Vaucheret Hervé, Mallory Allison C, Bartel David P
Laboratoire de Biologie Cellulaire, Institut Jean-Pierre Bourgin, INRA, 78026 Versailles Cedex, France.
Mol Cell. 2006 Apr 7;22(1):129-36. doi: 10.1016/j.molcel.2006.03.011.
Arabidopsis ARGONAUTE1 (AGO1) encodes the RNA slicer enzyme of the microRNA (miRNA) pathway and is regulated by miR168-programmed, AGO1-catalyzed mRNA cleavage. Here, we describe two additional regulatory processes required for AGO1 homeostasis: transcriptional coregulation of MIR168 and AGO1 genes, and posttranscriptional stabilization of miR168 by AGO1. Disrupting any of these regulatory processes by using mutations or transgenes disturbs a proper functioning of the miRNA pathway. In contrast, minor perturbation leads to fine-tuned posttranscriptional adjustment of miR168 and AGO1 levels, thereby maintaining a proper balance of other miRNAs, which, together with AGO1, control the mRNA levels of miRNA targets. We suggest that miR168 stabilization occurs at the level of silencing-complex assembly and that modulating the efficiency of assembling miRNA-programmed silencing complexes will also be important in other contexts.
拟南芥AGO1(ARGONAUTE1)编码微小RNA(miRNA)途径的RNA切割酶,并受miR168编程的AGO1催化的mRNA切割调控。在此,我们描述了AGO1稳态所需的另外两个调控过程:MIR168和AGO1基因的转录共调控,以及AGO1对miR168的转录后稳定作用。通过使用突变或转基因破坏这些调控过程中的任何一个都会干扰miRNA途径的正常功能。相反,轻微扰动会导致miR168和AGO1水平的转录后微调,从而维持其他miRNA的适当平衡,这些miRNA与AGO1一起控制miRNA靶标的mRNA水平。我们认为miR168的稳定发生在沉默复合体组装水平,并且在其他情况下调节miRNA编程的沉默复合体的组装效率也很重要。