Fedorov L M, Tyrsin O Y, Sakk O, Ganscher A, Rapp U R
Genesis. 2001 Oct;31(2):78-84. doi: 10.1002/gene.10007.
Despite the overall successful application of the tet-system to regulate gene expression in vitro and in vivo, nothing is known so far about the long-term stability of this system in transgenic mice. In this study, mice of generation F2, F3, F4, or F10 of two independent tTA(CMV) transgenic lines were bred with NZL-2 mice containing a tTA-responsive bidirectional promoter that allows the simultaneous expression of two reporter genes encoding luciferase and beta-galactosidase. Analysis of the expression of transgenes in double transgenic mice revealed a dramatic reduction of tTA transactivator mRNA over time. As a consequence, the expression of both reporter genes was gradually reduced from generation to generation in tissues of embryonic and adult NZL-2/tTA(CMV) mice. Luciferase activity in NZL-2/tTA(CMV)(F10) mice was reduced 8-10-fold compared to NZL-2/ tTA(CMV)(F2) mice, and beta-galactosidase expression was no longer detectable. In summary, we describe the long-term instability of the tet-system in our NZL-2/tTA(CMV) double transgenic mice. The molecular basis of this observation and experimental tools to overcome this limitation need to be addressed in future.
尽管四环素系统在体外和体内调节基因表达方面总体应用成功,但迄今为止,对于该系统在转基因小鼠中的长期稳定性仍一无所知。在本研究中,将两个独立的tTA(CMV)转基因系的F2、F3、F4或F10代小鼠与含有tTA应答双向启动子的NZL-2小鼠进行杂交,该启动子可同时表达编码荧光素酶和β-半乳糖苷酶的两个报告基因。对双转基因小鼠中转基因表达的分析显示,随着时间的推移,tTA反式激活因子mRNA显著减少。因此,在胚胎和成体NZL-2/tTA(CMV)小鼠的组织中,两个报告基因的表达逐代逐渐降低。与NZL-2/tTA(CMV)(F2)小鼠相比,NZL-2/tTA(CMV)(F10)小鼠中的荧光素酶活性降低了8至10倍,且不再能检测到β-半乳糖苷酶的表达。总之,我们描述了在我们的NZL-2/tTA(CMV)双转基因小鼠中四环素系统的长期不稳定性。这一观察结果的分子基础以及克服这一限制的实验工具需要在未来加以探讨。