Vilaboa Nuria, Fenna Mary, Munson John, Roberts Stephen M, Voellmy Richard
Laboratorio de Metabolismo Oseo, Hospital Universitario La Paz, Paseo de la Castellana 261, 28046 Madrid, Spain.
Mol Ther. 2005 Aug;12(2):290-8. doi: 10.1016/j.ymthe.2005.03.029.
This article reports on the construction and analysis in vitro and in vivo of novel gene switches that can be used to achieve spatial as well as temporal control over the expression of a transgene of interest. The switches are expected to be functional in virtually any tissue and cell type. They consist of (a) a foreign or modified transactivator expressed under the dual control of a promoter or promoter cassette that is responsive to heat and the transactivator and (b) a promoter responsive to the transactivator for controlling the transgene of interest. A preferred gene switch of this type incorporated a mifepristone-dependent transactivator. This gene switch could be activated by a transient heat treatment in the presence of mifepristone. Activity increased with the intensity of the activating heat treatment and was found to persist for more than 6 days. The gene switch was essentially inactive prior to an activating heat treatment, in the absence or presence of mifepristone. Activated gene switch could be silenced by removal/withdrawal of mifepristone.
本文报道了新型基因开关的体外构建及体内外分析,这些基因开关可用于实现对目的转基因表达的空间和时间控制。预计这些开关在几乎任何组织和细胞类型中都能发挥作用。它们由(a)在对热和反式激活因子有反应的启动子或启动子盒的双重控制下表达的外源或修饰的反式激活因子,以及(b)对反式激活因子有反应的用于控制目的转基因的启动子组成。这种类型的一种优选基因开关包含一种米非司酮依赖性反式激活因子。这种基因开关可在米非司酮存在的情况下通过短暂热处理激活。活性随激活热处理的强度增加而增加,并且发现可持续超过6天。在进行激活热处理之前,无论是否存在米非司酮,该基因开关基本无活性。通过去除/停用米非司酮可使激活的基因开关沉默。