Genome editing in maize directed by CRISPR–Cas9 ribonucleoprotein complexes

By S. Svitashev, C. Schwartz, B. Lenderts, Joshua K. Young, A. Mark Cigan. Nature Communications, 2016

696 citations recorded by the source corpus.

Targeted DNA double-strand breaks have been shown to significantly increase the frequency and precision of genome editing. In the past two decades, several double-strand break technologies have been developed. CRISPR–Cas9 has quickly become the technology of choice for genome editing due to its simplicity, efficiency and versatility. Currently, genome editing in plants primarily relies on delivering double-strand break reagents in the form of DNA vectors. Here we report biolistic delivery of pre-assembled Cas9–gRNA ribonucleoproteins into maize embryo cells and regeneration of plants with both mutated and edited alleles. Using this method of delivery, we also demonstrate DNA- and selectable marker-free gene mutagenesis in maize and recovery of plants with mutated alleles at high frequencies. These results open new opportunities to accelerate breeding practices in a wide variety of crop species. Genome editing in plants typically requires the expression of Cas9 and guide RNA from stably transformed plasmid DNA. Here, the authors show that successful editing can be achieved after delivery of the Cas9-guide RNA complex as a ribonucleoprotein to maize embryos via biolistics.

Subfields: Insect Science, Molecular Biology, Plant Science

View Paper: https://www.semanticscholar.org/paper/27b11b05901ef1ff4113cc7cc2e913320787bd3d

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In Insect Science

  1. Caixia Gao
  2. Jian‐Kang Zhu

In Molecular Biology

  1. Caixia Gao
  2. Kunling Chen
  3. Yanpeng Wang
  4. Jian‐Kang Zhu

In Plant Science

  1. Caixia Gao
  2. Kunling Chen
  3. Yanpeng Wang
  4. Jian‐Kang Zhu
  5. M. Ashraf
  6. Kazuko Yamaguchi-Shinozaki
  7. Kazuo Shinozaki
  8. Viswanathan Chinnusamy

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