Elvira-Matelot Emilie, Hachet Mélanie, Shamandi Nahid, Comella Pascale, Sáez-Vásquez Julio, Zytnicki Matthias, Vaucheret Hervé
Institut Jean-Pierre Bourgin, UMR 1318, INRA AgroParisTech CNRS, Université Paris-Saclay, 78000 Versailles, France.
URGI, INRA, 78000 Versailles, France.
Plant Cell. 2016 Feb;28(2):406-25. doi: 10.1105/tpc.15.00540. Epub 2016 Jan 13.
RNaseIII enzymes catalyze the cleavage of double-stranded RNA (dsRNA) and have diverse functions in RNA maturation. Arabidopsis thaliana RNASE THREE LIKE2 (RTL2), which carries one RNaseIII and two dsRNA binding (DRB) domains, is a unique Arabidopsis RNaseIII enzyme resembling the budding yeast small interfering RNA (siRNA)-producing Dcr1 enzyme. Here, we show that RTL2 modulates the production of a subset of small RNAs and that this activity depends on both its RNaseIII and DRB domains. However, the mode of action of RTL2 differs from that of Dcr1. Whereas Dcr1 directly cleaves dsRNAs into 23-nucleotide siRNAs, RTL2 likely cleaves dsRNAs into longer molecules, which are subsequently processed into small RNAs by the DICER-LIKE enzymes. Depending on the dsRNA considered, RTL2-mediated maturation either improves (RTL2-dependent loci) or reduces (RTL2-sensitive loci) the production of small RNAs. Because the vast majority of RTL2-regulated loci correspond to transposons and intergenic regions producing 24-nucleotide siRNAs that guide DNA methylation, RTL2 depletion modifies DNA methylation in these regions. Nevertheless, 13% of RTL2-regulated loci correspond to protein-coding genes. We show that changes in 24-nucleotide siRNA levels also affect DNA methylation levels at such loci and inversely correlate with mRNA steady state levels, thus implicating RTL2 in the regulation of protein-coding gene expression.
核糖核酸酶III(RNaseIII)催化双链RNA(dsRNA)的切割,并在RNA成熟过程中发挥多种功能。拟南芥RNASE THREE LIKE2(RTL2)携带一个RNaseIII和两个双链RNA结合(DRB)结构域,是一种独特的拟南芥RNaseIII酶,类似于出芽酵母中产生小干扰RNA(siRNA)的Dcr1酶。在这里,我们表明RTL2调节一小部分小RNA的产生,并且这种活性取决于其RNaseIII和DRB结构域。然而,RTL2的作用方式与Dcr1不同。虽然Dcr1直接将dsRNA切割成23个核苷酸的siRNA,但RTL2可能将dsRNA切割成长链分子,随后这些长链分子由类似Dicer的酶加工成小RNA。根据所考虑的dsRNA,RTL2介导的成熟过程要么提高(RTL2依赖位点)要么降低(RTL2敏感位点)小RNA的产生。由于绝大多数受RTL2调控的位点对应于产生指导DNA甲基化的24个核苷酸siRNA的转座子和基因间区域,RTL2的缺失会改变这些区域的DNA甲基化。尽管如此,13%的受RTL2调控的位点对应于蛋白质编码基因。我们表明,24个核苷酸siRNA水平的变化也会影响这些位点的DNA甲基化水平,并且与mRNA稳态水平呈负相关,从而表明RTL2参与蛋白质编码基因表达的调控。