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Competition for XPO5 binding between Dicer mRNA, pre-miRNA and viral RNA regulates human Dicer levels

机译:Dicer mRNA,pre-miRNA和病毒RNA之间XPO5结合的竞争调节了人类Dicer的水平

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MicroRNAs (miRNAs) are a class of small, noncoding RNAs that function by regulating gene expression post-transcriptionally. Alterations in miRNA expression can strongly influence cellular physiology. Here we demonstrated cross-regulation between two components of the RNA interference (RNAi) machinery in human cells. Inhibition of exportin-5, the karyopherin responsible for pre-miRNA export, downregulated expression of Dicer, the RNase III required for pre-miRNA maturation. This effect was post-transcriptional and resulted from an increased nuclear localization of Dicer mRNA. In vitro assays and cellular RNA immunoprecipitation experiments showed that exportin-5 interacted directly with Dicer mRNA. Titration of exportin-5 by overexpression of either pre-miRNA or the adenoviral VA1 RNA resulted in loss of Dicer mRNA-exportin-5 interaction and reduction of Dicer level. This saturation also occurred during adenoviral infection and enhanced viral replication. Our study reveals an important cross-regulatory mechanism between pre-miRNA or viral small RNAs and Dicer through exportin-5.
机译:MicroRNA(miRNA)是一类小的非编码RNA,可通过转录后调控基因表达发挥功能。 miRNA表达的改变会强烈影响细胞生理。在这里,我们证明了人类细胞中RNA干扰(RNAi)机制的两个组件之间的交叉调节。抑制出口蛋白5(负责pre-miRNA出口的核仁蛋白)抑制Dicer(pre-miRNA成熟所需的RNase III)的表达。这种作用是转录后的,并且是由于Dicer mRNA的核定位增加所致。体外测定和细胞RNA免疫沉淀实验表明,exportin-5与Dicer mRNA直接相互作用。通过pre-miRNA或腺病毒VA1 RNA的过表达滴定exportin-5导致Dicer mRNA-exportin-5相互作用的丧失和Dicer水平的降低。在腺病毒感染和病毒复制增强期间也发生了这种饱和。我们的研究揭示了前miRNA或病毒小RNA与Dicer之间通过exportin-5的重要交叉调控机制。

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