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Volume 43 Issue 1
Jan.  2016
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Article Contents

Efficiency and Inheritance of Targeted Mutagenesis in Maize Using CRISPR-Cas9

doi: 10.1016/j.jgg.2015.10.006
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  • Corresponding author: E-mail address: jlai@cau.edu.cn (Jinsheng Lai)
  • Received Date: 2015-09-30
  • Revised Date: 2015-10-27
  • Accepted Date: 2015-10-29
  • Available Online: 2015-12-21
  • Publish Date: 2016-01-20
  • CRISPR/Cas (clustered regularly interspaced short palindromic repeats/CRISPR-associated proteins) is an adaptive immune system in bacteria and archaea to defend against invasion from foreign DNA fragments. Recently, it has been developed as a powerful targeted genome editing tool for a wide variety of species. However, its application in maize has only been tested with transiently expressed somatic cells or with a limited number of stable transgenic T0 plants. The exact efficiency and specificity of the CRISPR/Cas system in the highly complex maize genome has not been documented yet. Here we report an extensive study of the well-studied type II CRISPR-Cas9 system for targeted genome editing in maize, with the codon-optimized Cas9 protein and the short non-coding guide RNA generated through a functional maize U6 snRNA promoter. Targeted gene mutagenesis was detected for 90 loci by maize protoplast assay, with an average cleavage efficiency of 10.67%. Stable knockout transformants for maize phytoene synthase gene (PSY1) were obtained. Mutations occurred in germ cells can be stably inherited to the next generation. Moreover, no off-target effect was detected at the computationally predicted putative off-target loci. No significant difference between the transcriptomes of the Cas9 expressed and non-expressed lines was detected. Our results confirmed that the CRISPR-Cas9 could be successfully applied as a robust targeted genome editing system in maize.
  • These authors contributed equally to this work.
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