School of Biomedical Sciences, Hunan University, Changsha 410082, China.
School of Pharmaceutical Sciences, Shenzhen Campus of Sun Yat-Sen University, Shenzhen 518107, China.
Nucleic Acids Res. 2024 Mar 21;52(5):2142-2156. doi: 10.1093/nar/gkae073.
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.
人类 DNA 拓扑异构酶 1(Top1)是一种关键的酶,负责在转录和复制过程中缓解 DNA 的扭转应力,从而维持基因组的稳定性。先前的研究发现,非工作状态的 Top1 与人细胞中的染色体 DNA 广泛相互作用。然而,其在染色体 DNA 上保留的原因尚不清楚。在这项研究中,我们发现 Top1 与染色体 DNA 密切相关,特别是与 G-四链体(G4)结构的存在有关。在转录过程中形成的 G4 结构会捕获 Top1 并阻碍其松弛邻近 DNA 的能力。使用 G4 配体破坏 Top1-G4 相互作用,会减轻 G4 对 Top1 活性的抑制作用,从而导致细胞中 R 环水平进一步降低。此外,通过使用 G4 配体激活 Top1 会增强 Top1 抑制剂对癌细胞的毒性。我们的研究揭示了人类 Top1 的负调控机制,并强调了激活 Top1 的新途径。