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Screening Methods to Identify TALEN-Mediated Knockout Mice

机译:筛选TALEN介导的基因敲除小鼠的筛选方法

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Genome editing with site-specific nucleases, such as zinc-finger nucleases or transcription activator-like effector nucleases (TALENs), and RNA-guided nucleases, such as the CRISPR/Cas (clustered regularly interspaced short palindromic repeats/CRISPR-associated) system, is becoming the new standard for targeted genome modification in various organisms. Application of these techniques to the manufacture of knockout mice would be greatly aided by simple and easy methods for genotyping of mutant and wild-type pups among litters. However, there are no detailed or comparative reports concerning the identification of mutant mice generated using genome editing technologies. Here, we genotyped TALEN-derived enhanced green fluorescent protein ( eGFP ) knockout mice using a combination of approaches, including fluorescence observation, heteroduplex mobility assay, restriction fragment length polymorphism analysis and DNA sequencing. The detection sensitivities for TALEN-induced mutations differed among these methods, and we therefore concluded that combinatorial testing is necessary for the screening and determination of mutant genotypes. Since the analytical methods tested can be carried out without specialized equipment, costly reagents and/or sophisticated protocols, our report should be of interest to a broad range of researchers who are considering the application of genome editing technologies in various organisms.
机译:使用位点特异性核酸酶(例如锌指核酸酶或转录激活因子样效应子核酸酶(TALENs))和RNA引导的核酸酶(例如CRISPR / Cas(聚簇的规则间隔的短回文重复序列/ CRISPR相关)系统)进行基因组编辑成为各种生物中靶向基因组修饰的新标准。将这些技术应用于基因敲除小鼠的生产将通过简单易行的方法对产仔中的突变和野生型幼仔进行基因分型而大大帮助。但是,没有有关使用基因组编辑技术生成的突变小鼠的鉴定的详细或比较报告。在这里,我们使用包括荧光观察,异源双链迁移分析,限制性片段长度多态性分析和DNA测序在内的多种方法对TALEN衍生的增强型绿色荧光蛋白(eGFP)敲除小鼠进行了基因分型。这些方法对TALEN诱导的突变的检测敏感性不同,因此我们得出结论,组合测试对于筛选和确定突变基因型是必要的。由于所测试的分析方法无需专门的设备,昂贵的试剂和/或复杂的规程即可进行,我们的报告应引起正在考虑将基因组编辑技术应用于各种生物的广泛研究人员的关注。

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