Department of Molecular Medicine, University of Padua, via Gabelli 63, 35121, Padua, Italy.
Sci Rep. 2017 May 17;7(1):2018. doi: 10.1038/s41598-017-02291-1.
G-quadruplexes (G4s) are secondary structures of nucleic acids that epigenetically regulate cellular processes. In the human immunodeficiency lentivirus 1 (HIV-1), dynamic G4s are located in the unique viral LTR promoter. Folding of HIV-1 LTR G4s inhibits viral transcription; stabilization by G4 ligands intensifies this effect. Cellular proteins modulate viral transcription by inducing/unfolding LTR G4s. We here expanded our investigation on the presence of LTR G4s to all lentiviruses. G4s in the 5'-LTR U3 region were completely conserved in primate lentiviruses. A G4 was also present in a cattle-infecting lentivirus. All other non-primate lentiviruses displayed hints of less stable G4s. In primate lentiviruses, the possibility to fold into G4s was highly conserved among strains. LTR G4 sequences were very similar among phylogenetically related primate viruses, while they increasingly differed in viruses that diverged early from a common ancestor. A strong correlation between primate lentivirus LTR G4s and Sp1/NFκB binding sites was found. All LTR G4s folded: their complexity was assessed by polymerase stop assay. Our data support a role of the lentiviruses 5'-LTR G4 region as control centre of viral transcription, where folding/unfolding of G4s and multiple recruitment of factors based on both sequence and structure may take place.
G-四链体(G4s)是核酸的二级结构,通过表观遗传调控细胞过程。在人类免疫缺陷病毒 1(HIV-1)中,动态 G4s 位于独特的病毒长末端重复(LTR)启动子中。HIV-1 LTR G4s 的折叠抑制病毒转录;G4 配体的稳定增强了这种效应。细胞蛋白通过诱导/展开 LTR G4s 来调节病毒转录。我们在此将对 LTR G4s 的存在的研究扩展到所有慢病毒。灵长类慢病毒 5'-LTR U3 区域的 G4s 完全保守。牛感染的慢病毒中也存在 G4。所有其他非灵长类慢病毒显示出不太稳定的 G4s 的迹象。在灵长类慢病毒中,不同毒株之间形成 G4s 的可能性高度保守。LTR G4 序列在系统发育相关的灵长类病毒中非常相似,而在与共同祖先早期分化的病毒中则越来越不同。发现灵长类慢病毒 LTR G4s 与 Sp1/NFκB 结合位点之间存在很强的相关性。所有 LTR G4s 都能折叠:通过聚合酶停止试验评估其复杂性。我们的数据支持慢病毒 5'-LTR G4 区域作为病毒转录的控制中心的作用,在这个区域,G4s 的折叠/展开以及基于序列和结构的多种因子募集可能发生。