Mallory Allison C, Vaucheret Hervé
Laboratoire de Biologie Cellulaire, Institut Jean-Pierre Bourgin, INRA, Route de Saint-Cyr, 78026 Versailles, France.
EMBO Rep. 2009 May;10(5):521-6. doi: 10.1038/embor.2009.32. Epub 2009 Apr 3.
ARGONAUTE 1 (AGO1) slices endogenous messenger RNAs (mRNAs) during both microRNA (miRNA)- and short interfering RNA (siRNA)-guided post-transcriptional silencing. We have previously reported that AGO1 homeostasis is maintained through the repressive action of miR168 on AGO1 mRNA and the stabilizing effect of AGO1 protein on miR168, but siRNA-mediated AGO1 regulation has not been reported. Here, we show that AGO1-derived siRNAs trigger RNA DEPENDENT RNA POLYMERASE 6 (RDR6)-, SUPPRESSOR OF GENE SILENCING 3 (SGS3)- and SILENCING DEFECTIVE 5 (SDE5)-dependent AGO1 silencing, which also requires DICER-LIKE 2 (DCL2) and DCL4. By varying the efficacy of miR168-guided AGO1 mRNA cleavage, we show that siRNA-mediated AGO1 silencing depends on correct miRNA targeting, pointing to coordinated regulatory actions of the miRNA and siRNA pathways during the maintenance of AGO1 homeostasis. Finally, our results reveal that dcl2, dcl3 and dcl4 mutations similarly affect post-transcriptional gene silencing (PTGS) mediated by a sense transgene and PTGS mediated by inverted repeats, validating the branched pathway model proposed previously.
在微小RNA(miRNA)和小干扰RNA(siRNA)介导的转录后沉默过程中,AGO1(精氨酸酶1)会切割内源性信使核糖核酸(mRNA)。我们之前曾报道,miR168通过对AGO1 mRNA的抑制作用以及AGO1蛋白对miR168的稳定作用来维持AGO1的稳态,但尚未有关于siRNA介导的AGO1调控的报道。在此,我们表明AGO1衍生的siRNA会触发依赖于RNA的RNA聚合酶6(RDR6)、基因沉默抑制因子3(SGS3)和沉默缺陷因子5(SDE5)的AGO1沉默,这一过程还需要类Dicer酶2(DCL2)和DCL4。通过改变miR168引导的AGO1 mRNA切割效率,我们发现siRNA介导的AGO1沉默依赖于正确的miRNA靶向作用,这表明在维持AGO1稳态过程中,miRNA和siRNA途径存在协同调控作用。最后,我们的结果表明,dcl2、dcl3和dcl4突变同样会影响由正义转基因介导的转录后基因沉默(PTGS)以及由反向重复序列介导的PTGS,验证了之前提出的分支途径模型。