Centre National de la Recherche Scientifique, Institut de Génétique Humaine UPR1142, Montpellier, France.
Nat Struct Mol Biol. 2011 Mar;18(3):323-7. doi: 10.1038/nsmb.1987. Epub 2011 Feb 6.
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.
微小 RNA(miRNA)是一类小的非编码 RNA,通过转录后调控基因表达发挥作用。miRNA 表达的改变会强烈影响细胞的生理机能。在这里,我们在人类细胞中证明了 RNA 干扰(RNAi)机制的两个组成部分之间的交叉调控。抑制负责 pre-miRNA 输出的核输出蛋白 5(exportin-5),下调了 RNA 酶 III 所需的 pre-miRNA 成熟酶 Dicer 的表达。这种效应是转录后的,是由于 Dicer mRNA 的核定位增加所致。体外实验和细胞 RNA 免疫沉淀实验表明,exportin-5 与 Dicer mRNA 直接相互作用。通过过表达 pre-miRNA 或腺病毒 VA1 RNA 来滴定 exportin-5,导致 Dicer mRNA-exportin-5 相互作用的丧失和 Dicer 水平的降低。这种饱和也发生在腺病毒感染期间,并增强了病毒复制。我们的研究揭示了 pre-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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