Leiden Institute of Chemistry, Leiden University, Einsteinweg 55, 2333CC, Leiden, The Netherlands.
Sci Rep. 2023 Sep 25;13(1):15987. doi: 10.1038/s41598-023-43001-4.
RNAs that are able to prevent degradation by the 5'-3' exoribonuclease Xrn1 have emerged as crucial structures during infection by an increasing number of RNA viruses. Several plant viruses employ the so-called coremin motif, an Xrn1-resistant RNA that is usually located in 3' untranslated regions. Investigation of its structural and sequence requirements has led to its identification in plant virus families beyond those in which the coremin motif was initially discovered. In this study, we identified coremin-like motifs that deviate from the original in the number of nucleotides present in the loop region of the 5' proximal hairpin. They are present in a number of viral families that previously did not have an Xrn1-resistant RNA identified yet, including the double-stranded RNA virus families Hypoviridae and Chrysoviridae. Through systematic mutational analysis, we demonstrated that a coremin motif carrying a 6-nucleotide loop in the 5' proximal hairpin generally requires a YGNNAD consensus for stalling Xrn1, similar to the previously determined YGAD consensus required for Xrn1 resistance of the original coremin motif. Furthermore, we determined the minimal requirements for the 3' proximal hairpin. Since some putative coremin motifs were found in intergenic regions or coding sequences, we demonstrated their capacity for inhibiting translation through an in vitro ribosomal scanning inhibition assay. Consequently, this study provides a further expansion on the number of viral families with known Xrn1-resistant elements, while adding a novel, potentially regulatory function for this structure.
在越来越多的 RNA 病毒感染过程中,能够防止 5' - 3' 外切核糖核酸酶 Xrn1 降解的 RNA 已成为关键结构。几种植物病毒采用所谓的核心基序,这是一种对 Xrn1 有抗性的 RNA,通常位于 3' 非翻译区。对其结构和序列要求的研究导致了其在最初发现核心基序的植物病毒家族之外的植物病毒家族中的鉴定。在这项研究中,我们鉴定了核心基序类似物,它们在 5' 近端发夹环区的核苷酸数量上与原始核心基序有所不同。它们存在于一些先前没有鉴定出对 Xrn1 有抗性 RNA 的病毒家族中,包括双链 RNA 病毒科 Hypoviridae 和 Chrysoviridae。通过系统的突变分析,我们证明了携带 5' 近端发夹环中 6 个核苷酸环的核心基序通常需要 YGNNAD 共识来阻止 Xrn1,类似于先前确定的 YGAD 共识,该共识需要原始核心基序对 Xrn1 抗性。此外,我们确定了 3' 近端发夹的最小要求。由于在基因间区或编码序列中发现了一些假定的核心基序,我们通过体外核糖体扫描抑制测定证明了它们抑制翻译的能力。因此,这项研究进一步扩大了已知具有 Xrn1 抗性元件的病毒家族的数量,并为该结构增加了一种新的、潜在的调节功能。