Senapathy P, Tratschin J D, Carter B J
J Mol Biol. 1984 Oct 15;179(1):1-20. doi: 10.1016/0022-2836(84)90303-6.
When the entire adeno-associated virus (AAV) genome is inserted into a bacterial plasmid, infectious AAV genomes can be rescued and replicated when the recombinant AAV-plasmid DNA is transfected into human 293 cells together with helper adenovirus particles. We have taken advantage of this experimental system to analyze the effects of several classes of mutations on replication of AAV DNA. We obtained AAV mutants by molecular cloning in bacterial plasmids of naturally occurring AAV variant or defective-interfering genomes. Each of these mutants contains a single internal deletion of AAV coding sequences. Also, some of these mutant-AAV plasmids have additional deletions of one or both AAV terminal palindromes introduced during constructions in vitro. We show here that AAV mutants containing internal deletions were defective for replicative form DNA replication (rep-) but could be complemented by intact wild-type AAV. This indicates that an AAV replication function, Rep, is required for normal AAV replication. Mutants in which both terminal palindromes were deleted (ori-) were also replication defective but were not complementable by wild-type AAV. The cis-dominance of the ori- mutation shows that the replication origin is comprised in part of the terminal palindrome. Deletion of only one terminal palindrome was phenotypically wild-type and allowed rescue and replication of AAV genomes in which the deleted region was regenerated apparently by an intramolecular correction mechanism. One model for this correction mechanism is proposed. An AAV ori- mutant also complemented replication of AAV rep- mutants as efficiently as did wild-type AAV. These studies also revealed an unexpected additional property of the deletion mutants in that monomeric single-stranded single-stranded DNA accumulated very inefficiently even though monomeric single-stranded DNA from the complementing wild-type AAV did accumulate.
当整个腺相关病毒(AAV)基因组插入细菌质粒中时,将重组AAV - 质粒DNA与辅助腺病毒颗粒一起转染到人293细胞中,即可拯救并复制有感染性的AAV基因组。我们利用这个实验系统来分析几类突变对AAV DNA复制的影响。我们通过在细菌质粒中对天然存在的AAV变体或缺陷干扰基因组进行分子克隆获得了AAV突变体。这些突变体中的每一个都包含AAV编码序列的单个内部缺失。此外,其中一些突变型AAV质粒在体外构建过程中还引入了一个或两个AAV末端回文序列的额外缺失。我们在此表明,含有内部缺失的AAV突变体在复制型DNA复制方面存在缺陷(rep-),但可被完整的野生型AAV互补。这表明正常的AAV复制需要一种AAV复制功能,即Rep。两个末端回文序列都缺失的突变体(ori-)在复制方面也存在缺陷,但不能被野生型AAV互补。ori-突变的顺式显性表明复制起点部分包含在末端回文序列中。仅缺失一个末端回文序列在表型上是野生型的,并且允许AAV基因组的拯救和复制,其中缺失区域显然通过分子内校正机制得以再生。为此校正机制提出了一个模型。一个AAV ori-突变体对AAV rep-突变体复制的互补效率与野生型AAV一样高。这些研究还揭示了缺失突变体一个意外的额外特性,即单体单链DNA积累效率非常低,尽管来自互补野生型AAV的单体单链DNA确实会积累。