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A small RNA response at DNA ends in Drosophila

机译:果蝇DNA末端的小RNA反应

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Small RNAs have been implicated in numerous cellular processes, including effects on chromatin structure and the repression of transposons. We describe the generation of a small RNA response at DNA ends in Drosophila that is analogous to the recently reported double-strand break (DSB)-induced RNAs or Dicer- and Drosha-dependent small RNAs in Arabidopsis and vertebrates. Active transcription in the vicinity of the break amplifies this small RNA response, demonstrating that the normal messenger RNA contributes to the endogenous small interfering RNAs precursor. The double-stranded RNA precursor forms with an antisense transcript that initiates at the DNA break. Breaks are thus sites of transcription initiation, a novel aspect of the cellular DSB response. This response is specific to a double-strand break since nicked DNA structures do not trigger small RNA production. The small RNAs are generated independently of the exact end structure (blunt, 3′- or 5′-overhang), can repress homologous sequences in trans and may therefore—in addition to putative roles in repair—exert a quality control function by clearing potentially truncated messages from genes in the vicinity of the break.
机译:小RNA已经涉及许多细胞过程,包括对染色质结构的影响和转座子的抑制。我们描述了在果蝇的DNA末端的小RNA响应的生成,类似于最近报道的双链断裂(DSB)诱导的RNA或拟南芥和脊椎动物中依赖Dicer和Drosha的小RNA。断裂附近的主动转录放大了这种小RNA反应,表明正常的信使RNA有助于内源性小干扰RNA前体。双链RNA前体形成带有在DNA断裂处起始的反义转录物。因此,断裂是转录起始的位点,是细胞DSB反应的一个新方面。该反应是特异于双链断裂的,因为有切口的DNA结构不会触发小RNA的产生。小RNA的产生与确切的末端结构(钝的,3'-或5'-突出端)无关,可以反式阻遏同源序列,因此,除了假定的修复作用外,还可以通过清除潜在的核酸来发挥质量控制功能中断附近基因的截短消息。

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