G-quadruplexes on chromosomal DNA negatively regulates topoisomerase 1 activity

被引:5
作者
Liang, Hui-ting [1 ,2 ]
Yan, Jiang-yu [1 ]
Yao, Hao-jun [1 ]
Zhang, Xue-nan [1 ]
Xing, Zhi-ming [1 ]
Liu, Lin [3 ]
Chen, Yao-qing [3 ]
Li, Guo-rui [1 ]
Huang, Jing [1 ]
He, Yi-de [2 ]
Zheng, Ke-wei [1 ]
机构
[1] Hunan Univ, Sch Biomed Sci, Changsha 410082, Peoples R China
[2] Sun Yat Sen Univ, Sch Pharmaceut Sci, Shenzhen Campus, Shenzhen 518107, Peoples R China
[3] Sun Yat Sen Univ, Sch Publ Hlth Shenzhen, Shenzhen Campus, Shenzhen 518107, Peoples R China
基金
中国国家自然科学基金;
关键词
HYBRID G-QUADRUPLEX; TRANSCRIPTION; RELAXATION; INHIBITORS; REVEALS; STRANDS; MOTIFS; CANCER; REGION; SITE;
D O I
10.1093/nar/gkae073
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
Human DNA topoisomerase 1 (Top1) is a crucial enzyme responsible for alleviating torsional stress on DNA during transcription and replication, thereby maintaining genome stability. Previous researches had found that non-working Top1 interacted extensively with chromosomal DNA in human cells. However, the reason for its retention on chromosomal DNA remained unclear. In this study, we discovered a close association between Top1 and chromosomal DNA, specifically linked to the presence of G-quadruplex (G4) structures. G4 structures, formed during transcription, trap Top1 and hinder its ability to relax neighboring DNAs. Disruption of the Top1-G4 interaction using G4 ligand relieved the inhibitory effect of G4 on Top1 activity, resulting in a further reduction of R-loop levels in cells. Additionally, the activation of Top1 through the use of a G4 ligand enhanced the toxicity of Top1 inhibitors towards cancer cells. Our study uncovers a negative regulation mechanism of human Top1 and highlights a novel pathway for activating Top1. Graphical Abstract
引用
收藏
页码:2142 / 2156
页数:15
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