A pyridyl carboxamide molecule selectively stabilizes DNA G-quadruplex and regulates duplex-quadruplex competition

被引:8
|
作者
Xu, Liang [1 ]
Wu, Weixin [1 ]
Ding, Jie [1 ]
Feng, Shuo [1 ]
Xing, Xiwen [1 ]
Deng, Minggang [1 ]
Zhou, Xiang [1 ,2 ]
机构
[1] Wuhan Univ, State Key Lab Virol, Key Lab Biomed Polymers, Coll Chem & Mol Sci,Minist Educ, Wuhan 430072, Hubei, Peoples R China
[2] Shanghai Inst Organ Chem, State Key Lab Bioorgan & Nat Prod Chem, Shanghai, Peoples R China
来源
RSC ADVANCES | 2012年 / 2卷 / 03期
关键词
PROXIMAL PROMOTER REGION; TELOMERASE INHIBITOR; LIGANDS; TRANSCRIPTION; RECOGNITION; ONCOGENE; SQUARE; TARGET; GENE;
D O I
10.1039/c1ra00851j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
G-Quadruplexes formed by G-rich DNA are of broad interest due to their involvement in telomere function, gene transcription and recombination. Small ligands that interact strongly with G-quadruplexes have been considered to further influence telomeric function and gene transcription. Because most G-rich sequences are trapped in duplex structures in gene promoters, ligands that can stabilize G-quadruplexes in the presence of their complimentary strands would likely have strong effects on gene transcription. Here, we report a novel simple small molecule (pyridyl carboxamide), consisting of three pyridine rings and four amide bonds. Comparing with some reported G-quadruplex ligands, this molecule not only selectively stabilizes G-quadruplexes rather than duplexes, but also maintains a G-quadruplex structure even if the G-rich region was trapped in long double-stranded DNA (dsDNA). It is widely believed that the dissociation of duplexes is involved in gene transcription and that the formation of the G-quadruplex influences some oncogene expression. Py-Am exhibited strong G-quadruplex-forming ability within a long dsDNA sequence, suggesting it would have potent effects on the G-quadruplex-forming sequences involved in gene transcription.
引用
收藏
页码:894 / 899
页数:6
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