Heritable and Precise Zebrafish Genome Editing Using a CRISPR-Cas System

Woong Y. Hwang(Harvard University), Yanfang Fu(Center for Cancer Research), Deepak Reyon(Harvard University), Morgan L. Maeder(Massachusetts General Hospital), Prakriti Kaini(Massachusetts General Hospital), Jeffry D. Sander(Harvard University), J. Keith Joung(Massachusetts General Hospital), Randall T. Peterson(Broad Institute), Jing-Ruey Joanna Yeh(Harvard University)
PLoS ONE
July 9, 2013
Cited by 376Open Access
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Abstract

We have previously reported a simple and customizable CRISPR (clustered regularly interspaced short palindromic repeats) RNA-guided Cas9 nuclease (RGN) system that can be used to efficiently and robustly introduce somatic indel mutations in endogenous zebrafish genes. Here we demonstrate that RGN-induced mutations are heritable, with efficiencies of germline transmission reaching as high as 100%. In addition, we extend the power of the RGN system by showing that these nucleases can be used with single-stranded oligodeoxynucleotides (ssODNs) to create precise intended sequence modifications, including single nucleotide substitutions. Finally, we describe and validate simple strategies that improve the targeting range of RGNs from 1 in every 128 basepairs (bps) of random DNA sequence to 1 in every 8 bps. Together, these advances expand the utility of the CRISPR-Cas system in the zebrafish beyond somatic indel formation to heritable and precise genome modifications.


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