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利用Cas9 RNA引导核酸酶对小鼠进行工程化碱基改变和表位标签等位基因操作。

Engineering Base Changes and Epitope-Tagged Alleles in Mice Using Cas9 RNA-Guided Nuclease.

作者信息

Gertsenstein Marina, Lintott Lauri G, Nutter Lauryl M J

机构信息

The Centre for Phenogenomics, Toronto, Canada.

Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Canada.

出版信息

Curr Protoc. 2025 Feb;5(2):e70109. doi: 10.1002/cpz1.70109.

Abstract

Mice carrying patient-associated base changes are powerful tools to define the causality of single-nucleotide variants to disease states. Epitope tags enable immuno-based studies of genes for which no antibodies are available. These alleles enable detailed and precise developmental, mechanistic, and translational research. The first step in generating these alleles is to identify within the target sequence-the orthologous sequence for base changes or the N or C terminus for epitope tags-appropriate Cas9 protospacer sequences. Subsequent steps include design and acquisition of a single-stranded oligonucleotide repair template, synthesis of a single guide RNA (sgRNA), collection of zygotes, and microinjection or electroporation of zygotes with Cas9 mRNA or protein, sgRNA, and repair template followed by screening born mice for the presence of the desired sequence change. Quality control of mouse lines includes screening for random or multicopy insertions of the repair template and, depending on sgRNA sequence, off-target sequence variation introduced by Cas9. © 2025 The Author(s). Current Protocols published by Wiley Periodicals LLC. Basic Protocol 1: Single guide RNA design and synthesis Alternate Protocol 1: Single guide RNA synthesis by primer extension and in vitro transcription Basic Protocol 2: Design of oligonucleotide repair template Basic Protocol 3: Preparation of RNA mixture for microinjection Support Protocol 1: Preparation of microinjection buffer Alternate Protocol 2: Preparation of RNP complexes for electroporation Basic Protocol 4: Collection and preparation of mouse zygotes for microinjection or electroporation Basic Protocol 5: Electroporation of Cas9 RNP into zygotes using cuvettes Alternate Protocol 3: Electroporation of Cas9 RNP into zygotes using electrode slides Basic Protocol 6: Screening and quality control of derived mice Support Protocol 2: Deconvoluting multiple sequence chromatograms with DECODR.

摘要

携带患者相关碱基变化的小鼠是确定单核苷酸变体与疾病状态因果关系的有力工具。表位标签可用于对没有可用抗体的基因进行基于免疫的研究。这些等位基因有助于进行详细而精确的发育、机制和转化研究。生成这些等位基因的第一步是在靶序列内确定合适的Cas9原间隔序列,对于碱基变化而言是直系同源序列,对于表位标签而言是N端或C端。后续步骤包括设计和获取单链寡核苷酸修复模板、合成单向导RNA(sgRNA)、收集受精卵,并用Cas9 mRNA或蛋白质、sgRNA和修复模板对受精卵进行显微注射或电穿孔,然后筛选出生小鼠中是否存在所需的序列变化。小鼠品系的质量控制包括筛选修复模板的随机或多拷贝插入,以及根据sgRNA序列筛选Cas9引入的脱靶序列变异。© 2025作者。由Wiley Periodicals LLC出版的《当前实验方案》。基本方案1:单向导RNA的设计与合成 替代方案1:通过引物延伸和体外转录合成单向导RNA 基本方案2:寡核苷酸修复模板的设计 基本方案3:用于显微注射的RNA混合物的制备 支持方案1:显微注射缓冲液的制备 替代方案2:用于电穿孔的核糖核蛋白复合物的制备 基本方案4:用于显微注射或电穿孔的小鼠受精卵的收集和制备 基本方案5:使用比色杯将Cas9核糖核蛋白电穿孔到受精卵中 替代方案3:使用电极载玻片将Cas9核糖核蛋白电穿孔到受精卵中 基本方案6:衍生小鼠的筛选和质量控制 支持方案2:使用DECODR对多个序列色谱图进行解卷积分析

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e05/11856344/c47c23a22f73/CPZ1-5-0-g002.jpg

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