Structure and possible function of a G-quadruplex in the long terminal repeat of the proviral HIV-1 genome

被引:66
|
作者
De Nicola, Beatrice [1 ,2 ]
Lech, Christopher J. [1 ]
Heddi, Brahim [1 ]
Regmi, Sagar [1 ]
Frasson, Ilaria [2 ]
Perrone, Rosalba [2 ]
Richter, Sara N. [2 ]
Anh Tuan Phan [1 ]
机构
[1] Nanyang Technol Univ, Sch Math & Phys Sci, Singapore, Singapore
[2] Univ Padua, Dept Mol Med, I-35100 Padua, Italy
基金
欧洲研究理事会;
关键词
AMYOTROPHIC-LATERAL-SCLEROSIS; NUCLEIC-ACIDS; LTR PROMOTER; DNA; RNA; CELLS; TRANSCRIPTION; SEQUENCES; TOPOLOGY; REGION;
D O I
10.1093/nar/gkw432
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The long terminal repeat (LTR) of the proviral human immunodeficiency virus (HIV)-1 genome is integral to virus transcription and host cell infection. The guanine-rich U3 region within the LTR promoter, previously shown to form G-quadruplex structures, represents an attractive target to inhibit HIV transcription and replication. In this work, we report the structure of a biologically relevant G-quadruplex within the LTR promoter region of HIV-1. The guanine-rich sequence designated LTR-IV forms a well-defined structure in physiological cationic solution. The nuclear magnetic resonance (NMR) structure of this sequence reveals a parallel-stranded G-quadruplex containing a single-nucleotide thymine bulge, which participates in a conserved stacking interaction with a neighboring single-nucleotide adenine loop. Transcription analysis in a HIV-1 replication competent cell indicates that the LTR-IV region may act as a modulator of G-quadruplex formation in the LTR promoter. Consequently, the LTR-IV G-quadruplex structure presented within this work could represent a valuable target for the design of HIV therapeutics.
引用
收藏
页码:6442 / 6451
页数:10
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