Nakaya Masataka, Iwatani Chizuru, Tsukiyama-Fujii Setsuko, Mieda Ai, Tarumoto Shoko, Tsujimura Taro, Yamamoto Takuya, Ichikawa Takafumi, Nakamura Tomonori, Terakado Ichiro, Kawamoto Ikuo, Nakagawa Takahiro, Itagaki Iori, Saitou Mitinori, Tsuchiya Hideaki, Tsukiyama Tomoyuki
Research Center for Animal Life Science, Shiga University of Medical Science, Shiga, Japan.
Institute for the Advanced Study of Human Biology (WPI-ASHBi), Kyoto University, Kyoto, Japan.
Nat Commun. 2025 Mar 24;16(1):2179. doi: 10.1038/s41467-025-57365-w.
Non-human primates, such as cynomolgus monkeys, are invaluable experimental models for understanding human biology and disease. Their close genetic relationship to humans makes them essential for studying fundamental human developmental processes and disease progression. Although lentiviral methods for generating transgenic monkeys exist, several inherent technical difficulties limit their utility. To solve this problem, here we establish a non-viral method for generating transgenic cynomolgus monkeys using the piggyBac transposon system. After optimizing our protocol in mice, we show that the co-injection of piggyBac components with sperm into metaphase II-stage oocytes successfully generates transgenic monkeys expressing transgenes throughout their whole bodies. Transgene expression is observed in all examined tissue types, including germ cells, although the levels of expression vary. Insertion analysis further confirms the successful integration of the transgene. We propose that our method will be a practical non-viral protocol for generating transgenic non-human primates.
食蟹猴等非人灵长类动物是理解人类生物学和疾病的宝贵实验模型。它们与人类密切的遗传关系使其对于研究人类基本发育过程和疾病进展至关重要。尽管存在用于生成转基因猴的慢病毒方法,但一些固有的技术难题限制了它们的实用性。为了解决这个问题,我们在此建立了一种使用piggyBac转座子系统生成转基因食蟹猴的非病毒方法。在小鼠中优化我们的方案后,我们表明将piggyBac组件与精子共注射到中期II期卵母细胞中能够成功生成全身表达转基因的转基因猴。在所有检测的组织类型中都观察到了转基因表达,包括生殖细胞,尽管表达水平有所不同。插入分析进一步证实了转基因的成功整合。我们认为我们的方法将是一种用于生成转基因非人灵长类动物的实用非病毒方案。