Department of Molecular Biology and Genetics, Aarhus University, 8000 Aarhus C, Denmark.
Department of Clinical Medicine, Aarhus University, 8000 Aarhus C, Denmark.
Nucleic Acids Res. 2022 Jun 24;50(11):6332-6342. doi: 10.1093/nar/gkac482.
We have investigated the function of human topoisomerase 1 (TOP1) in regulation of G-quadruplex (G4) formation in the Pu27 region of the MYC P1 promoter. Pu27 is among the best characterized G4 forming sequences in the human genome and it is well known that promoter activity is inhibited upon G4 formation in this region. We found that TOP1 downregulation stimulated transcription from a promoter with wildtype Pu27 but not if the G4 motif in Pu27 was interrupted by mutation(s). The effect was not specific to the MYC promoter and similar results were obtained for the G4 forming promoter element WT21. The other major DNA topoisomerases with relaxation activity, topoisomerases 2α and β, on the other hand, did not affect G4 dependent promoter activity. The cellular studies were supported by in vitro investigations demonstrating a high affinity of TOP1 for wildtype Pu27 but not for mutant sequences unable to form G4. Moreover, TOP1 was able to induce G4 formation in Pu27 inserted in double stranded plasmid DNA in vitro. This is the first time TOP1 has been demonstrated capable of inducing G4 formation in double stranded DNA and of influencing G4 formation in cells.
我们研究了人类拓扑异构酶 1(TOP1)在调节 MYC P1 启动子 Pu27 区域内 G-四链体(G4)形成中的功能。Pu27 是人类基因组中研究得最好的 G4 形成序列之一,众所周知,该区域的 G4 形成会抑制启动子活性。我们发现 TOP1 的下调会刺激野生型 Pu27 启动子的转录,但如果 Pu27 中的 G4 模体发生突变则不会。这种效应不是 MYC 启动子所特有的,对于 G4 形成启动元件 WT21 也得到了类似的结果。另一方面,具有松弛活性的其他主要 DNA 拓扑异构酶,拓扑异构酶 2α 和 2β,不会影响 G4 依赖的启动子活性。细胞研究得到了体外研究的支持,证明 TOP1 与野生型 Pu27 具有高亲和力,但与不能形成 G4 的突变序列没有亲和力。此外,TOP1 能够在体外诱导插入双链质粒 DNA 中的 Pu27 形成 G4。这是首次证明 TOP1 能够在双链 DNA 中诱导 G4 形成,并影响细胞中的 G4 形成。