Wang Y, Krushel L A, Edelman G M
Department of Neurobiology, Scripps Research Institute, La Jolla, CA 92037, USA.
Proc Natl Acad Sci U S A. 1996 Apr 30;93(9):3932-6. doi: 10.1073/pnas.93.9.3932.
Conditional gene expression and gene deletion are important experimental approaches for examining the functions of particular gene products in development and disease. The cre-loxP system from bacteriophage P1 has been used in transgenic animals to induce site-specific DNA recombination leading to gene activation or deletion. To regulate the recombination in a spatiotemporally controlled manner, we constructed a recombinant adenoviral vector, Adv/cre, that contained the cre recombinase gene under regulation of the herpes simplex virus thymidine kinase promoter. The efficacy and target specificity of this vector in mediating loxP-dependent recombination were analyzed in mice that had been genetically engineered to contain loxP sites in their genome. After intravenous injection of the Adv/cre vector into adult animals, the liver and spleen showed the highest infectivity of the adenovirus as well as the highest levels of recombination, whereas other tissues such as kidney, lung, and heart had lower levels of infection and recombination. Only trace levels of recombination were detected in the brain. However, when the Adv/cre vector was injected directly into specific regions of the adult brain, including the cerebral cortex, hippocampus, and cerebellum, recombination was detectable at the injection site. Furthermore, when the Adv/cre vector was injected into the forebrains of neonatal mice, the rearranged toxP locus from recombination could be detected in the injected regions for at least 8 weeks. Taken together, these results demonstrate that the Adv/cre vector expressing a functional cre protein is capable of mediating loxP-dependent recombination in various tissues and the recombined gene locus may in some cases be maintained for an extended period. The use of the adenovirus vector expressing cre combined with localized delivery to specific tissues may provide an efficient means to achieve conditional gene expression or knockout with precise spatiotemporal control.
条件性基因表达和基因缺失是研究特定基因产物在发育和疾病中功能的重要实验方法。来自噬菌体P1的cre-loxP系统已被用于转基因动物中,以诱导位点特异性DNA重组,从而导致基因激活或缺失。为了以时空可控的方式调节重组,我们构建了一种重组腺病毒载体Adv/cre,其在单纯疱疹病毒胸苷激酶启动子的调控下包含cre重组酶基因。在基因组中经过基因工程改造含有loxP位点的小鼠中,分析了该载体介导loxP依赖性重组的效率和靶标特异性。将Adv/cre载体静脉注射到成年动物体内后,肝脏和脾脏显示出最高的腺病毒感染性以及最高水平的重组,而肾脏、肺和心脏等其他组织的感染和重组水平较低。在大脑中仅检测到痕量水平的重组。然而,当将Adv/cre载体直接注射到成年大脑的特定区域,包括大脑皮层、海马体和小脑时,在注射部位可检测到重组。此外,当将Adv/cre载体注射到新生小鼠的前脑中时,在注射区域至少8周内都能检测到来自重组的重排loxP位点。综上所述,这些结果表明表达功能性cre蛋白的Adv/cre载体能够在各种组织中介导loxP依赖性重组,并且在某些情况下重组的基因位点可能会维持较长时间。使用表达cre的腺病毒载体并结合向特定组织的局部递送,可能提供一种在精确的时空控制下实现条件性基因表达或基因敲除的有效方法。