Development of an endogenous promoter-driven CRISPR/Cas9 system for genome editing in <i>Fraxinus mandshurica</i>

CRISPR/Cas9-mediated genome editing has revolutionized tree improvement by enabling precise trait modification, accelerating breeding cycles, and enhancing forestry sustainability. <i>Fraxinus mandshurica</i>, valued for its desirable traits and adaptability, serves as a strategic focus for the National Reserve Forest Project (NRFP) and forestry germplasm resource breeding and quality improvement in China. Developing a species-specific genome editing system is crucial for valuable yet recalcitrant species like <i>F. mandshurica</i>. In this study, the development of a species-specific CRISPR/Cas9 platform is presented for <i>F. mandshurica</i>, which incorporates endogenous promoter engineering, sgRNA optimization, light quality modulation, and temperature control protocols to enhance genome editing efficiency. Truncated endogenous <i>FmU6</i> promoter variants (<i>FmU6-6-4</i> and <i>FmU6-7-4</i>) drove sgRNA expression at levels 3.36 and 3.11 times higher than that of the <i>AtU6-26</i> promoter. The expression of Cas9 was controlled by the endogenous constitutive <i>FmECP3</i> promoter, exhibiting an activity 5.48 times greater than the positive control. A highly active sgRNA4 targeting <i>FmPDS1/2</i> was identified, demonstrating a cleavage efficiency of 36.10%. Heat treatment at 37 °C effectively increased the Cas9 cleavage efficiency to 7.77 times that observed at 22 °C. Chimeric albino mutants with an editing efficiency of 18.2% were obtained through transient and stable transformations, combined with light quality optimization and heat treatment during different regeneration stages. The mutation types included nucleotide insertions, deletions, and substitutions, leading to early termination codons and truncated FmPDS1/2 protein. Additionally, mutations in <i>FmPDS1/2</i> resulted in albino phenotypes and a reduction in chlorophyll content to 46.44%-58.88%. This optimized system provides a robust platform for functional genomics studies and trait improvement in <i>F. mandshurica</i>, with potential applications in forestry biotechnology.

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Publication Details

Journal
Forestry Research
Published
2025-01-01
DOI
https://doi.org/10.48130/forres-0025-0016
Citations
1
Primary Topic
CRISPR and Genetic Engineering
Type
article
Field-Weighted Citation Impact
0.81
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article

Development of an endogenous promoter-driven CRISPR/Cas9 system for genome editing in Fraxinus mandshurica

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1 citations
Forestry Research
CRISPR and Genetic Engineering
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article

Development of an endogenous promoter-driven CRISPR/Cas9 system for genome editing in Fraxinus mandshurica

Jinyue Yan, Mingwen Zhao, Siyu Sun, Shangzhu Gao, Xing Fan, Ying Xin, Fansuo Zeng, Yaguang Zhan
article en
1 citations

Abstract

CRISPR/Cas9-mediated genome editing has revolutionized tree improvement by enabling precise trait modification, accelerating breeding cycles, and enhancing forestry sustainability. <i>Fraxinus mandshurica</i>, valued for its desirable traits and adaptability, serves as a strategic focus for the National Reserve Forest Project (NRFP) and forestry germplasm resource breeding and quality improvement in China. Developing a species-specific genome editing system is crucial for valuable yet recalcitrant species like <i>F. mandshurica</i>. In this study, the development of a species-specific CRISPR/Cas9 platform is presented for <i>F. mandshurica</i>, which incorporates endogenous promoter engineering, sgRNA optimization, light quality modulation, and temperature control protocols to enhance genome editing efficiency. Truncated endogenous <i>FmU6</i> promoter variants (<i>FmU6-6-4</i> and <i>FmU6-7-4</i>) drove sgRNA expression at levels 3.36 and 3.11 times higher than that of the <i>AtU6-26</i> promoter. The expression of Cas9 was controlled by the endogenous constitutive <i>FmECP3</i> promoter, exhibiting an activity 5.48 times greater than the positive control. A highly active sgRNA4 targeting <i>FmPDS1/2</i> was identified, demonstrating a cleavage efficiency of 36.10%. Heat treatment at 37 °C effectively increased the Cas9 cleavage efficiency to 7.77 times that observed at 22 °C. Chimeric albino mutants with an editing efficiency of 18.2% were obtained through transient and stable transformations, combined with light quality optimization and heat treatment during different regeneration stages. The mutation types included nucleotide insertions, deletions, and substitutions, leading to early termination codons and truncated FmPDS1/2 protein. Additionally, mutations in <i>FmPDS1/2</i> resulted in albino phenotypes and a reduction in chlorophyll content to 46.44%-58.88%. This optimized system provides a robust platform for functional genomics studies and trait improvement in <i>F. mandshurica</i>, with potential applications in forestry biotechnology.

Forestry ResearchVol. 5(1)
Northeast Forestry University (CN)
Openalex Percentile: Top 25%
CRISPR and Genetic Engineering
0.81
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