Vassaux G, Hurst H C, Lemoine N R
ICRF Molecular Oncology Unit, Imperial College School of Medicine, Hammersmith Campus, Du Cane Road, London W12 0NN, UK.
Gene Ther. 1999 Jun;6(6):1192-7. doi: 10.1038/sj.gt.3300910.
Replication-defective recombinant adenoviruses provide an efficient system for in vivo gene transfer and numerous studies have demonstrated that this vector can accommodate tissue-specific promoters to restrict the expression of a transgene to a particular subset of cells. However, in some cases the selectivity of expression is lost when the tissue-specific promoter is placed in an adenoviral environment. In an attempt to restore the conditionality of expression of the transgene driven by the human ERBB2 promoter, we have flanked the expression cassette in 5' and 3' orientations with a 250 bp sequence containing the bovine growth hormone transcriptional stop signal for cloning into a recombinant adenovirus. The data presented here clearly demonstrate that these 'insulator' elements are able to restrict the expression of the transgene (herpes simplex thymidine kinase) to ERBB2-expressing cells and therefore to restore the selectivity mediated by the ERBB2 promoter. This approach could be generally useful to insulate expression cassettes in adenoviral vectors.
复制缺陷型重组腺病毒为体内基因转移提供了一个高效系统,并且大量研究已证明该载体可容纳组织特异性启动子,从而将转基因的表达限制在特定细胞亚群中。然而,在某些情况下,当将组织特异性启动子置于腺病毒环境中时,表达的选择性会丧失。为了恢复由人ERBB2启动子驱动的转基因表达的条件性,我们在表达盒的5'和3'方向侧翼插入了一段250 bp的序列,该序列包含牛生长激素转录终止信号,用于克隆到重组腺病毒中。此处呈现的数据清楚地表明,这些“绝缘子”元件能够将转基因(单纯疱疹病毒胸苷激酶)的表达限制在表达ERBB2的细胞中,从而恢复由ERBB2启动子介导的选择性。这种方法通常可用于在腺病毒载体中隔离表达盒。