Department of Developmental Biology, Sloan-Kettering Institute, New York, New York 10065, USA.
RNA. 2012 Dec;18(12):2166-73. doi: 10.1261/rna.036194.112. Epub 2012 Oct 24.
RNase III enzymes are fundamental to the biogenesis of microRNAs (miRNAs) and small interfering RNAs (siRNAs) in all species studied. Although alternative miRNA pathways independent of Drosha or Dicer exist, each still requires one RNase III-type enzyme. Here, we describe two strategies that marry either RNase Z or the Integrator complex with the slicing activity of Argonaute2 to generate highly functional mature miRNAs. We provide stringent validation of their RNase III independence by demonstrating efficient miRNA biogenesis and activity in Drosha and Dicer knockout cells. These data provide proof-of-principle evidence for additional mechanistic possibilities for efficient generation of small regulatory RNAs, and represent novel silencing triggers that may be exploited for technical purposes.
RNase III 酶是所有研究物种中小 RNA(miRNAs)和小干扰 RNA(siRNAs)生物发生的基础。尽管存在不依赖 Drosha 或 Dicer 的替代 miRNA 途径,但每种途径仍需要一种 RNase III 型酶。在这里,我们描述了两种将 RNase Z 或整合酶复合物与 Argonaute2 的切割活性相结合的策略,以生成具有高度功能的成熟 miRNAs。我们通过证明在 Drosha 和 Dicer 敲除细胞中有效进行 miRNA 生物发生和活性,严格验证了它们对 RNase III 的不依赖性。这些数据为有效生成小调控 RNA 的其他机制可能性提供了原理证明证据,并代表了可能用于技术目的的新型沉默触发物。