Center for RNA Biology: From Genome to Therapeutics, Department of Biochemistry and Biophysics, University of Rochester Medical Center, Rochester, NY, USA.
Computational Biology Department, Carnegie Mellon University, Pittsburgh, PA, USA.
Nat Cell Biol. 2020 Feb;22(2):200-212. doi: 10.1038/s41556-019-0457-4. Epub 2020 Feb 3.
PIWI-interacting RNAs (piRNAs) are a class of small non-coding RNAs essential for fertility. In adult mouse testes, most piRNAs are derived from long single-stranded RNAs lacking annotated open reading frames (ORFs). The mechanisms underlying how piRNA sequences are defined during the cleavages of piRNA precursors remain elusive. Here, we show that 80S ribosomes translate the 5'-proximal short ORFs (uORFs) of piRNA precursors. The MOV10L1/Armitage RNA helicase then facilitates the translocation of ribosomes into the uORF downstream regions (UDRs). The ribosome-bound UDRs are targeted by piRNA processing machinery, with the processed ribosome-protected regions becoming piRNAs. The dual modes of interaction between ribosomes and piRNA precursors underlie the distinct piRNA biogenesis requirements at uORFs and UDRs. Ribosomes also mediate piRNA processing in roosters and green lizards, implying that this mechanism is evolutionarily conserved in amniotes. Our results uncover a function for ribosomes on non-coding regions of RNAs and reveal the mechanisms underlying how piRNAs are defined.
PIWI 相互作用 RNA(piRNAs)是一类对于生育至关重要的小非编码 RNA。在成年小鼠的睾丸中,大多数 piRNAs 来源于缺乏注释开放阅读框(ORF)的长单链 RNA。piRNA 前体切割过程中 piRNA 序列如何被定义的机制仍不清楚。在这里,我们表明 80S 核糖体翻译 piRNA 前体的 5'-近端短 ORF(uORF)。然后,MOV10L1/Armitage RNA 解旋酶促进核糖体进入 uORF 下游区域(UDR)的易位。核糖体结合的 UDR 被 piRNA 加工机制靶向,经过加工的核糖体保护区域成为 piRNAs。核糖体与 piRNA 前体之间的两种相互作用模式为 uORF 和 UDR 处不同的 piRNA 生物发生要求提供了基础。核糖体还介导了公鸡和绿蜥蜴中的 piRNA 加工,这表明该机制在羊膜动物中是进化保守的。我们的结果揭示了核糖体在 RNA 的非编码区域的功能,并揭示了 piRNAs 如何被定义的机制。