted mRNAs as well as in cell growth control via its RNA helicase activity. Consistent with these findings, we show that in the temperature-sensitive DDX3 mutant hamster cell line tsET24, cyclin E1 expression is downregulated at a nonpermissive temperature that inactivates mutant DDX3. Taken together, our results indicate that DDX3 is critical for translation of cyclin E1 mRNA, which provides an alternative mechanism for regulating cyclin E1 expression during the cell cycle.
机译:DDX3属于DEAD盒RNA解旋酶家族,但其生物学功能的细节仍不清楚。在这里,我们显示了DDX3表达的敲低阻碍了细胞周期的G1 / S期过渡。要知道DDX3如何在细胞周期控制中起作用,我们筛选了DDX3的细胞mRNA靶标。许多已确定的DDX3靶向编码细胞周期调节剂,包括G1 / S特异性细胞周期蛋白E1。 DDX3耗竭专门下调细胞周期蛋白E1 mRNA的翻译。此外,我们的数据表明DDX3通过其RNA解旋酶活性参与了靶向mRNA的翻译起始以及细胞生长控制。与这些发现一致,我们表明在温度敏感的DDX3突变仓鼠细胞系tsET24中,细胞周期蛋白E1的表达在使突变DDX3失活的非容许温度下被下调。两者合计,我们的结果表明DDX3对于细胞周期蛋白E1 mRNA的翻译至关重要,这为细胞周期中细胞周期蛋白E1表达的调节提供了另一种机制。

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