Butovskaya Elena, Heddi Brahim, Bakalar Blaž, Richter Sara N, Phan Anh Tuân
School of Physical and Mathematical Sciences , Nanyang Technological University , Singapore 637371 , Singapore.
Department of Molecular Medicine , University of Padua , Padua 35121 , Italy.
J Am Chem Soc. 2018 Oct 24;140(42):13654-13662. doi: 10.1021/jacs.8b05332. Epub 2018 Oct 9.
Nucleic acids can form noncanonical four-stranded structures called G-quadruplexes. G-quadruplex-forming sequences are found in several genomes including human and viruses. Previous studies showed that the G-rich sequence located in the U3 promoter region of the HIV-1 long terminal repeat (LTR) folds into a set of dynamically interchangeable G-quadruplex structures. G-quadruplexes formed in the LTR could act as silencer elements to regulate viral transcription. Stabilization of LTR G-quadruplexes by G-quadruplex-specific ligands resulted in decreased viral production, suggesting the possibility of targeting viral G-quadruplex structures for antiviral purposes. Among all the G-quadruplexes formed in the LTR sequence, LTR-III was shown to be the major G-quadruplex conformation in vitro. Here we report the NMR structure of LTR-III in K solution, revealing the formation of a unique quadruplex-duplex hybrid consisting of a three-layer (3 + 1) G-quadruplex scaffold, a 12-nt diagonal loop containing a conserved duplex-stem, a 3-nt lateral loop, a 1-nt propeller loop, and a V-shaped loop. Our structure showed several distinct features including a quadruplex-duplex junction, representing an attractive motif for drug targeting. The structure solved in this study may be used as a promising target to selectively impair the viral cycle.
核酸可以形成称为G-四链体的非经典四链结构。在包括人类和病毒在内的多个基因组中都发现了形成G-四链体的序列。先前的研究表明,位于HIV-1长末端重复序列(LTR)的U3启动子区域的富含G的序列可折叠成一组动态可互换的G-四链体结构。在LTR中形成的G-四链体可以作为沉默元件来调节病毒转录。通过G-四链体特异性配体稳定LTR G-四链体导致病毒产生减少,这表明靶向病毒G-四链体结构用于抗病毒目的的可能性。在LTR序列中形成的所有G-四链体中,LTR-III在体外被证明是主要的G-四链体构象。在这里,我们报告了LTR-III在K溶液中的NMR结构,揭示了一种独特的四链体-双链体杂合体的形成,该杂合体由一个三层(3 + 1)G-四链体支架、一个包含保守双链茎的12个核苷酸的对角环、一个3个核苷酸的侧环、一个1个核苷酸的螺旋桨环和一个V形环组成。我们的结构显示了几个不同的特征,包括一个四链体-双链体连接,这是一个有吸引力的药物靶向基序。本研究中解析的结构可能作为一个有前景的靶点来选择性地破坏病毒周期。