Diederichs Sven, Haber Daniel A
Massachusetts General Hospital Cancer Center, Harvard Medical School, Charlestown, MA 02129, USA.
Cell. 2007 Dec 14;131(6):1097-108. doi: 10.1016/j.cell.2007.10.032.
MicroRNAs are small endogenous noncoding RNAs involved in posttranscriptional gene regulation. During microRNA biogenesis, Drosha and Dicer process the primary transcript (pri-miRNA) through a precursor hairpin (pre-miRNA) to the mature miRNA. The miRNA is incorporated into the RNA-Induced Silencing Complex (RISC) with Argonaute proteins, the effector molecules in RNA interference (RNAi). Here, we show that all Argonautes elevate mature miRNA expression posttranscriptionally, independent of RNase activity. Also, we identify a role for the RISC slicer Argonaute2 (Ago2) in cleaving the pre-miRNA to an additional processing intermediate, termed Ago2-cleaved precursor miRNA or ac-pre-miRNA. This endogenous, on-pathway intermediate results from cleavage of the pre-miRNA hairpin 12 nucleotides from its 3'-end. By analogy to siRNA processing, Ago2 cleavage may facilitate removal of the nicked passenger strand from RISC after maturation. The multiple roles of Argonautes in the RNAi effector phase and miRNA biogenesis and maturation suggest coordinate regulation of microRNA expression and function.
微小RNA是参与转录后基因调控的内源性非编码小RNA。在微小RNA生物合成过程中,Drosha和Dicer通过前体发夹(前体微小RNA)将初级转录本(初级微小RNA)加工成成熟的微小RNA。微小RNA与AGO蛋白一起被整合到RNA诱导沉默复合体(RISC)中,AGO蛋白是RNA干扰(RNAi)中的效应分子。在此,我们表明,所有AGO蛋白均在转录后提高成熟微小RNA的表达,且与核糖核酸酶活性无关。此外,我们确定了RISC切割酶AGO2在将前体微小RNA切割成另一种加工中间体(称为AGO2切割的前体微小RNA或ac-前体微小RNA)中的作用。这种内源性的、途径中的中间体是由前体微小RNA发夹从其3'端切割12个核苷酸产生的。类似于小干扰RNA的加工过程,AGO2切割可能有助于在成熟后从RISC中去除带切口的过客链。AGO蛋白在RNAi效应阶段以及微小RNA生物合成和成熟中的多种作用表明微小RNA表达和功能存在协同调控。