Generation of m.3177 G > A mutant mice.

<p><b>(A)</b> The experimental workflow for generating the m.3177 G > A mice by injecting base editing tool-DdCBE-3177 mRNAs- into zygotes and selection of high heteroplasmy lines without off-targeting. <b>(B)</b> Homology of the human Leber hereditary optic neuropat...

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Main Author: Qin Xie (93388) (author)
Other Authors: Haibo Wu (156272) (author), Jiaxin Qiu (12693251) (author), Junbo Liu (408294) (author), Xueyi Jiang (11257734) (author), Huihui Wu (531100) (author), Qifeng Lyu (736115) (author), Hui Long (525973) (author), Wenzhi Li (617452) (author), Shuo Zhang (30844) (author), Yuxiao Zhou (4173652) (author), Yining Gao (12496273) (author), Aaron J. W. Hsueh (22772686) (author), Yanping Kuang (736116) (author), Lun Suo (838212) (author)
Published: 2025
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Summary:<p><b>(A)</b> The experimental workflow for generating the m.3177 G > A mice by injecting base editing tool-DdCBE-3177 mRNAs- into zygotes and selection of high heteroplasmy lines without off-targeting. <b>(B)</b> Homology of the human Leber hereditary optic neuropathy mtDNA mutation m.3733 G > A and corresponding mouse mutant selected. <b>(C)</b> Lack of off-targeting in the mtDNA genome in the F1 m.3177 G > A mice with the heteroplasmy of 6.72%. A wildtype (WT) mouse was used as the control. <b>(D)</b> The heteroplasmy among different tissues in m.3177 G > A mice. F represent generation and m represent mice age in months.</p>