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应用敲入策略在蝾螈中创建带有报告基因标签的敲除等位基因。

Applying a Knock-In Strategy to Create Reporter-Tagged Knockout Alleles in Axolotls.

机构信息

Key Laboratory of Brain, Cognition and Education Sciences, Ministry of Education; Institute for Brain Research and Rehabilitation, South China Normal University, Guangzhou, China.

Department of Pathology, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China.

出版信息

Methods Mol Biol. 2023;2562:351-368. doi: 10.1007/978-1-0716-2659-7_23.

Abstract

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.

摘要

蝾螈物种的墨西哥钝口螈具有在受伤后完全再生其尾巴和肢体的强大能力,因此是再生生物学研究中的优秀模式生物。在墨西哥钝口螈中开发适当的分子和遗传工具对于深入剖析组织再生机制是绝对必要的。以前,已经在墨西哥钝口螈中建立了基于 CRISPR/Cas9 的敲除和靶向基因敲入方法,从而能够对基因功能、标记和追踪特定类型的细胞进行基因解码。在这里,我们进一步扩展了 CRISPR/Cas9 技术的应用,并描述了一种在墨西哥钝口螈中创建报告基因标记敲除等位基因的方法。该方法结合了基因敲除和敲入,实现了特定基因的功能丧失和同时标记表达该特定基因的细胞,从而可以识别和追踪“敲除”细胞。我们的方法为墨西哥钝口螈发育和再生研究领域提供了一种有用的基因功能分析工具。

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