Department of Biology, Syracuse University, 107 College Place, Syracuse, NY 13244, USA.
Computational Biology Unit, Department of Informatics, University of Bergen, 5008 Bergen, Norway.
Genetics. 2024 Oct 7;228(2). doi: 10.1093/genetics/iyae120.
Terminal nucleotidyltransferases add nucleotides to the 3' end of RNA to modify their stability and function. In Caenorhabditis elegans, the terminal uridyltransferases/poly(U) polymerases PUP-1 (aka CID-1, CDE-1), PUP-2, and PUP-3 affect germline identity, survival, and development. Here, we identify small RNA (sRNA) and mRNA targets of these PUPs and of a fourth predicted poly(U) polymerase, F43E2.1/PUP-4. Using genetic and RNA sequencing approaches, we identify RNA targets of each PUP and the U-tail frequency and length of those targets. At the whole organism level, PUP-1 is responsible for most sRNA U-tailing, and other PUPs contribute to modifying discrete subsets of sRNAs. Moreover, the expression of PUP-2, PUP-3, and especially PUP-4 limits uridylation on some sRNAs. The relationship between uridylation status and sRNA abundance suggests that U-tailing can have a negative or positive effect on abundance depending on context. sRNAs modified by PUP activity primarily target mRNAs that are ubiquitously expressed or most highly expressed in the germline. mRNA data obtained with a Nanopore-based method reveal that the addition of U-tails to nonadenylated mRNA is substantially reduced in the absence of PUP-3. Overall, this work identifies PUP RNA targets, defines the effect of uridylation loss on RNA abundance, and reveals the complexity of PUP regulation in C. elegans development.
末端核苷酸转移酶将核苷酸添加到 RNA 的 3' 端,以修饰其稳定性和功能。在秀丽隐杆线虫中,末端尿苷转移酶/多(U)聚合酶 PUP-1(又名 CID-1、CDE-1)、PUP-2 和 PUP-3 影响生殖细胞身份、存活和发育。在这里,我们鉴定了这些 PUP 以及第四个预测的多(U)聚合酶 F43E2.1/PUP-4 的小 RNA(sRNA)和 mRNA 靶标。使用遗传和 RNA 测序方法,我们鉴定了每个 PUP 和这些靶标的 U-尾频率和长度。在整个生物体水平上,PUP-1 负责大多数 sRNA 的 U-尾化,而其他 PUP 则有助于修饰离散的 sRNA 子集。此外,PUP-2、PUP-3 的表达,特别是 PUP-4 的表达,限制了某些 sRNAs 的尿嘧啶化。尿嘧啶化状态与 sRNA 丰度之间的关系表明,尿嘧啶化可以根据上下文对丰度产生负面或正面影响。PUP 活性修饰的 sRNAs 主要靶向在整个生物体中表达或在生殖细胞中表达最高的 mRNA。使用 Nanopore 方法获得的 mRNA 数据显示,在没有 PUP-3 的情况下,非腺苷酸化 mRNA 添加 U-尾的情况大大减少。总体而言,这项工作鉴定了 PUP RNA 靶标,定义了尿嘧啶化缺失对 RNA 丰度的影响,并揭示了 PUP 在秀丽隐杆线虫发育中的复杂调控。