Single-molecule visualization of DNA G-quadruplex formation in live cells

被引:283
作者
Di Antonio, Marco [1 ,2 ]
Ponjavic, Aleks [1 ,3 ,4 ]
Radzevicius, Antanas [1 ]
Ranasinghe, Rohan T. [1 ]
Catalano, Marco [1 ]
Zhang, Xiaoyun [1 ]
Shen, Jiazhen [5 ]
Needham, Lisa-Maria [1 ]
Lee, Steven F. [1 ]
Klenerman, David [1 ]
Balasubramanian, Shankar [1 ,5 ,6 ]
机构
[1] Univ Cambridge, Dept Chem, Cambridge, England
[2] Imperial Coll London, Chem Dept, Mol Sci Res Hub, London, England
[3] Univ Leeds, Sch Phys & Astron, Leeds, W Yorkshire, England
[4] Univ Leeds, Sch Food Sci & Nutr, Leeds, W Yorkshire, England
[5] Li Ka Shing Ctr, Cambridge Res Inst, Canc Res UK, Cambridge, England
[6] Univ Cambridge, Sch Clin Med, Cambridge, England
基金
英国工程与自然科学研究理事会; 英国生物技术与生命科学研究理事会; 英国医学研究理事会;
关键词
MICROSCOPY; DYNAMICS;
D O I
10.1038/s41557-020-0506-4
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Substantial evidence now exists to support that formation of DNA G-quadruplexes (G4s) is coupled to altered gene expression. However, approaches that allow us to probe G4s in living cells without perturbing their folding dynamics are required to understand their biological roles in greater detail. Herein, we report a G4-specific fluorescent probe (SiR-PyPDS) that enables single-molecule and real-time detection of individual G4 structures in living cells. Live-cell single-molecule fluorescence imaging of G4s was carried out under conditions that use low concentrations of SiR-PyPDS (20 nM) to provide informative measurements representative of the population of G4s in living cells, without globally perturbing G4 formation and dynamics. Single-molecule fluorescence imaging and time-dependent chemical trapping of unfolded G4s in living cells reveal that G4s fluctuate between folded and unfolded states. We also demonstrate that G4 formation in live cells is cell-cycle-dependent and disrupted by chemical inhibition of transcription and replication. Our observations provide robust evidence in support of dynamic G4 formation in living cells.
引用
收藏
页码:832 / +
页数:20
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