光遗传学
转基因
转基因小鼠
拉伤
Cre重组酶
重组酶
细胞生物学
基因组
嵌合体(遗传学)
荧光素酶
转基因生物
重组DNA
分子生物学
生物
生物物理学
化学
遗传学
计算生物学
细胞培养
基因
转染
重组
解剖
神经科学
作者
Huiying Li,WU Ying-yin,Yuhao Qiu,Xinru Li,Yuting Guan,Xiya Cao,Meizhen Liu,Dan Zhang,Sijie Huang,Longnian Lin,Lijian Hui,Xueyun Ma,Mingyao Liu,Xueli Zhang,Liren Wang,Dali Li
标识
DOI:10.1002/advs.202201352
摘要
Optogenetic genome engineering is a powerful technology for high-resolution spatiotemporal genetic manipulation, especially for in vivo studies. It is difficult to generate stable transgenic animals carrying a tightly regulated optogenetic system, as its long-term expression induces high background activity. Here, the generation of an enhanced photoactivatable Cre recombinase (ePA-Cre) transgenic mouse strain with stringent light responsiveness and high recombination efficiency is reported. Through serial optimization, ePA-Cre is developed to generate a transgenic mouse line that exhibits 175-fold induction upon illumination. Efficient light-dependent recombination is detected in embryos and various adult tissues of ePA-Cre mice crossed with the Ai14 tdTomato reporter. Importantly, no significant background Cre activity is detected in the tested tissues except the skin. Moreover, efficient light-inducible cell ablation is achieved in ePA-Cre mice crossed with Rosa26-LSL-DTA mice. In conclusion, ePA-Cre mice offer a tightly inducible, highly efficient, and spatiotemporal-specific genome engineering tool for multiple applications.
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