基因敲除
清脆的
生物
基因敲除
计算生物学
基因
基因靶向
轴突
基因组编辑
Cas9
功能(生物学)
基因剔除小鼠
遗传学
再生(生物学)
等位基因
作者
Liqun Wang,Yan-Yun Zeng,Yanmei Liu,Ji‐Feng Fei
标识
DOI:10.1007/978-1-0716-2659-7_23
摘要
Tetrapod species axolotls exhibit the powerful capacity to fully regenerate their tail and limbs upon injury, hence serving as an excellent model organism in regenerative biology research. Developing proper molecular and genetic tools in axolotls is an absolute necessity for deep dissection of tissue regeneration mechanisms. Previously, CRISPR-/Cas9-based knockout and targeted gene knock-in approaches have been established in axolotls, allowing genetically deciphering gene function, labeling, and tracing particular types of cells. Here, we further extend the CRISPR/Cas9 technology application and describe a method to create reporter-tagged knockout allele in axolotls. This method combines gene knockout and knock-in and achieves loss of function of a given gene and simultaneous labeling of cells expressing this particular gene, that allows identification, tracking of the "knocking out" cells. Our method offers a useful gene function analysis tool to the field of axolotl developmental and regenerative research.
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