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Front Genet. 2018 Jul 5;9:240. doi: 10.3389/fgene.2018.00240. eCollection 2018.

CRISPR/Cascade 9-Mediated Genome Editing-Challenges and Opportunities.

Author information

1
BGI Genomics, BGI-Shenzhen, Shenzhen, China.
2
Laboratory of Genomics and Molecular Biomedicine, Department of Biology, University of Copenhagen, Copenhagen, Denmark.
3
School of Life Sciences, Tsinghua University, Beijing, China.
4
Institute of Sericulture and Apiculture, College of Animal Sciences, Zhejiang University, Hangzhou, China.
5
Institute of Marine Research, Bergen, Norway.

Abstract

Clustered Regularly Interspaced Palindromic Repeats (CRISPR) and Cascade 9 (also known as Cas9, CRISPR associated protein 9) confer protection against invading viruses or plasmids. The CRISPR/Cascade 9 system constitutes one of the most powerful genome technologies available to researchers today. So far, this technology has enabled efficient genome editing and modification in several model organisms and has successfully been used in biomedicine and biomedical engineering. However, challenges for efficient and safe genetic manipulation in several organisms persist. Here, we review functional approaches and future challenges associated with the use of the CRISPR/Cascade 9 genome editing system and discuss opportunities, ethical issues and future directions within this field.

KEYWORDS:

CRISPR; Cascade 9; RNA guided system; gene targeting; genome editing; off-target effects

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