Ding Sheng, Xu Tian, Wu Xiaohui
State Key Laboratory of Genetic Engineering and Institute of Developmental Biology and Molecular Medicine, Fudan-Yale Biomedical Research Center, School of Life Sciences, Fudan University, Shanghai, 200433, China.
Methods Mol Biol. 2014;1194:171-85. doi: 10.1007/978-1-4939-1215-5_9.
Genetically engineered mice (GEM) are invaluable tools not only for understanding mammalian biology but also for modeling human diseases. Here we present protocols to generate GEM with the piggyBac (PB) transposon system. In the first part, we describe a transgenic procedure that co-injects the transgene carried by a PB donor plasmid and a PB transposase (PBase)-expressing helper plasmid into the pronuclei of fertilized eggs. In the second part, we provide a large-scale, cost-effective insertional mutagenesis strategy that remobilizes single-copy PB transposons in the male germ line. Given that PB can transpose in a broad spectrum of eukaryotic hosts, the protocols described here could be adapted for other species in the future.
基因工程小鼠(GEM)不仅是理解哺乳动物生物学的宝贵工具,也是人类疾病建模的重要手段。在此,我们介绍利用piggyBac(PB)转座子系统生成基因工程小鼠的方法。第一部分,我们描述了一种转基因程序,即将PB供体质粒携带的转基因与表达PB转座酶(PBase)的辅助质粒共同注射到受精卵的原核中。第二部分,我们提供了一种大规模、经济高效的插入诱变策略,该策略可在雄性生殖系中重新激活单拷贝PB转座子。鉴于PB可在广泛的真核宿主中进行转座,这里描述的方法未来可能适用于其他物种。