Collarini Ellen J, Leighton Philip A, Van de Lavoir Marie-Cecile
Ligand Pharmaceuticals, Inc., Emeryville, CA, USA.
Methods Mol Biol. 2019;1874:403-430. doi: 10.1007/978-1-4939-8831-0_24.
The unique characteristics of the avian embryo, with its large opaque yolk, have necessitated the development of different approaches to transgenesis from those that have been successful in mammalian species. Genetic modification of birds was greatly advanced by the ability to grow long-term cultures of primordial germ cells (PGCs). These cells are obtained from embryos, established in culture, and can be propagated without losing the ability to contribute to the germline when reintroduced into a host animal. PGCs can be genetically modified in culture using traditional transfection and selection techniques, including gene targeting and site-specific nuclease approaches. Here, we describe our methods for deriving cell lines, long-term culture, genetic modification, production of germline chimeras and obtaining fully transgenic birds with the desired genetic modifications.
鸟类胚胎具有独特的特征,其卵黄大且不透明,这就需要开发不同于在哺乳动物中成功应用的转基因方法。能够长期培养原始生殖细胞(PGC)极大地推动了鸟类的基因改造。这些细胞从胚胎中获取,在培养中建立起来,并且在重新引入宿主动物后能够增殖而不丧失对生殖系的贡献能力。PGC可以在培养中使用传统的转染和筛选技术进行基因改造,包括基因靶向和位点特异性核酸酶方法。在这里,我们描述了我们用于获得细胞系、长期培养、基因改造、生产生殖系嵌合体以及获得具有所需基因改造的完全转基因鸟类的方法。