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The DEAD-box helicase DDX3 substitutes for the cap-binding protein eIF4E to promote compartmentalized translation initiation of the HIV-1 genomic RNA

机译:DEAD-box解旋酶DDX3替代了帽结合蛋白eIF4E,以促进HIV-1基因组RNA的区室化翻译起始

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Here, we show a novel molecular mechanism promoted by the DEAD-box RNA helicase DDX3 for translation of the HIV-1 genomic RNA. This occurs through the adenosine triphosphate-dependent formation of a translation initiation complex that is assembled at the 5′ m7GTP cap of the HIV-1 mRNA. This is due to the property of DDX3 to substitute for the initiation factor eIF4E in the binding of the HIV-1 m7GTP 5′ cap structure where it nucleates the formation of a core DDX3/PABP/eIF4G trimeric complex on the HIV-1 genomic RNA. By using RNA fluorescence in situ hybridization coupled to indirect immunofluorescence, we further show that this viral ribonucleoprotein complex is addressed to compartmentalized cytoplasmic foci where the translation initiation complex is assembled.
机译:在这里,我们显示了DEAD-box RNA解旋酶DDX3促进HIV-1基因组RNA翻译的新型分子机制。这是通过翻译起始复合物的三磷酸腺苷依赖性形成而发生的,该复合物在HIV-1 mRNA的5'm 7 GTP帽处组装。这是由于DDX3在HIV-1 m 7 GTP 5'帽结构的结合中取代了起始因子eIF4E的特性,在其中它使核心DDX3 / PABP / eIF4G的形成成核HIV-1基因组RNA上的三聚体复合物。通过使用耦合到间接免疫荧光的RNA荧光原位杂交,我们进一步表明,这种病毒核糖核蛋白复合物被定位到组装了翻译起始复合物的分隔的细胞质灶。

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