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Sorting of small RNAs into Arabidopsis argonaute complexes is directed by the 5 ' terminal nucleotide

机译:将小RNA分为拟南芥的复杂复合体是由5'末端核苷酸指导的

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Argonaute (AGO) proteins recruit small RNAs to form the core of RNAi effector complexes. Arabidopsis encodes ten AGO proteins and a large network of small RNAs. How these small RNAs are sorted into specific AGO complexes remains largely unknown. We have cataloged small RNAs resident in four AGO complexes. We found that AGO2 and AGO4 preferentially recruit small RNAs with a 5 ' terminal adenosine, whereas AGO1 harbors microRNAs (miRNAs) that favor a 5 ' terminal uridine. AGO5 predominantly binds small RNAs that initiate with cytosine. Changing the 5 ' terminal nucleotide of an miRNA predictably redirected it into a different AGO complex and alters its biological activity. These results reveal a role for small RNA sequences in assorting among AGO complexes. This suggests that specialization of AGO complexes might involve remodeling the 5 ' end-binding pocket to accept certain small RNA sequences, perhaps explaining the evolutionary drive for miRNAs to initiate with uridine.
机译:Argonaute(AGO)蛋白募集小RNA,以形成RNAi效应子复合物的核心。拟南芥编码十种AGO蛋白和一个由小RNA组成的大型网络。这些小RNA如何被分类成特定的AGO复合物仍然是未知的。我们已经对驻留在四个AGO复合物中的小RNA进行了分类。我们发现AGO2和AGO4优先募集具有5'末端腺苷的小RNA,而AGO1则保留了支持5'末端尿苷的microRNA(miRNA)。 AGO5主要结合以胞嘧啶起始的小RNA。改变miRNA的5'末端核苷酸可预测地将其重定向到其他AGO复合物中,并改变其生物学活性。这些结果揭示了小RNA序列在AGO复合物中的分类中的作用。这表明AGO复合物的专业化可能涉及重塑5'末端结合口袋以接受某些小RNA序列,这也许可以解释miRNA从尿苷起始的进化驱动力。

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