摘要
目的:构建一种肝脏高效表达调控元件,促进水动力转染外源基因在体内的长期高效表达。方法:构建了以hAAT基因作为报告基因,分别含有表达调控元件AerApoEAATP、ApoEAATP、A lbEAATP及CMV启动子的真核表达载体pC Ineo-AerApoEAATP-hAAT、pC Ineo-ApoEAATP-hAAT、pC Ineo-A lbEAATP-hAAT及pC Ineo-hAAT,水动力转染法将上述质粒分别转染BALB/c小鼠,定期检测小鼠血清中hAAT的浓度反应AerApoEAATP、ApoEAATP、A l-bEAATP及CMV的调控能力。结果与结论:所构建的表达调控元件AerApoEAATP具有较强的调控能力,其长期的调控水平高于CMV、A lbEAATP和ApoEAATP。
Objective: To construct a liver highly-effective control element that can prolong the expression time of hydrodynamically transfected gene. Methods: Plasmid pCIneo-AerApoEAATP-hAAT, pCIneo-ApoEAATP-hAAT, pCIneo-Al- bEAATP-hAAT and pCIneo hAAT were constructed respectively. All of them included hAAT gene as the reporter gene. BALB/c mice were transfected with the plasmids by hydrodynamical transfection technology. The activity of AerApoEAATP, ApoEAATP,AlbEAATP and CMV was compared by the concentration of hAAT. Results and Conclusion: The control element constructed is much stronger than ApoEAATP,AlbEAATP and CMV in the long-term expression.
出处
《军事医学科学院院刊》
CSCD
北大核心
2006年第3期206-208,229,共4页
Bulletin of the Academy of Military Medical Sciences
基金
国家自然科学基金
北京市自然科学基金资助项目(30300184
30400561
7063086)