Topology of a DNA G-Quadruplex Structure Formed in the HIV-1 Promoter: A Potential Target for Anti-HIV Drug Development

被引:126
|
作者
Amrane, Samir [1 ,2 ]
Kerkour, Abdelaziz [1 ,2 ]
Bedrat, Amina [1 ,2 ]
Vialet, Brune [1 ,2 ]
Andreola, Marie-Line [1 ,3 ]
Mergny, Jean-Louis [1 ,2 ]
机构
[1] Univ Bordeaux, F-33000 Bordeaux, France
[2] INSERM, U869, IECB, ARNA Lab, F-33600 Pessac, France
[3] CNRS, UMR 5234, F-33076 Bordeaux, France
关键词
INTRAMOLECULAR G-QUADRUPLEX; ADOPTS; GENOME;
D O I
10.1021/ja501500c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Nucleic acid sequences containing guanine tracts are able to adopt noncanonical four-stranded nucleic acid structures called G-quadruplexes (G4s). These structures are based on the stacking of two or more G-tetrads; each tetrad is a planar association of four guanines held together by eight hydrogen bonds. In this study, we analyzed a conserved G-rich region from HIV-1 promoter that is known to regulate the transcription of the HIV-1 provirus. Strikingly, our analysis of an alignment of 1684 HIV-1 sequences from this region showed a high conservation of the ability to form G4 structures despite a lower conservation of the nucleotide primary sequence. Using NMR spectroscopy, we determined the G4 topology adopted by a DNA sequence from this region (HIV-PRO1: 5' TGGCCTGGGCGGGACTGGG 3'). This DNA fragment formed a stable two G-tetrad antiparallel G4 with an additional Watson-Crick CG base pair. This hybrid structure may be critical for HIV-1 gene expression and is potentially a novel target for anti-HIV-1 drug development.
引用
收藏
页码:5249 / 5252
页数:4
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