Department of Molecular Life Science, Division of Basic Medical Science and Molecular Medicine, Tokai University School of Medicine, 143 Shimokasuya, Isehara, Kanagawa 259-1193, Japan.
Nucleic Acids Res. 2010 Dec;38(22):e198. doi: 10.1093/nar/gkq860. Epub 2010 Sep 29.
Mouse transgenesis has proven invaluable for analysis of gene function and generation of human disease models. We describe here the development of a pronuclear injection-based targeted transgenesis (PITT) system, involving site-specific integration in fertilized eggs. The system was applied to two different genomic target loci to generate a series of transgenic lines including fluorescent mice, which reproducibly displayed strong, ubiquitous and stable transgene expression. We also demonstrated that knockdown mice could be readily generated by PITT by taking advantage of the reproducible and highly efficient expression system. The PITT system, which circumvents the problem of unpredictable and unstable transgene expression of conventional random-integration transgenic mice, reduces the time, cost and effort needed to generate transgenic mice, and is potentially applicable to both in vivo 'gain-of-function' and 'loss-of-function' studies.
小鼠转基因技术已被证明在分析基因功能和产生人类疾病模型方面具有不可估量的价值。我们在这里描述了一种基于原核注射的靶向转基因(PITT)系统的开发,该系统涉及在受精卵中进行特异性整合。该系统应用于两个不同的基因组靶标位点,生成了一系列转基因品系,包括荧光小鼠,这些小鼠可重复地显示出强烈、普遍和稳定的转基因表达。我们还证明,通过利用可重复和高效的表达系统,PITT 可以很容易地生成基因敲低小鼠。PITT 系统避免了传统随机整合转基因小鼠中不可预测和不稳定的转基因表达问题,减少了生成转基因小鼠所需的时间、成本和精力,并且可能适用于体内“功能获得”和“功能丧失”研究。