体外siRNA生物发生的重构:RNA定向DNA甲基化途径中的新反应机制和RNA通道。

Jasleen Singh, Craig S Pikaard
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引用次数: 12

摘要

真核生物利用rna介导的基因沉默途径来保护它们的基因组免受转座因子和入侵病毒等自私遗传因子的侵害。在植物中,rna定向DNA甲基化(RdDM)用于在转录水平上沉默自私元件。这一过程涉及24nt短干扰rna (sirna)和sirna碱基对的较长非编码rna。最近,我们发现24-nt siRNA的生物发生可以用纯化酶在试管中重现,为之前的遗传和基因组研究未解决的许多问题提供了生化答案。有趣的是,每种酶都具有控制下一步发生的事情的活性,从而引导RdDM途径内的rna并限制它们转移到其他途径。然而,对RdDM途径的其他重要步骤缺乏类似的机制理解。我们讨论了一些最需要生化研究的步骤和仍然需要回答的重要问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Reconstitution of siRNA Biogenesis In Vitro: Novel Reaction Mechanisms and RNA Channeling in the RNA-Directed DNA Methylation Pathway.

Eukaryotes deploy RNA-mediated gene silencing pathways to guard their genomes against selfish genetic elements, such as transposable elements and invading viruses. In plants, RNA-directed DNA methylation (RdDM) is used to silence selfish elements at the level of transcription. This process involves 24-nt short interfering RNAs (siRNAs) and longer noncoding RNAs to which the siRNAs base-pair. Recently, we showed that 24-nt siRNA biogenesis could be recapitulated in the test tube using purified enzymes, yielding biochemical answers to numerous questions left unresolved by prior genetic and genomic studies. Interestingly, each enzyme has activities that program what happens in the next step, thus channeling the RNAs within the RdDM pathway and restricting their diversion into alternative pathways. However, a similar mechanistic understanding is lacking for other important steps of the RdDM pathway. We discuss some of the steps most in need of biochemical investigation and important questions still in need of answers.

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