| Literature DB >> 29542087 |
Shashank Gandhi1, Florian Razy-Krajka2, Lionel Christiaen3, Alberto Stolfi4.
Abstract
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.Entities:
Keywords: Chordates; Genome editing; Somatic gene knockout; Targeted mutagenesis; Tunicates; sgRNAs
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Year: 2018 PMID: 29542087 PMCID: PMC6061950 DOI: 10.1007/978-981-10-7545-2_13
Source DB: PubMed Journal: Adv Exp Med Biol ISSN: 0065-2598 Impact factor: 2.622