首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >piRNA-mediated nuclear accumulation of retrotransposon transcripts in the Drosophila female germline
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piRNA-mediated nuclear accumulation of retrotransposon transcripts in the Drosophila female germline

机译:piRNA介导的果蝇雌性种系中反转录转座子转录本的核积累

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摘要

Germline silencing of transposable elements is essential for the maintenance of genome integrity. Recent results indicate that this repression is largely achieved through a RNA silencing pathway that involves Piwi-interacting RNAs (piRIMAs). However the repressive mechanisms are not well understood. To address this question, we used the possibility to disrupt the repression of the Drosophila I element retrotransposon by hybrid dysgenesis. We show here that the repression of the functional I elements that are located in euchromatin requires proteins of the piRNA pathway, and that the amount of ovarian I element piRNAs correlates with the strength of the repression in the female germline. Antisense RNAs, which are likely used to produce antisense piRNAs, are transcribed by heterochromatic defective I elements, but efficient production of these antisense small RNAs requires the presence in the genome of euchromatic functional I elements. Finally, we demonstrate that the piRNA-induced silencing of the functional I elements is at least partially posttranscriptional. In a repressive background, these elements are still transcribed, but some of their sense transcripts are kept in nurse cell nuclear foci together with those of the Doc retrotransposon. In the absence of I element piRNAs, either in dysgenic females or in mutants of the piRNA silencing pathway, sense I element transcripts are transported toward the oocyte where retrotransposition occurs. Our results indicate that piRNAs are involved in a posttranscriptional gene-silencing mechanism resulting in RNA nuclear accumulation.
机译:转座子的种系沉默对于维持基因组完整性至关重要。最近的结果表明,这种抑制作用很大程度上是通过涉及Piwi相互作用RNA(piRIMAs)的RNA沉默途径实现的。然而,抑制机制还没有被很好地理解。为了解决这个问题,我们使用了通过杂种发育不全来破坏果蝇I元件反转录转座子的可能性。我们在这里显示,位于常染色质中的功能性I元件的抑制需要piRNA途径的蛋白质,并且卵巢I元件piRNA的数量与雌性种系中的抑制强度相关。可能用于产生反义piRNA的反义RNA被异色缺陷I元件转录,但是要有效生产这些反义小RNA,需要在基因组中存在常染色体功能性I元件。最后,我们证明了piRNA诱导的功能性I元件沉默至少部分在转录后。在压抑的背景下,这些元件仍被转录,但它们的某些有义转录本与Doc逆转录转座子的转录本一起保存在护士细胞核灶中。在雌激素缺乏或piRNA沉默途径突变体中不存在I元素piRNA的情况下,有义I元素转录物会向发生逆转座的卵母细胞转运。我们的结果表明,piRNA参与转录后基因沉默机制,导致RNA核积累。

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