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Topology of a DNA G-Quadruplex Structure Formed in the HIV-1 Promoter: A Potential Target for Anti-HIV Drug Development
被引:127
|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.
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页码:5249 / 5252
页数:4
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