Ochiai H, Fujimuro M, Yokosawa H, Harashima H, Kamiya H
Faculty of Pharmaceutical Sciences, Hokkaido University, Kita-ku, Sapporo, Japan.
Gene Ther. 2007 Aug;14(15):1152-9. doi: 10.1038/sj.gt.3302970. Epub 2007 May 24.
The intranuclear disposition of exogenous DNA is quite important for the therapeutic effects of the administered DNA. The expression efficiency from one copy of exogenous DNA delivered by hydrodynamics-based injection dramatically decreases over time, and this 'silencing' occurs without CpG methylation. In this study, naked luciferase-plasmid DNA was delivered into mouse liver by hydrodynamics-based injection, and modifications of the histones bound to the plasmid DNA were analyzed by a chromatin immunoprecipitation (ChIP) analysis. In addition, the effects of a second hydrodynamics-based injection on the expression from the plasmid DNA were examined. The ChIP analysis revealed that the modification status of histone H3 remained constant from 4 h to 4 weeks. Surprisingly, the injection of saline without DNA enhanced the luciferase expression from the preexisting DNA administered 4 and 14 days previously. Our results suggest that histone modification plays no role in the silencing. Instead, our data suggest that the transgene expression is activated by the hydrodynamics-based injection manipulation, and that the return from the activated status causes the silencing.
外源性DNA的核内定位对于所给予DNA的治疗效果非常重要。通过基于流体动力学的注射递送的一份外源性DNA的表达效率会随着时间显著降低,并且这种“沉默”在没有CpG甲基化的情况下发生。在本研究中,通过基于流体动力学的注射将裸荧光素酶 - 质粒DNA递送至小鼠肝脏,并通过染色质免疫沉淀(ChIP)分析来分析与质粒DNA结合的组蛋白的修饰。此外,还研究了第二次基于流体动力学的注射对质粒DNA表达的影响。ChIP分析显示组蛋白H3的修饰状态在4小时至4周内保持不变。令人惊讶的是,注射不含DNA的盐水增强了4天和14天前给予的预先存在的DNA的荧光素酶表达。我们的结果表明组蛋白修饰在沉默中不起作用。相反,我们的数据表明转基因表达是由基于流体动力学的注射操作激活的,并且从激活状态的恢复导致沉默。