Senapathy P, Carter B J
J Biol Chem. 1984 Apr 10;259(7):4661-6.
Continued passage of the human parvovirus, adeno-associated virus (AAV), at high multiplicity of infection in human cells results in the accumulation of AAV particles containing variant genomes. We have analyzed the structure of individual variant AAV genomes by molecular cloning in the Escherichia coli plasmid, pBR328. Each of the AAV inserts in six individual recombinant plasmids contained a single internal deletion but in contrast to a previous model, the locations of the deletions were nonrandom. The molecular cloning protocol also generated recombinant plasmids containing the entire AAV2 DNA sequence which yielded infectious AAV particles when transfected into human 293 cells in the presence of helper adenovirus using a DEAE-transfection procedure. Infectious AAV genomes were also generated by recombination when cells were jointly transfected with a mixture of plasmids containing two different mutant AAV genomes. The efficiency of this recombination appear to be influenced by the degree of homology between the mutant AAV genomes.
人类细小病毒腺相关病毒(AAV)在人细胞中以高感染复数持续传代,会导致含有变异基因组的AAV颗粒积累。我们通过在大肠杆菌质粒pBR328中进行分子克隆,分析了单个变异AAV基因组的结构。六个独立重组质粒中的每个AAV插入片段都包含一个单一的内部缺失,但与之前的模型不同,缺失的位置并非随机。分子克隆方案还产生了包含完整AAV2 DNA序列的重组质粒,当使用DEAE转染程序在辅助腺病毒存在的情况下将其转染到人293细胞中时,可产生有感染性的AAV颗粒。当用含有两种不同突变AAV基因组的质粒混合物共同转染细胞时,通过重组也可产生有感染性的AAV基因组。这种重组的效率似乎受突变AAV基因组之间同源程度的影响。