Genentech, Inc., Department of Molecular Biology, South San Francisco, CA, USA.
Methods Mol Biol. 2023;2631:135-153. doi: 10.1007/978-1-0716-2990-1_5.
Generation of transgenic mice by direct microinjection of foreign DNA into fertilized ova has become a routine technique in biomedical research. It remains an essential tool for studying gene expression, developmental biology, genetic disease models, and their therapies. However, the random integration of foreign DNA into the host genome that is inherent to this technology can lead to confounding effects associated with insertional mutagenesis and transgene silencing. Locations of most transgenic lines remain unknown because the methods are often burdensome (Nicholls et al., G3: Genes Genomes Genetics 9:1481-1486, 2019) or have limitations (Goodwin et al., Genome Research 29:494-505, 2019). Here, we present a method that we call Adaptive Sampling Insertion Site Sequencing (ASIS-Seq) to locate transgene integration sites using targeted sequencing on Oxford Nanopore Technologies' (ONT) sequencers. ASIS-Seq requires only about 3 ug of genomic DNA, 3 hours of hands-on sample preparation time, and 3 days of sequencing time to locate transgenes in a host genome.
通过将外源 DNA 直接微注射到受精卵中生成转基因小鼠已成为生物医学研究中的常规技术。它仍然是研究基因表达、发育生物学、遗传疾病模型及其治疗方法的重要工具。然而,该技术中外源 DNA 随机整合到宿主基因组中会导致与插入诱变和转基因沉默相关的混杂效应。由于方法通常繁琐(Nicholls 等人,G3:基因、基因组、遗传学 9:1481-1486, 2019)或具有局限性(Goodwin 等人,基因组研究 29:494-505, 2019),大多数转基因系的位置仍然未知。在这里,我们提出了一种称为适应性采样插入位点测序(ASIS-Seq)的方法,该方法使用靶向测序在 Oxford Nanopore Technologies(ONT)测序仪上定位转基因整合位点。ASIS-Seq 仅需要约 3μg 的基因组 DNA、3 小时的手动样本制备时间和 3 天的测序时间即可定位宿主基因组中的转基因。