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Germline transgenesis in rabbits by pronuclear microinjection of Sleeping Beauty transposons

机译:睡眠美容转座子的原核显微注射在家兔中进行生殖系转基因

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摘要

The laboratory rabbit (Oryctolagus cuniculus) is widely used as a model for a variety of inherited and acquired human diseases.\udIn addition, the rabbit is the smallest livestock animal that is used to transgenically produce pharmaceutical proteins in its milk. Here we describe a protocol for high-efficiency germline transgenesis and sustained transgene expression in rabbits by using\udthe Sleeping Beauty (SB) transposon system. The protocol is based on co-injection into the pronuclei of fertilized oocytes of synthetic mRNARNARNA encoding the SB100X hyperactive transposase together with plasmid DNANA carrying a transgene construct flanked by binding sites for the transposase. The translation of the transposase mRNARNARNA is followed by enzyme-mediated excision of the transgene cassette from the plasmids and its permanent genomic insertion to produce stable transgenic animals. Generation of a germline-transgenic founder animal by using this protocol takes ~2 months. Transposon-mediated transgenesis compares favorably in terms of both efficiency and reliable transgene expression with classic pronuclear microinjection, and it offers comparable efficacies (numbers of transgenic founders obtained per injected embryo) to lentiviral approaches, without limitations on vector design, issues of transgene silencing, and the toxicity and biosafety concerns of working with viral vectors.
机译:实验室兔(穴兔(Oryctolagus cuniculus))被广泛用作各种遗传性和后天性人类疾病的模型。\ ud此外,兔子是最小的牲畜,用于在乳汁中转基因生产药物蛋白。在这里,我们描述了通过使用“睡美人”(SB)转座子系统在兔中进行高效种系转基因和持续转基因表达的方案。该方案基于将编码SB100X高活性转座酶的合成mRNARNARNA与携带侧翼为转座酶结合位点的转基因构建体的质粒DNANA共注入受精卵母细胞的前核中。转座酶mRNARNARNA的翻译后,是从质粒中经酶介导切除转基因盒及其永久性基因组插入,以产生稳定的转基因动物。使用此协议生成种系转基因创始人动物大约需要2个月的时间。转座子介导的转基因在效率和可靠的转基因表达方面均优于经典的原核显微注射,并且可提供与慢病毒方法相当的功效(每个注射的胚胎获得的转基因创始人数量),而不受载体设计,转基因沉默,以及使用病毒载体的毒性和生物安全性问题。

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