Colletti Kelly S, Smallenburg Kate E, Xu Yiyang, Pari Gregory S
University of Nevada--Reno, Department of Microbiology, School of Medicine, Howard Bldg., Reno, NV 89557, USA.
J Virol. 2007 Jul;81(13):7077-85. doi: 10.1128/JVI.00058-07. Epub 2007 Apr 25.
Human cytomegalovirus (HCMV) lytic DNA replication is initiated at the complex cis-acting oriLyt region, which spans nearly 3 kb. DNA synthesis requires six core proteins together with UL84 and IE2. Previously, two essential regions were identified within oriLyt. Essential region I (nucleotides [nt] 92209 to 92573) can be replaced with the constitutively active simian virus 40 promoter, which in turn eliminates the requirement for IE2 in the origin-dependent transient-replication assay. Essential region II (nt 92979 to 93513) contains two elements of interest: an RNA/DNA hybrid domain and an inverted repeat sequence capable of forming a stem-loop structure. Our studies now reveal for the first time that UL84 interacts with a stem-loop RNA oligonucleotide in vitro, and although UL84 interacted with other nucleic acid substrates, a specific interaction occurred only with the RNA stem-loop. Increasing concentrations of purified UL84 produced a remarkable downward-staircase pattern, which is not due to a nuclease activity but is dependent upon the presence of secondary structures, suggesting that UL84 modifies the conformation of the RNA substrate. Cross-linking experiments show that UL84 possibly changes the conformation of the RNA substrate. The addition of purified IE2 to the in vitro binding reaction did not affect binding to the stem-loop structure. Chromatin immunoprecipitation assays performed using infected cells and purified virus show that UL84 is bound to oriLyt in a region adjacent to the RNA/DNA hybrid and the stem-loop structure. These results solidify UL84 as the potential initiator of HCMV DNA replication through a unique interaction with a conserved RNA stem-loop structure within oriLyt.
人巨细胞病毒(HCMV)的裂解性DNA复制起始于复杂的顺式作用oriLyt区域,该区域跨度近3 kb。DNA合成需要六种核心蛋白以及UL84和IE2。此前,在oriLyt内鉴定出两个必需区域。必需区域I(核苷酸[nt] 92209至92573)可被组成型活性猿猴病毒40启动子取代,这反过来消除了在依赖于起始点的瞬时复制试验中对IE2的需求。必需区域II(nt 92979至93513)包含两个感兴趣的元件:一个RNA/DNA杂交结构域和一个能够形成茎环结构的反向重复序列。我们的研究首次揭示,UL84在体外与茎环RNA寡核苷酸相互作用,尽管UL84与其他核酸底物相互作用,但仅与RNA茎环发生特异性相互作用。纯化的UL84浓度增加产生了显著的向下阶梯模式,这不是由于核酸酶活性,而是取决于二级结构的存在,表明UL84改变了RNA底物的构象。交联实验表明,UL84可能改变了RNA底物的构象。在体外结合反应中加入纯化的IE2并不影响与茎环结构的结合。使用感染细胞和纯化病毒进行的染色质免疫沉淀试验表明,UL84在与RNA/DNA杂交区域和茎环结构相邻的区域与oriLyt结合。这些结果通过与oriLyt内保守的RNA茎环结构的独特相互作用,巩固了UL84作为HCMV DNA复制潜在起始因子的地位。