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PIWI Slicing and RNA Elements in Precursors Instruct Directional Primary piRNA Biogenesis

机译:PIWI切片和前体中的RNA元素指导定向的主要piRNA生物发生。

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PIWI proteins and PIWI-interacting RNAs (piRNAs) mediate repression of transposons in the animal gonads. Primary processing converts long single-stranded RNAs into ~30-nt piRNAs, but their entry into the biogenesis pathway is unknown. Here, we demonstrate that an RNA element at the 5' end of a piRNA cluster-which we termed piRNA trigger sequence (PTS)-can induce primary processing of any downstream sequence. We propose that such signals are triggers for the generation of the original pool of piRNAs. We also demonstrate that endonucleolytic cleavage of a transcript by a cytosolic PIWI results in its entry into primary processing, which triggers the generation of non-overlapping, contiguous primary piRNAs in the 3' direction from the target transcript. These piRNAs are loaded into a nuclear PIWI, thereby linking cytoplasmic post-transcriptional silencing to nuclear transcriptional repression.
机译:PIWI蛋白和PIWI相互作用RNA(piRNA)介导动物性腺中转座子的阻遏。初级加工将长的单链RNA转换为〜30 nt piRNA,但是它们进入生物发生途径尚不清楚。在这里,我们证明了位于piRNA簇5'端的RNA元件(我们称为piRNA触发序列(PTS))可以诱导任何下游序列的初级加工。我们建议,此类信号是piRNA原始库生成的触发因素。我们还证明,通过胞质PIWI进行转录本的内切核酸切割会导致其进入初级加工,从而触发从目标转录本沿3'方向生成不重叠,连续的初级piRNA。这些piRNA被加载到核PIWI中,从而将胞质转录后沉默与核转录抑制联系起来。

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