A simple, quick, and efficient CRISPR/Cas9 genome editing method for human induced pluripotent stem cells
Autor: | Hua Zhu, Nian-guo Dong, Bingchuan Geng, Jae-Kyun Ko, Peng Chen, Shanzhi Wang, Xiu-di Pan, Kyoung-Han Choi |
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Rok vydání: | 2020 |
Předmět: |
0301 basic medicine
Induced Pluripotent Stem Cells Pharmacology toxicology Computational biology Biology Article Gene Knockout Techniques 03 medical and health sciences 0302 clinical medicine Plasmid Genome editing CRISPR-Associated Protein 9 Humans CRISPR Pharmacology (medical) Human Induced Pluripotent Stem Cells Induced pluripotent stem cell Gene Gene Editing Pharmacology Base Sequence Cas9 Cell Differentiation General Medicine 030104 developmental biology 030220 oncology & carcinogenesis CRISPR-Cas Systems Ubiquitin Thiolesterase Plasmids |
Zdroj: | Acta Pharmacol Sin |
ISSN: | 1745-7254 1671-4083 |
DOI: | 10.1038/s41401-020-0452-0 |
Popis: | Induced pluripotent stem cells (iPSCs) have become an essential research platform to study different human diseases once being discovered by Dr. Shinya Yamanaka in 2006. Another breakthrough in biomedical research is the application of CRISPR/Cas9 system for genome editing in mammalian cells. Although numerous studies have been done to develop methods for gene editing in iPSCs, the current approaches suffer from several limitations, including time and labor consuming, low editing efficiency, and potential off-target effects. In the current study, we report an electroporation-mediated plasmid CRISPR/Cas9 delivery approach for genome editing in iPSCs. With this approach, an edited iPSC cell line could be obtained within 2 weeks. In addition, the transit introducing of CRISPR/Cas9 machinery could minimize genomic integration of Cas9 gene, which avoided potential long-term side effects of Cas9 enzyme. We showed that CRISPR/Cas9-mediated genomic editing did not affect pluripotency and differentiation ability of iPSCs. With the quickly evolving of both iPSC and CRISPR/Cas9-mediated genome editing research fields, we believe that our method can significantly facilitate the application of genome editing in iPSCs research. |
Databáze: | OpenAIRE |
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