内源性启动子驱动的水曲霉基因组编辑CRISPR/Cas9系统的建立

IF 5
Forestry research Pub Date : 2025-08-04 eCollection Date: 2025-01-01 DOI:10.48130/forres-0025-0016
Shangzhu Gao, Mengfan Zhao, Siyu Sun, Xin Fan, Jialin Yan, Ying Xin, Yaguang Zhan, Fansuo Zeng
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引用次数: 0

摘要

CRISPR/ cas9介导的基因组编辑通过实现精确的性状修饰、加速育种周期和增强林业可持续性,彻底改变了树木的改良。水曲柳(Fraxinus manshurica)因其优良的性状和适应性而受到重视,是中国国家级保护林工程(NRFP)和林业种质资源育种和质量改良的战略重点。开发一种物种特异性的基因组编辑系统对于像水曲柳这样有价值但又难治性的物种至关重要。本研究提出了一种针对水曲霉的物种特异性CRISPR/Cas9平台的开发,该平台结合了内源启动子工程、sgRNA优化、光质量调制和温度控制协议,以提高基因组编辑效率。截断的内源性FmU6启动子变体(FmU6-6-4和FmU6-7-4)驱动sgRNA的表达水平分别是AtU6-26启动子的3.36倍和3.11倍。Cas9的表达受内源性组成型FmECP3启动子的控制,其活性是阳性对照的5.48倍。在FmPDS1/2上发现了一个高活性的sgRNA4,裂解效率为36.10%。37℃热处理能有效提高Cas9的裂解效率,达到22℃时的7.77倍。通过瞬时稳定转化,结合不同再生阶段的光质量优化和热处理,获得了编辑效率为18.2%的嵌合白化突变体。突变类型包括核苷酸插入、缺失和替换,导致早期终止密码子和截断FmPDS1/2蛋白。此外,FmPDS1/2突变导致白化表型,叶绿素含量降低至46.44%-58.88%。该系统为水曲柳的功能基因组学研究和性状改良提供了强有力的平台,在林业生物技术方面具有潜在的应用前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of an endogenous promoter-driven CRISPR/Cas9 system for genome editing in Fraxinus mandshurica.

CRISPR/Cas9-mediated genome editing has revolutionized tree improvement by enabling precise trait modification, accelerating breeding cycles, and enhancing forestry sustainability. Fraxinus mandshurica, 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 F. mandshurica. In this study, the development of a species-specific CRISPR/Cas9 platform is presented for F. mandshurica, which incorporates endogenous promoter engineering, sgRNA optimization, light quality modulation, and temperature control protocols to enhance genome editing efficiency. Truncated endogenous FmU6 promoter variants (FmU6-6-4 and FmU6-7-4) drove sgRNA expression at levels 3.36 and 3.11 times higher than that of the AtU6-26 promoter. The expression of Cas9 was controlled by the endogenous constitutive FmECP3 promoter, exhibiting an activity 5.48 times greater than the positive control. A highly active sgRNA4 targeting FmPDS1/2 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 FmPDS1/2 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 F. mandshurica, with potential applications in forestry biotechnology.

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