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Pollen-Specific CRISPR/Cas9 System to Increase Heritable Gene Mutations in Maize

Author

Listed:
  • Changshuang Jing

    (Shanghai Key Laboratory of Bio-Energy Crops, School of Life Sciences, Shanghai University, Shanghai 200444, China)

  • Min Wei

    (Shanghai Key Laboratory of Bio-Energy Crops, School of Life Sciences, Shanghai University, Shanghai 200444, China)

  • Peng Fang

    (Shanghai Key Laboratory of Bio-Energy Crops, School of Life Sciences, Shanghai University, Shanghai 200444, China)

  • Rentao Song

    (State Key Laboratory of Plant Physiology and Biochemistry, National Maize Improvement Center, College of Agronomy and Biotechnology, China Agricultural University, Beijing 100193, China
    Beijing Key Laboratory of Crop Genetic Improvement, College of Agronomy and Biotechnology, China Agricultural University, Beijing 100193, China
    Joint International Research Laboratory of Crop Molecular Breeding, College of Agronomy and Biotechnology, China Agricultural University, Beijing 100193, China)

  • Weiwei Qi

    (Shanghai Key Laboratory of Bio-Energy Crops, School of Life Sciences, Shanghai University, Shanghai 200444, China)

Abstract

The CRISPR/Cas9 system has been widely utilized in plant biotechnology as a gene editing tool. However, a conventional design with ubiquitously expressed CRISPR/Cas9 was observed to cause large numbers of somatic mutations that complicated the identification of heritable mutations. We constructed a pollen-specific CRISPR/Cas9 (PSC) system using pollen-specific promoters of maize Profilin 1 and Profilin 3 (pZmPRO1 and pZmPRO3) to drive Cas9 expression, and the bZIP transcription factor Opaque2 ( O2 ) was employed as the target gene. The maize ubiquitin promoter (pZmUbi)-driven CRISPR/Cas9 (UC) system was employed as a control. We generated transgenic plants for the PSC and UC systems and analyzed three independent events for each system. We found that the pZmPRO1 PSC system generated no target gene mutations in the T0 generation but successfully generated 0–90% target gene mutations in the T1 generation. A total of 31 of 33 mutations in the T1 generation could be inherited in the T2 generation. In addition, 88.9–97.3% of T2 mutations were from the T1 generation. The UC system generated mutations in the T0 generation, and 0%, 50% and 92.9% of T1 mutations were from the T0 generation. Our results demonstrate that the PSC system provided stable, heritable mutants in the next generation, and this approach might also be applied in other crops using germinal cell-specific CRISPR/Cas9 systems to facilitate plant breeding.

Suggested Citation

  • Changshuang Jing & Min Wei & Peng Fang & Rentao Song & Weiwei Qi, 2021. "Pollen-Specific CRISPR/Cas9 System to Increase Heritable Gene Mutations in Maize," Agriculture, MDPI, vol. 11(8), pages 1-10, August.
  • Handle: RePEc:gam:jagris:v:11:y:2021:i:8:p:751-:d:610091
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    References listed on IDEAS

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    1. Blake Wiedenheft & Samuel H. Sternberg & Jennifer A. Doudna, 2012. "RNA-guided genetic silencing systems in bacteria and archaea," Nature, Nature, vol. 482(7385), pages 331-338, February.
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