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首页> 外文期刊>Philosophical Transactions of the Royal Society of London, Series B. Biological Sciences >Arabidopsis RNA Polymerase IV generates 21-22 nucleotide small RNAs that can participate in RNA-directed DNA methylation and may regulate genes
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Arabidopsis RNA Polymerase IV generates 21-22 nucleotide small RNAs that can participate in RNA-directed DNA methylation and may regulate genes

机译:拟南芥RNA聚合酶IV产生21-22个核苷酸小RNA,可以参与RNA定向的DNA甲基化,并且可以调节基因

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摘要

The plant-specific RNA Polymerase IV (Pol IV) transcribes heterochromatic regions, including many transposable elements (TEs), with the well-described role of generating 24 nucleotide (nt) small interfering RNAs (siRNAs). These siRNAs target DNA methylation back to TEs to reinforce the boundary between heterochromatin and euchromatin. In the male gametophytic phase of the plant life cycle, pollen, Pol IV switches to generating primarily 21-22 nt siRNAs, but the biogenesis and function of these siRNAs have been enigmatic. In contrast to being pollen-specific, we identified that Pol IV generates these 21-22 nt siRNAs in sporophytic tissues, likely from the same transcripts that are processed into the more abundant 24 nt siRNAs. The 21-22 nt forms are specifically generated by the combined activities of DICER proteins DCL2/DCL4 and can participate in RNA-directed DNA methylation. These 21-22 nt siRNAs are also loaded into ARGONAUTE1 (AGO1), which is known to function in post-transcriptional gene regulation. Like other plant siRNAs and microRNAs incorporated into AGO1, we find a signature of genic mRNA cleavage at the predicted target site of these siRNAs, suggesting that Pol IV-generated 21-22 nt siRNAs may function to regulate gene transcript abundance. Our data provide support for the existing model that in pollen Pol IV functions in gene regulation.
机译:植物特异性RNA聚合酶IV(POL IV)转录异色区,包括许多可转换元素(TES),具有产生24个核苷酸(NT)小干扰RNA(siRNA)的良好描述的作用。这些siRNA靶向DNA甲基化回到TES以加强异铬胺和欧洲甜菜素之间的边界。在植物生命周期的雄性杂种阶段,Pollen,Pol IV切换到主要产生21-22 nt siRNA,但这些siRNA的生物发生和功能一直是神秘的。与花粉特异性相比,我们认为POL IV在孢子体组织中产生这21-22nt siRNA,可能是与加工成更丰富的24nt siRNA的相同转录物。 21-22NT形式由Dicer蛋白DCL2 / DCL4的组合活性特别产生,并且可以参与RNA定向的DNA甲基化。将这些21-22nt siRNA加载到Argonaute1(前1)中,该方法已知在转录后基因调节中起作用。与其他植物siRNA和microRNA一起掺入前1中,我们在这些siRNA的预测靶位点发现了基因mRNA切割的签名,表明POL IV产生的21-22NT siRNA可以起到调节基因转录物丰度。我们的数据为基因调节中的花粉POL IV功能提供了对现有模型的支持。

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