Baldauf A Q, Willwand K, Mumtsidu E, Nüesch J P, Rommelaere J
Department of Applied Tumor Virology, Deutches Krebsforschungszentrum, Heidelberg, Germany.
J Virol. 1997 Feb;71(2):971-80. doi: 10.1128/JVI.71.2.971-980.1997.
We have developed an in vitro system that supports the replication of natural DNA templates of the autonomous parvovirus minute virus of mice (MVM). MVM virion DNA, a single-stranded molecule bracketed by short, terminal, self-complementary sequences, is converted into double-stranded replicative-form (RF) DNA when incubated in mouse A9 fibroblast extract. The 3' end of the newly synthesized complementary strand is ligated to the right-end hairpin of the virion strand, resulting in the formation of a covalently closed RF (cRF) molecule as the major conversion product. cRF DNA is not further replicated in A9 cell extract alone. On addition of purified MVM nonstructural protein NS1 expressed from recombinant baculoviruses or vaccinia viruses, cRF DNA is processed into a right-end (5' end of the virion strand) extended form (5'eRF). This is indicative of NS1-dependent nicking of the right-end hairpin at a distinct position, followed by unfolding of the hairpin and copying of the terminal sequence. In contrast, no resolution of the left-end hairpin can be detected in the presence of NS1. In the course of the right-end nicking reaction, NS1 gets covalently attached to the right-end telomere of the DNA product, as shown by immunoprecipitation with NS1-specific antibodies. The 5'eRF product is the target for additional rounds of NS1-induced nicking and displacement synthesis at the right end, arguing against the requirement of the hairpin structure for recognition of the DNA substrate by NS1. Further processing of the 5'eRF template in vitro leads to the formation of dimeric RF (dRF) DNA in a left-to-left-end configuration, presumably as a result of copying of the whole molecule by displacement synthesis initiated at the right-end telomere. Formation of dRF DNA is highly stimulated by NS1. The experimental results presented in this report support various assumptions of current models of parvovirus DNA replication and provide new insights into the replication functions of the NS1 protein.
我们开发了一种体外系统,该系统可支持小鼠自主细小病毒微小病毒(MVM)天然DNA模板的复制。MVM病毒粒子DNA是一种单链分子,两侧由短的末端自我互补序列包围,当在小鼠A9成纤维细胞提取物中孵育时,会转化为双链复制型(RF)DNA。新合成的互补链的3'末端与病毒粒子链的右端发夹连接,导致形成共价闭合的RF(cRF)分子作为主要的转化产物。cRF DNA不会在单独的A9细胞提取物中进一步复制。添加从重组杆状病毒或痘苗病毒表达的纯化MVM非结构蛋白NS1后,cRF DNA会加工成右端(病毒粒子链的5'末端)延伸形式(5'eRF)。这表明NS1依赖于在一个独特位置对右端发夹进行切口,随后发夹展开并复制末端序列。相比之下,在存在NS1的情况下,未检测到左端发夹的切割。在右端切口反应过程中,如用NS1特异性抗体进行免疫沉淀所示,NS1与DNA产物的右端端粒共价连接。5'eRF产物是NS1诱导的右端额外切口和置换合成轮次的靶标,这表明NS1识别DNA底物不需要发夹结构。体外对5'eRF模板的进一步加工导致形成左到左端构型的二聚体RF(dRF)DNA,推测这是由于从右端端粒起始的置换合成复制了整个分子的结果。dRF DNA的形成受到NS1的高度刺激。本报告中呈现的实验结果支持了细小病毒DNA复制当前模型的各种假设,并为NS1蛋白的复制功能提供了新的见解。