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Review
. 2015 Dec;13(6):336-44.
doi: 10.1016/j.gpb.2015.12.001. Epub 2016 Jan 4.

Genome Editing and Its Applications in Model Organisms

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Review

Genome Editing and Its Applications in Model Organisms

Dongyuan Ma et al. Genomics Proteomics Bioinformatics. 2015 Dec.

Abstract

Technological advances are important for innovative biological research. Development of molecular tools for DNA manipulation, such as zinc finger nucleases (ZFNs), transcription activator-like effector nucleases (TALENs), and the clustered regularly-interspaced short palindromic repeat (CRISPR)/CRISPR-associated (Cas), has revolutionized genome editing. These approaches can be used to develop potential therapeutic strategies to effectively treat heritable diseases. In the last few years, substantial progress has been made in CRISPR/Cas technology, including technical improvements and wide application in many model systems. This review describes recent advancements in genome editing with a particular focus on CRISPR/Cas, covering the underlying principles, technological optimization, and its application in zebrafish and other model organisms, disease modeling, and gene therapy used for personalized medicine.

Keywords: CRISPR/Cas; Disease model; Gene therapy; Genome editing; Zebrafish.

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Figures

Figure 1
Figure 1
The timeline for applications of CRISPR/Cas technology in model organisms
Figure 2
Figure 2
CRISPR/Cas in zebrafish

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References

    1. Travis J. Making the cut. Science. 2015;350:1456–1457. - PubMed
    1. Bibikova M., Beumer K., Trautman J.K., Carroll D. Enhancing gene targeting with designed zinc finger nucleases. Science. 2003;300:764. - PubMed
    1. Bibikova M., Golic M., Golic K.G., Carroll D. Targeted chromosomal cleavage and mutagenesis in Drosophila using zinc-finger nucleases. Genetics. 2002;161:1169–1175. - PMC - PubMed
    1. Kim Y.G., Cha J., Chandrasegaran S. Hybrid restriction enzymes: zinc finger fusions to Fok I cleavage domain. Proc Natl Acad Sci U S A. 1996;93:1156–1160. - PMC - PubMed
    1. Strobel S.A., Dervan P.B. Site-specific cleavage of a yeast chromosome by oligonucleotide-directed triple-helix formation. Science. 1990;249:73–75. - PubMed

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