Center for Developmental Genetics, Department of Biology, New York University, New York, NY, USA.
Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, USA.
Adv Exp Med Biol. 2018;1029:141-152. doi: 10.1007/978-981-10-7545-2_13.
Clustered regularly interspaced short palindromic repeats (CRISPR)/Cas9 has emerged as a revolutionary tool for fast and efficient targeted gene knockouts and genome editing in almost any organism. The laboratory model tunicate Ciona is no exception. Here, we describe our latest protocol for the design, implementation, and evaluation of successful CRISPR/Cas9-mediated gene knockouts in somatic cells of electroporated Ciona embryos. Using commercially available reagents, publicly accessible plasmids, and free web-based software applications, any Ciona researcher can easily knock out any gene of interest in their favorite embryonic cell lineage.
成簇规律间隔短回文重复序列 (CRISPR)/Cas9 已成为在几乎任何生物体中快速、高效靶向基因敲除和基因组编辑的革命性工具。实验室模型海鞘也不例外。在这里,我们描述了我们最新的设计、实施和评估 CRISPR/Cas9 介导的体细胞基因敲除的方案,该方案在电穿孔的海鞘胚胎中使用。通过使用商业上可获得的试剂、可公开访问的质粒和免费的基于网络的软件应用程序,任何海鞘研究人员都可以轻松地敲除其感兴趣的胚胎细胞谱系中的任何基因。