Liu Chengyu, Xie Wen, Gui Changyun, Du Yubin
iPSC and Genome Engineering Core, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD, USA.
Methods Mol Biol. 2013;1027:217-32. doi: 10.1007/978-1-60327-369-5_10.
Transgenic mouse technology is a powerful method for studying gene function and creating animal models of human diseases. Currently, the most widely used method for generating transgenic mice is the pronuclear microinjection method. In this method, a transgenic DNA construct is physically microinjected into the pronucleus of a fertilized egg. The injected embryos are subsequently transferred into the oviducts of pseudopregnant surrogate mothers. A portion of the mice born to these surrogate mothers will harbor the injected foreign gene in their genomes. These procedures are technically challenging for most biomedical researchers. Inappropriate experimental procedures or suboptimal equipment setup can substantially reduce the efficiency of transgenic mouse production. In this chapter, we describe in detail our microinjection setup as well as our standard microinjection and oviduct transfer procedures.
转基因小鼠技术是研究基因功能和创建人类疾病动物模型的一种强大方法。目前,生成转基因小鼠最广泛使用的方法是原核显微注射法。在这种方法中,将转基因DNA构建体物理显微注射到受精卵的原核中。随后将注射后的胚胎转移到假孕代孕母鼠的输卵管中。这些代孕母鼠所生的一部分小鼠将在其基因组中携带注射的外源基因。对于大多数生物医学研究人员来说,这些操作在技术上具有挑战性。不适当的实验程序或欠佳的设备设置会大幅降低转基因小鼠的生产效率。在本章中,我们将详细描述我们的显微注射设置以及标准的显微注射和输卵管转移程序。