Urabe Masashi, Kogure Katsuhiro, Kume Akihiro, Sato Yuko, Tobita Kiyotake, Ozawa Keiya
Department of Virology, Jichi Medical School, Tochigi 329-0498, Japan.
CREST, Japan Science and Technology Corporation (JST), Tochigi 329-0498, Japan.
J Gen Virol. 2003 Aug;84(Pt 8):2127-2132. doi: 10.1099/vir.0.19193-0.
Adeno-associated virus type 2 integrates preferentially into the AAVS1 locus on chromosome 19 of the human genome. It was reported previously that transfection with two plasmids, one for Rep and the other carrying a transgene flanked by inverted terminal repeats (ITRs), enables preferential integration of the latter into AAVS1. Aiming at increasing the frequency of AAVS1-specific integration, the Rep- to transgene-plasmid ratio necessary to achieve a higher frequency of site-specific integration was examined. 293 cells were co-transfected with the Rep78 plasmid and an ITR-flanked Neo gene at different ratios. G418-resistant clones were selected randomly. Extensive Southern blot analysis showed an optimum range of Rep78 expression. In that range, approximately 20 % of clones harboured the Neo gene at AAVS1. Excess Rep expression, however, resulted in 'abortive' integration of the Neo gene, a rearrangement of AAVS1 without transgene integration. Rep78 appeared to cause abortive integration more extensively than Rep68. Deleterious effects of the Rep protein on the AAVS1 locus should be considered to develop an improved AAVS1-targeted system.
2型腺相关病毒优先整合到人类基因组19号染色体上的AAVS1位点。此前有报道称,用两种质粒转染,一种用于Rep,另一种携带由反向末端重复序列(ITR)侧翼的转基因,可使后者优先整合到AAVS1中。为了提高AAVS1特异性整合的频率,研究了实现更高频率位点特异性整合所需的Rep与转基因质粒的比例。将Rep78质粒和ITR侧翼的Neo基因以不同比例共转染293细胞。随机选择G418抗性克隆。广泛的Southern印迹分析显示了Rep78表达的最佳范围。在该范围内,约20%的克隆在AAVS1处携带Neo基因。然而,过量的Rep表达导致Neo基因的“流产”整合,即AAVS1的重排而无转基因整合。Rep78似乎比Rep68更广泛地导致流产整合。在开发改进的AAVS1靶向系统时,应考虑Rep蛋白对AAVS1位点的有害影响。