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MicroRNA-Targeted and Small Interfering RNA-Mediated mRNA Degradation Is Regulated by Argonaute, Dicer, and RNA-Dependent RNA Polymerase in Arabidopsis

机译:MicroRNA靶向和小干扰RNA介导的mRNA降解是由拟南芥中的Argonaute,Dicer和RNA依赖性RNA聚合酶调节的。

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摘要

ARGONAUTE1 (AGO1) of Arabidopsis thaliana mediates the cleavage of microRNA (miRNA)-targeted mRNAs, and it has also been implicated in the posttranscriptional silencing of transgenes and the maintenance of chromatin structure. Mutations in AGO1 severely disrupt plant development, indicating that miRNA function and possibly other aspects of RNA interference are essential for maintaining normal patterns of gene expression. Using microarrays, we found that 1 to 6% of genes display significant expressionchanges in several alleles of ago1 at multiple developmental stages, with the majority showing higher levels. Several classes of known miRNA targets increased markedly in ago1, whereas others showed little or no change. Cleavage of mRNAs within miRNA-homologous sites was reduced but not abolished in an ago1 -null background, indicating that redundant slicer activity exists in Arabidopsis. Small interfering RNAs and larger 30- to 60-nucleotide RNA fragments corresponding to highly upregulated miRNA target genes accumulated in wild-type plants but not in ago1, the RNA-dependent RNA polymerase mutants rdr2 and rdr6, or the Dicer-like mutants dcl1 and dcl3. Both sense and antisense RNAs corresponding to these miRNA targets accumulated in the ago1 and dcl1 backgrounds. These results indicate that a subset of endogenous mRNA targets of RNA interference may be regulated through a mechanism of second-strand RNA synthesis and degradation initiated by or in addition to miRNA-mediated cleavage.
机译:拟南芥的ARGONAUTE1(AGO1)介导了针对microRNA(miRNA)的mRNA的切割,并且还涉及转基因的转录后沉默和染色质结构的维持。 AGO1中的突变严重破坏了植物的发育,表明miRNA的功能以及RNA干扰的其他方面可能对于维持基因表达的正常模式至关重要。使用微阵列,我们发现1至6%的基因在多个发育阶段的ago1的几个等位基因中显示出显着的表达变化,而大多数则显示出更高的水平。几类已知的miRNA靶标在年前显着增加,而其他几类则显示很少或没有变化。 miRNA同源位点内的mRNA切割减少,但在过去没有背景的情况下没有消除,表明拟南芥中存在多余的切片机活性。与野生型植物中积累的高度上调的miRNA靶基因相对应的小干扰RNA和30至60个核苷酸的较大RNA片段,但不是在过去1,依赖RNA的RNA聚合酶突变体rdr2和rdr6或类似Dicer的突变体dcl1和dcl3。对应于这些miRNA靶标的有义和反义RNA都积累在ago1和dcl1背景中。这些结果表明,RNA干扰的内源性mRNA靶标的子集可以通过由miRNA介导的裂解或除了miRNA介导的裂解而引发的第二链RNA合成和降解的机制来调节。

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