Department of Molecular Medicine, University of Padua, Padua, Italy.
PLoS One. 2013 Aug 27;8(8):e73121. doi: 10.1371/journal.pone.0073121. eCollection 2013.
G-quadruplexes are tetraplex structures of nucleic acids that can form in G-rich sequences. Their presence and functional role have been established in telomeres, oncogene promoters and coding regions of the human chromosome. In particular, they have been proposed to be directly involved in gene regulation at the level of transcription. Because the HIV-1 Nef protein is a fundamental factor for efficient viral replication, infectivity and pathogenesis in vitro and in vivo, we investigated G-quadruplex formation in the HIV-1 nef gene to assess the potential for viral inhibition through G-quadruplex stabilization. A comprehensive computational analysis of the nef coding region of available strains showed the presence of three conserved sequences that were uniquely clustered. Biophysical testing proved that G-quadruplex conformations were efficiently stabilized or induced by G-quadruplex ligands in all three sequences. Upon incubation with a G-quadruplex ligand, Nef expression was reduced in a reporter gene assay and Nef-dependent enhancement of HIV-1 infectivity was significantly repressed in an antiviral assay. These data constitute the first evidence of the possibility to regulate HIV-1 gene expression and infectivity through G-quadruplex targeting and therefore open a new avenue for viral treatment.
四链体是富含鸟嘌呤的核酸形成的四链结构。它们在端粒、癌基因启动子和人类染色体编码区的存在及其功能作用已经得到确立。特别是,它们被提议直接参与转录水平的基因调控。由于 HIV-1 Nef 蛋白是病毒在体外和体内高效复制、感染和发病的基本因素,我们研究了 HIV-1 nef 基因中的四链体形成,以评估通过四链体稳定化抑制病毒的潜力。对现有毒株 nef 编码区的全面计算分析表明,存在三个独特聚集的保守序列。生物物理测试证明,在所有三个序列中,G-四链体配体能够有效地稳定或诱导 G-四链体构象。在用 G-四链体配体孵育后,在报告基因测定中观察到 Nef 表达减少,在抗病毒测定中,Nef 依赖性 HIV-1 感染性增强被显著抑制。这些数据首次证明了通过靶向 G-四链体调节 HIV-1 基因表达和感染性的可能性,因此为病毒治疗开辟了新途径。