Molecular Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY, United States.
Molecular Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY, United States.
Methods Enzymol. 2022;672:233-260. doi: 10.1016/bs.mie.2022.02.020. Epub 2022 Mar 25.
G-quadruplexes (G4s) are non-canonical nucleic acid structures that form in G-rich regions of the genome and threaten genome stability by interfering with DNA replication. However, the underlying mechanisms are poorly understood. We have recently found that G4s can stall eukaryotic replication forks by blocking the progression of replicative DNA helicase, CMG. In this paper, we detail the methodology of DNA unwinding assays to investigate the impact of G4s on CMG progression. The method details the purification of recombinantly expressed CMG from the budding yeast, Saccharomyces cerevisiae, purification of synthetic oligonucleotides, and covers various aspects of DNA substrate preparation, reaction setup and result interpretation. The use of synthetic oligonucleotides provides the advantage of allowing to control the formation of G4 structures in DNA substrates. The methods discussed here can be adapted for the study of other DNA helicases and provide a general template for the assembly of DNA substrates with distinct G4 structures.
四链体(G4s)是形成于基因组中富含鸟嘌呤(G)区域的非经典核酸结构,通过干扰 DNA 复制来威胁基因组稳定性。然而,其潜在机制尚不清楚。我们最近发现,G4s 可以通过阻止复制性 DNA 解旋酶 CMG 的前进来阻止真核复制叉。在本文中,我们详细介绍了 DNA 解旋测定的方法,以研究 G4s 对 CMG 前进的影响。该方法详述了从芽殖酵母酿酒酵母中重组表达的 CMG 的纯化、合成寡核苷酸的纯化以及涵盖了 DNA 底物制备、反应设置和结果解释的各个方面。使用合成寡核苷酸提供了控制 DNA 底物中 G4 结构形成的优势。这里讨论的方法可以适应其他 DNA 解旋酶的研究,并为具有不同 G4 结构的 DNA 底物的组装提供通用模板。