Cancer Research UK Cambridge Institute, University of Cambridge, Li Ka Shing Centre, Cambridge, CB2 0RE, UK.
Nat Commun. 2022 Apr 19;13(1):2118. doi: 10.1038/s41467-022-29787-3.
PIWI-interacting RNAs (piRNAs) are small RNAs required to recognize and silence transposable elements. The 5' ends of mature piRNAs are defined through cleavage of long precursor transcripts, primarily by Zucchini (Zuc). Zuc-dependent cleavage typically occurs immediately upstream of a uridine. However, Zuc lacks sequence preference in vitro, pointing towards additional unknown specificity factors. Here, we examine murine piRNAs and reveal a strong and specific enrichment of three sequences (UAA, UAG, UGA)-corresponding to stop codons-at piRNA 5' ends. Stop codon sequences are also enriched immediately after piRNA processing intermediates, reflecting their Zuc-dependent tail-to-head arrangement. Further analyses reveal that a Zuc in vivo cleavage preference at four sequences (UAA, UAG, UGA, UAC) promotes 5' end stop codons. This observation is conserved across mammals and possibly further. Our work provides new insights into Zuc-dependent cleavage and may point to a previously unrecognized connection between piRNA biogenesis and the translational machinery.
PIWI 相互作用 RNA(piRNAs)是识别和沉默转座元件所必需的小 RNA。成熟 piRNA 的 5' 端是通过长前体转录本的切割来定义的,主要由 Zucchini(Zuc)切割。Zuc 依赖性切割通常发生在尿嘧啶的上游。然而,Zuc 在体外缺乏序列偏好,这表明存在其他未知的特异性因素。在这里,我们研究了小鼠 piRNAs,并揭示了在 piRNA 5' 端强烈且特异性富集的三个序列(UAA、UAG、UGA)——对应于终止密码子。终止密码子序列也在 piRNA 加工中间体之后立即富集,反映了它们依赖 Zuc 的头对头排列。进一步的分析表明,Zuc 在体内对四个序列(UAA、UAG、UGA、UAC)的切割偏好促进了 5' 端终止密码子的产生。这一观察结果在哺乳动物中是保守的,可能在其他物种中也是如此。我们的工作为 Zuc 依赖性切割提供了新的见解,并可能指向 piRNA 生物发生和翻译机制之间以前未被认识到的联系。