Department of Respiratory and Critical Care Medicine, The Center for Biomedical Research, NHC Key Laboratory of Respiratory Diseases, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei Province, China.
Department of Pharmacy, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Hubei Province, Wuhan, China.
Mol Biotechnol. 2022 Nov;64(11):1227-1233. doi: 10.1007/s12033-022-00500-5. Epub 2022 May 3.
With the development of CRISPR-Cas9 gene editing and in vitro fertilization (IVF) technology, we can now easily construct genetically modified mouse strains with indels, especially for loxP-based strategy. However, the general genotyping methods are time-consuming and unreliable given the loxP site is only 34 bp long. Here, based on the tetra primer-paired PCR amplification, we describe an efficient genotyping method which can simultaneously generate the internal control band, wild type (wt)-genotype band, and/or loxP-genotype band through one single PCR amplification. It is easy to interpret the mouse genotypes from the pattern of the bands. Further, the results could also help to exclude the possibility of minor cross-contamination, since the ratio between the bands' quantity in wt/wt, wt/loxP, and loxP/loxP mice are relatively constant, which makes the genotyping more reliable when it is performed in a large amount.
随着 CRISPR-Cas9 基因编辑和体外受精 (IVF) 技术的发展,我们现在可以轻松构建具有缺失和插入的基因修饰小鼠品系,特别是基于 loxP 的策略。然而,由于 loxP 位点只有 34 个碱基长,一般的基因分型方法既耗时又不可靠。在这里,我们基于四引物配对 PCR 扩增,描述了一种高效的基因分型方法,该方法可以通过单次 PCR 扩增同时产生内对照带、野生型 (wt)-基因型带和/或 loxP-基因型带。从条带的模式很容易解释小鼠的基因型。此外,由于 wt/wt、wt/loxP 和 loxP/loxP 小鼠中条带数量之间的比例相对恒定,因此当大量进行时,该结果还可以帮助排除微小交叉污染的可能性,从而使基因分型更加可靠。