4.6 Article

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

Journal

PLOS ONE
Volume 8, Issue 7, Pages -

Publisher

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pone.0068708

Keywords

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Funding

  1. National Institutes of Health [R01 GM088040]
  2. NIH Director's Pioneer Award [DP1 OD006862, K01 AG031300, R01 CA140188]
  3. Defense Advanced Research Projects Agency (DARPA) [W911NF-11-2-0056]
  4. Jim and Ann Orr MGH Research Scholar award
  5. Charles and Ann Sanders MGH Research Scholar award
  6. MGH Claflin Distinguished Scholar Award

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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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