Department of Microbiology, Sungkyunkwan University School of Medicine, Suwon, Republic of Korea.
Department of Biology, Stanford University, Stanford, CA, USA.
Nat Commun. 2024 Aug 27;15(1):7353. doi: 10.1038/s41467-024-51797-6.
G-quadruplex (G4) structures are found in eukaryotic cell replication origins, but their role in origin function remains unclear. In this study G4 motifs are found in the lytic DNA replication origin (oriLyt) of human cytomegalovirus (HCMV) and recombinant viruses show that a G4 motif in oriLyt essential region I (ER-I) is necessary for viral growth. Replication assays of oriLyt-containing plasmids and biochemical/biophysical analyses show that G4 formation in ER-I is crucial for viral DNA replication. G4 pull-down analysis identifies viral DNA replication factors, such as IE2, UL84, and UL44, as G4-binding proteins. In enzyme-linked immunosorbent assays, specific G4-binding ligands inhibit G4 binding by the viral proteins. The Epstein-Barr virus oriLyt core element also forms a stable G4 that could substitute for the oriLyt ER-I G4 in HCMV. These results demonstrate that viral G4s in replication origins represent an essential structural element in recruiting replication factors and might be a therapeutic target against viral infections.
四链体(G4)结构存在于真核细胞复制起点中,但它们在复制起点功能中的作用仍不清楚。本研究发现人巨细胞病毒(HCMV)的裂解型 DNA 复制起点(oriLyt)中存在 G4 基序,重组病毒表明 oriLyt 必需区 I(ER-I)中的 G4 基序对于病毒生长是必需的。含有 oriLyt 的质粒的复制测定和生化/生物物理分析表明,ER-I 中的 G4 形成对于病毒 DNA 复制至关重要。G4 下拉分析鉴定出病毒 DNA 复制因子,如 IE2、UL84 和 UL44,作为 G4 结合蛋白。在酶联免疫吸附测定中,特异性 G4 结合配体抑制病毒蛋白与 G4 的结合。EB 病毒 oriLyt 核心元件也形成稳定的 G4,可以替代 HCMV 中 oriLyt ER-I G4。这些结果表明,复制起点中的病毒 G4 代表招募复制因子的必需结构元件,可能成为抗病毒感染的治疗靶点。