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A Dicer-Independent Route for Biogenesis of siRNAs that Direct DNA Methylation in Arabidopsis

机译:拟南芥中直接DNA甲基化的siRNA生物合成的不依赖切丁机的途径。

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摘要

DNA methylation directed by 24-nucleotide (nt) small interfering RNAs (siRNAs) plays critical roles in gene regulation and transposon silencing in Arabidopsis. 24-nt siRNAs are known to be processed from double-stranded RNAs by Dicer-like 3 (DCL3) and loaded into the effector Argonaute 4 (AGO4). Here we report a distinct class of siRNAs independent of DCLs (sidRNAs). sidRNAs are present as ladders of similar to 20-60 nt in length, often having the same 50 ends but differing in 3' ends by 1-nt steps. We further show that sidRNAs are associated with AGO4 and capable of directing DNA methylation. Finally we show that sidRNA production depends on distributive 3'-5' exonucleases. Our findings suggest an alternative route for siRNA biogenesis. Precursor transcripts are bound by AGO4 and subsequently subjected to 3'-5' exonucleolytic trimming for maturation. We propose that sidRNAs generated through this route are the initial triggers of de novo DNA methylation.
机译:由24个核苷酸(nt)小干扰RNA(siRNA)指导的DNA甲基化在拟南芥中的基因调控和转座子沉默中起关键作用。已知24-nt siRNA是由Dicer-like 3(DCL3)从双链RNA加工而成的,并加载到效应子Argonaute 4(AGO4)中。在这里,我们报告了独立于DCL(sidRNA)的一类独特的siRNA。 sidRNAs的梯子长约20-60 nt,通常具有相同的50个末端,但3'末端相差1 nt。我们进一步表明sidRNAs与AGO4相关联并且能够指导DNA甲基化。最后,我们表明sidRNA的产生取决于3'-5'核酸外切酶。我们的发现提示了siRNA生物发生的另一种途径。前体转录物与AGO4结合,随后进行3'-5'核酸外切修饰以使其成熟。我们建议通过此途径生成的sidRNAs是从头DNA甲基化的最初触发条件。

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