Ward P, Urcelay E, Kotin R, Safer B, Berns K I
Department of Microbiology, Hearst Microbiology Research Center, Cornell University Medical College, New York, New York 10021.
J Virol. 1994 Sep;68(9):6029-37. doi: 10.1128/JVI.68.9.6029-6037.1994.
The adeno-associated virus (AAV) nonstructural protein Rep 68 is required for viral DNA replication. An in vitro assay has been developed in which addition of Rep 68 to an extract from uninfected HeLa cells supports AAV DNA replication. In this paper, we report characterization of the replication process when a fusion of the maltose binding protein and Rep 68, expressed in Escherichia coli, was used in the assay. Replication was observed when the template was either linear double-stranded AAV DNA or a plasmid construct containing intact AAV DNA. When the recombinant plasmid construct was used as the template, there was replication of pBR322 DNA as well as the AAV DNA; however, linear pBR322 DNA was not replicated. When the plasmid construct was the template, replication appeared to initiate on the intact plasmid and led to separation of the AAV sequences from those of the vector, a process which has been termed rescue. There was no evidence that replication could initiate on the products of rescue. Rep 68 can make a site-specific nick 124 nucleotides from the 3' end of AAV DNA; the site of the nick has been called the terminal resolution site. Our data are most consistent with initiation occurring at the terminal resolution site and proceeding toward the 3' terminus. When the template was the plasmid construct, either elongation continued past the junction into pBR322 sequences or the newly synthesized sequence hairpinned, switched template strands, and replicated the AAV DNA. Replication was linear for 4 h, during which time 70% of the maximal synthesis took place. An additional finding was that the Rep fusion could resolve AAV dimer length duplex intermediates into monomer duplexes without DNA synthesis.
腺相关病毒(AAV)的非结构蛋白Rep 68是病毒DNA复制所必需的。已经开发了一种体外测定方法,其中将Rep 68添加到未感染的HeLa细胞提取物中可支持AAV DNA复制。在本文中,我们报告了在该测定中使用在大肠杆菌中表达的麦芽糖结合蛋白与Rep 68的融合体时复制过程的特征。当模板为线性双链AAV DNA或含有完整AAV DNA的质粒构建体时,观察到复制。当使用重组质粒构建体作为模板时,pBR322 DNA以及AAV DNA都会复制;然而,线性pBR322 DNA不会复制。当质粒构建体为模板时,复制似乎在完整质粒上起始,并导致AAV序列与载体序列分离,这一过程被称为拯救。没有证据表明复制可以在拯救产物上起始。Rep 68可以在距AAV DNA 3'末端124个核苷酸处产生位点特异性切口;该切口位点被称为末端分辨率位点。我们的数据最符合在末端分辨率位点起始并向3'末端进行的情况。当模板为质粒构建体时,要么延伸越过连接处进入pBR322序列,要么新合成的序列形成发夹结构,切换模板链,并复制AAV DNA。复制在4小时内呈线性,在此期间发生了最大合成量的70%。另一个发现是,Rep融合体可以在不进行DNA合成的情况下将AAV二聚体长双链中间体分解为单体双链体。