Laboratory of Molecular Genetics, Institute of Medical Science, University of Tokyo, Tokyo, Japan.
Nucleic Acids Res. 2011 Jan;39(2):e7. doi: 10.1093/nar/gkq966. Epub 2010 Nov 4.
Tissue-/cancer-specific promoters for use in adenovirus vectors (AdVs) are valuable for elucidating specific gene functions and for use in gene therapy. However, low activity, non-specific expression and size limitations in the vector are always problems. Here, we developed a 'double-unit' AdV containing the Cre gene under the control of an α-fetoprotein promoter near the right end of its genome and bearing a compact 'excisional-expression' unit consisting of a target cDNA 'upstream' of a potent promoter between two loxPs near the left end of its genome. When Cre was expressed, the expression unit was excised as a circular molecule and strongly expressed. Undesired leak expression of Cre during virus preparation was completely suppressed by a dominant-negative Cre and a short-hairpin RNA against Cre. Using this novel construct, a very strict specificity was maintained while achieving a 40- to 90-fold higher expression level, compared with that attainable using a direct specific promoter. Therefore, the 'double-unit' AdV enabled us to produce a tissue-/cancer-specific promoter in an AdV with a high expression level and strict specificity.
组织/肿瘤特异性启动子可用于腺病毒载体(AdVs),对于阐明特定基因功能和基因治疗非常有用。然而,载体中的低活性、非特异性表达和大小限制始终是问题。在这里,我们开发了一种“双单位”AdV,其基因组右侧末端附近的 Cre 基因受甲胎蛋白启动子的控制,并且带有一个紧凑的“切除表达”单元,该单元由基因组左侧末端附近的两个loxP 之间的有效启动子上游的靶 cDNA 组成。当表达 Cre 时,表达单元被切除为一个环状分子,并强烈表达。在病毒制备过程中,通过显性负性 Cre 和针对 Cre 的短发夹 RNA 完全抑制 Cre 的非必需泄漏表达。使用这种新型构建体,与使用直接特异性启动子时相比,可维持非常严格的特异性,同时实现 40 到 90 倍的更高表达水平。因此,“双单位”AdV 使我们能够在具有高表达水平和严格特异性的 AdV 中产生组织/肿瘤特异性启动子。