转基因
生物
基因
分子生物学
效价
报告基因
遗传增强
病毒载体
基因传递
紫胶操纵子
腺病毒科
基因表达
病毒学
遗传学
病毒
重组DNA
作者
Masahiro Suzuki,Satoru Kondo,Z Pei,Aya Maekawa,Izumu Saito,Yumi Kanegae
出处
期刊:Gene Therapy
[Springer Nature]
日期:2015-01-15
卷期号:22 (5): 421-429
被引量:39
摘要
The adenovirus vector (AdV) can carry two transgenes in its genome, the therapeutic gene and a reporter gene, for example. The E3 insertion site has often been used for the expression of the second transgene. A transgene can be inserted at six different sites/orientations: E1, E3 and E4 sites, and right and left orientations. However, the best combination of the insertion sites and orientations as for the titers and the expression levels has not sufficiently been studied. We attempted to construct 18 AdVs producing GFP or LacZ gene driven by the EF1α promoter and Cre gene driven by the α-fetoprotein promoter. The AdV containing GFP gene at E3 in the rightward orientation (GFP-E3R) was not available. The LacZ-E3R AdV showed 20-fold lower titer and 50-fold lower level of fiber mRNA than the control E1L AdV. Notably, we found four aberrantly spliced mRNAs in the LacZ-E3L/R AdVs, probably explaining their very low titers. Although the transgene expression levels in the E4R AdVs were about threefold lower than those in the E1L AdVs, their titers are comparable with that of E1L AdVs. We concluded that E1L and E4R sites/orientations are preferable for expressing the main target gene and a second gene, respectively.
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