Instituto de Biología Molecular y Celular de Rosario (IBR), Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Universidad Nacional de Rosario (UNR), Ocampo y Esmeralda, Rosario S200EZP, Santa Fe, Argentina.
Plataforma Argentina de Biología Estructural y Metabolómica (PLABEM), Ocampo y Esmeralda, Rosario S200EZP, Santa Fe, Argentina.
Int J Mol Sci. 2021 Mar 5;22(5):2614. doi: 10.3390/ijms22052614.
The Coronavirus Disease 2019 (COVID-19) pandemic has become a global health emergency with no effective medical treatment and with incipient vaccines. It is caused by a new positive-sense RNA virus called severe acute respiratory syndrome-related coronavirus 2 (SARS-CoV-2). G-quadruplexes (G4s) are nucleic acid secondary structures involved in the control of a variety of biological processes including viral replication. Using several G4 prediction tools, we identified highly putative G4 sequences (PQSs) within the positive-sense (+gRNA) and negative-sense (-gRNA) RNA strands of SARS-CoV-2 conserved in related betacoronaviruses. By using multiple biophysical techniques, we confirmed the formation of two G4s in the +gRNA and provide the first evidence of G4 formation by two PQSs in the -gRNA of SARS-CoV-2. Finally, biophysical and molecular approaches were used to demonstrate for the first time that CNBP, the main human cellular protein bound to SARS-CoV-2 RNA genome, binds and promotes the unfolding of G4s formed by both strands of SARS-CoV-2 RNA genome. Our results suggest that G4s found in SARS-CoV-2 RNA genome and its negative-sense replicative intermediates, as well as the cellular proteins that interact with them, are relevant factors for viral genes expression and replication cycle, and may constitute interesting targets for antiviral drugs development.
新型冠状病毒病 2019(COVID-19)大流行已成为全球卫生紧急事件,目前尚无有效的治疗方法,也只有初步研发的疫苗。该疾病由一种新型正链 RNA 病毒引起,称为严重急性呼吸系统综合征相关冠状病毒 2(SARS-CoV-2)。四链体(G4s)是参与控制多种生物过程的核酸二级结构,包括病毒复制。使用几种 G4 预测工具,我们在 SARS-CoV-2 的正链(+gRNA)和负链(-gRNA)RNA 链中鉴定出高度可能的 G4 序列(PQSs),这些序列在相关的β冠状病毒中保守。通过使用多种生物物理技术,我们证实了在+gRNA 中形成了两个 G4,并且首次提供了 SARS-CoV-2 的-gRNA 中两个 PQS 形成 G4 的证据。最后,生物物理和分子方法首次被用于证明,CNBP 是与 SARS-CoV-2 RNA 基因组结合的主要人类细胞蛋白,可结合并促进 SARS-CoV-2 RNA 基因组两条链形成的 G4 解折叠。我们的研究结果表明,在 SARS-CoV-2 RNA 基因组及其负链复制中间体中发现的 G4 以及与它们相互作用的细胞蛋白是病毒基因表达和复制周期的重要因素,并且可能成为开发抗病毒药物的有趣靶标。