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Importin-beta facilitates nuclear import of human GW proteins and balances cytoplasmic gene silencing protein levels

机译:Importin-beta有助于人类GW蛋白的核输入并平衡细胞质基因沉默蛋白水平

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摘要

MicroRNAs (miRNAs) guide Argonaute (Ago) proteins to distinct target mRNAs leading to translational repression and mRNA decay. Ago proteins interact with a member of the GW protein family, referred to as TNRC6A-C in mammals, which coordinate downstream gene-silencing processes. The cytoplasmic functions of TNRC6 and Ago proteins are reasonably well established. Both protein families are found in the nucleus as well. Their detailed nuclear functions, however, remain elusive. Furthermore, it is not clear which import routes Ago and TNRC6 proteins take into the nucleus. Using different nuclear transport assays, we find that Ago as well as TNRC6 proteins shuttle between the cytoplasm and the nucleus. While import receptors might function redundantly to transport Ago2, we demonstrate that TNRC6 proteins are imported by the Importin-beta pathway. Finally, we show that nuclear localization of both Ago2 and TNRC6 proteins can depend on each other suggesting actively balanced cytoplasmic Ago - TNRC6 levels.
机译:MicroRNA(miRNA)将Argonaute(Ago)蛋白引导至不同的靶标mRNA,从而导致翻译抑制和mRNA降解。前蛋白与哺乳动物中称为TNRC6A-C的GW蛋白家族成员相互作用,从而协调下游基因沉默过程。 TNRC6和Ago蛋白的细胞质功能已得到很好的确立。两种蛋白质家族也都在细胞核中发现。但是,它们的详细核功能仍然难以捉摸。此外,尚不清楚Ago和TNRC6蛋白通过哪种进口途径进入细胞核。使用不同的核转运分析,我们发现Ago以及TNRC6蛋白在细胞质和细胞核之间穿梭。虽然进口受体可能在转运Ago2方面发挥冗余作用,但我们证明TNRC6蛋白是通过Importin-beta途径进口的。最后,我们表明Ago2和TNRC6蛋白的核定位可以相互依赖,这提示了主动平衡的细胞质Ago-TNRC6水平。

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