Wang Chunming, Sun Chao, Shi Li, Zhou Jiannan, Liu Shuai, Bai Yongsheng, Yu Weichang
Guangdong Key Laboratory of Plant Epigenetics, College of Life Sciences and Oceanography, Shenzhen University, Shenzhen, China.
Shenzhen Academy of Metrology and Quality Inspection, Shenzhen, China.
CRISPR J. 2025 Feb;8(1):51-59. doi: 10.1089/crispr.2024.0064. Epub 2025 Jan 13.
Flax is an important crop used for oil and fiber production. Although genetic engineering has been possible in flax, it is not commonly used to produce cultivars. However, the use of genome editing technology, which can produce site-specific mutations without introducing foreign genes, may be a valuable tool for creating elite cultivars that can be easily cultivated. The purpose of this study was to investigate the potential of genome editing in flax by establishing the clustered regularly interspaced short palindromic repeats (CR ISPR)-CRISPR-associated protein 9 (CRISPR-Cas9) genome editing system using the phytoene desaturase () gene, which produces albino mutants that are easily identifiable. Four sgRNAs were designed from two genes of Flax (LuPDS1 and LuPDS2), and CRISPR-Cas9 genome editing vectors were constructed. After gene transformation, albino phenotypes were observed in transformed callus and regenerated plantlets on selection media. Polymerase chain reaction (PCR) amplification and sequencing of the genes revealed deletions and insertions in the albino tissues, indicating successful editing of the genes. Potential off-target sites were analyzed, but no off-target mutations were found, indicating the specificity of the CRISPR-Cas9 system. The establishment of a flax genome editing system using the CRISPR-Cas9 technology opens up new possibilities for the genetic engineering of flax. This study demonstrates the potential of genome editing in creating elite cultivars that can be easily cultivated, which can have significant implications for the flax industry.
亚麻是一种用于生产油和纤维的重要作物。虽然亚麻的基因工程是可行的,但它并不常用于培育品种。然而,基因组编辑技术能够产生位点特异性突变而不引入外源基因,可能是培育易于栽培的优良品种的宝贵工具。本研究的目的是通过利用八氢番茄红素去饱和酶()基因建立成簇规律间隔短回文重复序列(CRISPR)-CRISPR相关蛋白9(CRISPR-Cas9)基因组编辑系统,来研究亚麻基因组编辑的潜力,该基因会产生易于识别的白化突变体。从亚麻的两个基因(LuPDS1和LuPDS2)设计了4个单向导RNA,并构建了CRISPR-Cas9基因组编辑载体。基因转化后,在选择培养基上的转化愈伤组织和再生小植株中观察到白化表型。对基因进行聚合酶链反应(PCR)扩增和测序,发现在白化组织中有缺失和插入,表明基因编辑成功。对潜在的脱靶位点进行了分析,但未发现脱靶突变,表明CRISPR-Cas9系统具有特异性。利用CRISPR-Cas9技术建立亚麻基因组编辑系统为亚麻的基因工程开辟了新的可能性。本研究证明了基因组编辑在培育易于栽培的优良品种方面的潜力,这可能对亚麻产业产生重大影响。