Paix Alexandre, Folkmann Andrew, Seydoux Geraldine
Dept of Molecular Biology and Genetics, Johns Hopkins University, School of Medicine, 725 N. Wolfe Street, Baltimore, MD 21205, USA.
Dept of Molecular Biology and Genetics, Johns Hopkins University, School of Medicine, 725 N. Wolfe Street, Baltimore, MD 21205, USA.
Methods. 2017 May 15;121-122:86-93. doi: 10.1016/j.ymeth.2017.03.023. Epub 2017 Apr 7.
The ability to introduce targeted edits in the genome of model organisms is revolutionizing the field of genetics. State-of-the-art methods for precision genome editing use RNA-guided endonucleases to create double-strand breaks (DSBs) and DNA templates containing the edits to repair the DSBs. Following this strategy, we have developed a protocol to create precise edits in the C. elegans genome. The protocol takes advantage of two innovations to improve editing efficiency: direct injection of CRISPR-Cas9 ribonucleoprotein complexes and use of linear DNAs with short homology arms as repair templates. The protocol requires no cloning or selection, and can be used to generate base and gene-size edits in just 4days. Point mutations, insertions, deletions and gene replacements can all be created using the same experimental pipeline.
在模式生物基因组中引入靶向编辑的能力正在彻底改变遗传学领域。最先进的精确基因组编辑方法使用RNA引导的核酸内切酶来产生双链断裂(DSB),并利用包含编辑内容的DNA模板来修复DSB。按照这一策略,我们开发了一种在秀丽隐杆线虫基因组中进行精确编辑的方案。该方案利用两项创新来提高编辑效率:直接注射CRISPR-Cas9核糖核蛋白复合物,以及使用具有短同源臂的线性DNA作为修复模板。该方案无需克隆或筛选,仅需4天即可用于产生碱基和基因大小的编辑。点突变、插入、缺失和基因替换均可使用相同的实验流程来创建。