Massie B, Couture F, Lamoureux L, Mosser D D, Guilbault C, Jolicoeur P, Bélanger F, Langelier Y
Institut de Recherches en Biotechnologie, Montréal, Québec, Canada.
J Virol. 1998 Mar;72(3):2289-96. doi: 10.1128/JVI.72.3.2289-2296.1998.
We have constructed two new adenovirus expression cassettes that expand both the range of genes which can be expressed with adenovirus vectors (AdV) and the range of cells in which high-level expression can be attained. By inclusion of a tetracycline-regulated promoter in the transfer vector pAdTR5, it is now possible to generate recombinant adenoviruses expressing proteins that are either cytotoxic or that interfere with adenovirus replication. We have used this strategy to generate a recombinant adenovirus encoding a deletion in the R1 subunit [R1(delta2-357)] of the herpes simplex virus type 2 ribonucleotide reductase. Cell lines expressing the tetracycline-regulated transactivator (tTA) from an integrated vector or following infection with an AdV expressing tTA are able to produce deltaR1 protein at a level approaching 10% total cell protein (TCP) when infected with Ad5TR5 deltaR1 before they subsequently die. To our knowledge, this is the first report of the overexpression of a toxic gene product with AdV. We have also constructed a new constitutive adenovirus expression cassette based on an optimized cytomegalovirus immediate-early promoter-enhancer that allows the expression of recombinant proteins at a level greater than 20% TCP in nonpermissive cell lines. Together, these new expression cassettes significantly improve the utility of the adenovirus system for high-level expression of recombinant proteins in animal cells and will undoubtedly find useful applications in gene therapy.
我们构建了两个新的腺病毒表达盒,它们扩大了可用腺病毒载体(AdV)表达的基因范围以及能够实现高水平表达的细胞范围。通过在转移载体pAdTR5中加入四环素调控启动子,现在有可能产生表达具有细胞毒性或干扰腺病毒复制的蛋白质的重组腺病毒。我们已采用这一策略来产生一种重组腺病毒,其编码单纯疱疹病毒2型核糖核苷酸还原酶R1亚基中的缺失片段[R1(δ2 - 357)]。从整合载体表达四环素调控反式激活因子(tTA)或在用表达tTA的AdV感染后表达tTA的细胞系,在被Ad5TR5 δR1感染随后死亡之前,能够产生接近总细胞蛋白(TCP)10%水平的δR1蛋白。据我们所知,这是关于用AdV过表达毒性基因产物的首次报道。我们还基于优化的巨细胞病毒立即早期启动子 - 增强子构建了一个新的组成型腺病毒表达盒,其能在非允许细胞系中以大于20% TCP的水平表达重组蛋白。总之,这些新的表达盒显著提高了腺病毒系统在动物细胞中高水平表达重组蛋白的效用,并且无疑将在基因治疗中找到有用的应用。