Lee Heng-Chi, Chang Shwu-Shin, Choudhary Swati, Aalto Antti P, Maiti Mekhala, Bamford Dennis H, Liu Yi
Department of Physiology, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, Texas 75390, USA.
Nature. 2009 May 14;459(7244):274-7. doi: 10.1038/nature08041.
RNA interference pathways use small RNAs to mediate gene silencing in eukaryotes. In addition to small interfering RNAs (siRNAs) and microRNAs, several types of endogenously produced small RNAs have important roles in gene regulation, germ cell maintenance and transposon silencing. The production of some of these RNAs requires the synthesis of aberrant RNAs (aRNAs) or pre-siRNAs, which are specifically recognized by RNA-dependent RNA polymerases to make double-stranded RNA. The mechanism for aRNA synthesis and recognition is largely unknown. Here we show that DNA damage induces the expression of the Argonaute protein QDE-2 and a new class of small RNAs in the filamentous fungus Neurospora crassa. This class of small RNAs, known as qiRNAs because of their interaction with QDE-2, are about 20-21 nucleotides long (several nucleotides shorter than Neurospora siRNAs), with a strong preference for uridine at the 5' end, and originate mostly from the ribosomal DNA locus. The production of qiRNAs requires the RNA-dependent RNA polymerase QDE-1, the Werner and Bloom RecQ DNA helicase homologue QDE-3 and dicers. qiRNA biogenesis also requires DNA-damage-induced aRNAs as precursors, a process that is dependent on both QDE-1 and QDE-3. Notably, our results suggest that QDE-1 is the DNA-dependent RNA polymerase that produces aRNAs. Furthermore, the Neurospora RNA interference mutants show increased sensitivity to DNA damage, suggesting a role for qiRNAs in the DNA-damage response by inhibiting protein translation.
RNA干扰途径利用小RNA在真核生物中介导基因沉默。除了小干扰RNA(siRNA)和微小RNA外,几种内源性产生的小RNA在基因调控、生殖细胞维持和转座子沉默中发挥着重要作用。其中一些RNA的产生需要异常RNA(aRNA)或前体siRNA的合成,这些RNA被RNA依赖性RNA聚合酶特异性识别以形成双链RNA。aRNA合成和识别的机制在很大程度上尚不清楚。在这里,我们表明DNA损伤会诱导丝状真菌粗糙脉孢菌中AGO蛋白QDE-2和一类新的小RNA的表达。这类小RNA由于与QDE-2相互作用而被称为qiRNA,长度约为20-21个核苷酸(比粗糙脉孢菌的siRNA短几个核苷酸),在5'端强烈偏好尿苷,并且主要起源于核糖体DNA位点。qiRNA的产生需要RNA依赖性RNA聚合酶QDE-1、Werner和Bloom RecQ DNA解旋酶同源物QDE-3以及Dicer。qiRNA的生物合成还需要DNA损伤诱导的aRNA作为前体,这一过程依赖于QDE-1和QDE-3。值得注意的是,我们的结果表明QDE-1是产生aRNA的DNA依赖性RNA聚合酶。此外,粗糙脉孢菌RNA干扰突变体对DNA损伤表现出更高的敏感性,这表明qiRNA通过抑制蛋白质翻译在DNA损伤反应中发挥作用。