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A rADAR defense against RNAi

机译:对RNAi的雷达防守

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摘要

Adenosine deaminases that act on RNA (ADARs) convert adenosines (A) to inosines (I) in stretches of dsRNA. The biological purpose of these editing events for the vast majority of ADAR substrates is largely unknown. In this issue of Genes & Development, Reich and colleagues (pp. 271-282) demonstrate that in Caenorhabditis elegans, A-to-I editing in double-stranded regions of protein-coding transcripts protects these RNAs from targeting by the RNAi pathway. Disruption of this safeguard through loss of ADAR activity coupled with enhanced RNAi results in developmental abnormalities and profound changes in gene expression that suggest aberrant induction of an antiviral response. Thus, editing of cellular dsRNA by ADAR helps prevent host RNA silencing and inadvertent antiviral activity.
机译:在RNA(ADARS)上作用的腺苷脱氨酶将腺苷(a)转化为DsRNA延伸的毒素(I)。 绝大多数ADAR基材的这些编辑事件的生物目的主要是未知的。 在这个问题和同事(第271-282页)的基因和发展问题中,证明,在Caenorhabditis elegiss中,在蛋白质编码转录物的双链区域中的A-to-I编辑保护这些RNA通过RNAI途径靶向。 通过损失与增强的RNAI丧失的ADAR活性破坏这种保障导致产生异常和基因表达的深刻变化,提示异常诱导抗病毒反应。 因此,ADAR的细胞DSRNA的编辑有助于预防宿主RNA沉默和无意的抗病毒活性。

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