Zheng Changyu, Baum Bruce J
Gene Therapy and Therapeutics Branch, NIDCR, NIH, DHHS, Bethesda, MD, USA.
Methods Mol Biol. 2008;434:205-19. doi: 10.1007/978-1-60327-248-3_13.
Vectors used in gene therapy require an expression cassette. The expression cassette consists of three important components: promoter, therapeutic gene and polyadenylation signal. The promoter is essential to control expression of the therapeutic gene. A tissue-specific promoter is a promoter that has activity in only certain cell types. Use of a tissue-specific promoter in the expression cassette can restrict unwanted transgene expression as well as facilitate persistent transgene expression. Therefore, choosing the correct promoter, especially a tissue-specific promoter, is a major step toward achieving successful therapeutic transgene expression. Ideally, the elements of the natural promoter region, necessary for obtaining the required level of the gene expression while retaining tissue-specificity, should be known. Also, it is important to understand whether interactions occur between the promoter region and the rest of the vector genome that could affect promoter activity and specificity. To assess this, it is helpful to select a suitable vector system that will be used in further gene therapy studies. Second, have one or several candidate tissue-specific promoters available for use. Third, ideally have an in vitro cell model suitable to evaluate tissue-specificity. Fourth, have a convenient in vivo animal model to use. Fifth, select a good reporter gene system. Next, using conventional recombinant DNA techniques create different promoter constructs with the selected vector system. Lastly, have a suitable transfection method to test the plasmid constructs in both the in vitro and the in vivo models.
基因治疗中使用的载体需要一个表达盒。该表达盒由三个重要组件组成:启动子、治疗性基因和聚腺苷酸化信号。启动子对于控制治疗性基因的表达至关重要。组织特异性启动子是仅在某些细胞类型中具有活性的启动子。在表达盒中使用组织特异性启动子可以限制不必要的转基因表达,并促进转基因的持续表达。因此,选择正确的启动子,尤其是组织特异性启动子,是实现治疗性转基因成功表达的重要一步。理想情况下,应该了解天然启动子区域中获得所需基因表达水平同时保留组织特异性所必需的元件。此外,了解启动子区域与载体基因组的其余部分之间是否发生相互作用从而影响启动子活性和特异性也很重要。为了评估这一点,选择一个将用于进一步基因治疗研究的合适载体系统会有所帮助。其次,要有一个或几个可供使用的候选组织特异性启动子。第三,理想情况下要有一个适合评估组织特异性的体外细胞模型。第四,要有一个方便的体内动物模型可供使用。第五,选择一个良好的报告基因系统。接下来,使用常规重组DNA技术,用选定的载体系统创建不同的启动子构建体。最后,要有一种合适的转染方法,在体外和体内模型中测试质粒构建体。