Major G-Quadruplex Form of HIV-1 LTR Reveals a (3+1) Folding Topology Containing a Stem-Loop

被引:81
|
作者
Butovskaya, Elena [1 ,2 ]
Heddi, Brahim [1 ,3 ]
Bakalar, Blaz [1 ]
Richter, Sara N. [2 ]
Anh Tuan Phan [1 ]
机构
[1] Nanyang Technol Univ, Sch Phys & Math Sci, Singapore 637371, Singapore
[2] Univ Padua, Dept Mol Med, I-35121 Padua, Italy
[3] Ecole Normale Super Paris Saclay, CNRS, Lab Biol & Pharmacol Appl, F-94235 Cachan, France
基金
欧洲研究理事会; 新加坡国家研究基金会;
关键词
LONG TERMINAL REPEAT; STRUCTURAL BASIS; MESSENGER-RNA; NMR STRUCTURE; DNA; PROMOTER; LIGAND; TRANSCRIPTION; BINDING; GENOME;
D O I
10.1021/jacs.8b05332
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
引用
收藏
页码:13654 / 13662
页数:9
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