Liew Shiau Wei, Cao Dong, Petersen Riley J, Butcher Samuel E, Kennedy Scott G, Kwok Chun Kit
Department of Chemistry and State Key Laboratory of Marine Pollution, City University of Hong Kong, Kowloon Tong, Hong Kong SAR, 999077, China.
Department of Genetics, Blavatnik Institute at Harvard Medical School, Boston, MA 02115, United States.
Nucleic Acids Res. 2025 Feb 27;53(5). doi: 10.1093/nar/gkaf137.
G-quadruplex (G4) is a guanine-rich secondary structure found in DNA and RNA involved in various biological roles. Recently, a non-canonical RNA G-quadruplex (rG4), known as poly(UG) (pUG) fold, was discovered in Caenorhabditis elegans. This unique structure was found to induce RNA interference (RNAi) upon recruitment of RNA-dependent RNA polymerase (RdRP), resulting in trans-generational gene silencing. Herein, we develop a novel L-RNA aptamer, L-apt3.1, that binds to the pUG fold. We uncover that L-apt3.1 consists of a parallel rG4 structural motif, and mutagenesis analysis illustrates that the rG4 motif in L-apt3.1 is essential for pUG fold recognition. We show that L-apt3.1 interacts strongly with pUG fold, and notably, it is the first reported aptamer that can bind to pUG fold in vitro. We also demonstrate that L-apt3.1 possesses great biostability in cellular environments and negligible toxicity in vivo. Furthermore, we report that L-apt3.1 can interact with pUG fold in vivo, and with a comparable performance to the G4 ligand, N-methyl mesoporphyrin, in inhibiting gene silencing in C. elegans. Overall, we demonstrate the development of pUG fold-targeting L-RNA aptamer for the first time, and show that this new aptamer tool can be applied to control pUG fold-mediated gene expression in vivo.
G-四链体(G4)是一种富含鸟嘌呤的二级结构,存在于DNA和RNA中,参与多种生物学功能。最近,在线虫中发现了一种非规范的RNA G-四链体(rG4),即聚(UG)(pUG)折叠结构。发现这种独特结构在招募RNA依赖性RNA聚合酶(RdRP)后会诱导RNA干扰(RNAi),从而导致跨代基因沉默。在此,我们开发了一种新型的L-RNA适配体L-apt3.1,它能与pUG折叠结构结合。我们发现L-apt3.1由一个平行的rG4结构基序组成,诱变分析表明L-apt3.1中的rG4基序对于识别pUG折叠结构至关重要。我们表明L-apt3.1与pUG折叠结构有强烈的相互作用,值得注意的是,它是第一个报道的能在体外结合pUG折叠结构的适配体。我们还证明L-apt3.1在细胞环境中具有很高的生物稳定性,在体内的毒性可忽略不计。此外,我们报告L-apt3.1能在体内与pUG折叠结构相互作用,并且在抑制线虫基因沉默方面,其性能与G4配体N-甲基中卟啉相当。总体而言,我们首次展示了针对pUG折叠结构的L-RNA适配体的开发,并表明这种新的适配体工具可用于在体内控制pUG折叠结构介导的基因表达。