Wu Ruqian, Chai Yinghui, Li Ying, Chen Tingting, Qi Wanxin, Xue Yinxuan, Lu Hailin, Chen Zhong, Guo Bin, Li Shanwen, Qin Debin, An Xinmin
State Key Laboratory of Tree Genetics and Breeding, College of Biological Sciences and Technology, Beijing Forestry University, Beijing, China.
National Engineering Research Center of Tree Breeding and Ecological Restoration, College of Biological Sciences and Technology, Beijing Forestry University, Beijing, China.
Plant Biotechnol J. 2025 Sep;23(9):4017-4029. doi: 10.1111/pbi.70219. Epub 2025 Jun 20.
The CRISPR-Cas9 system has emerged as a potent molecular scalpel for precise genome editing, and profoundly revolutionized plant genetics and breeding, facilitating the development of innovative and improved plant varieties. Typically, the CRISPR-Cas9 gene-editing construct is delivered into target organisms via Agrobacterium tumefaciens-mediated transformation or biolistic methods. However, the incorporation of the CRISPR-Cas9 machinery increases the risk of off-target effects, causing unintended genomic alterations. Additionally, the introduction of exogenous DNA sequences, such as antibiotic resistance marker, raises public concerns regarding the biosafety and regulatory oversight of genetically modified organisms (GMOs), potentially hindering regulatory approval and commercialization. Here, we have engineered an integrated system comprising RUBY, LoxP::FRT/FLP and CRISPR/Cas9-sgRNA cassettes within a single construct, allowing visible color monitoring throughout process including genetic transform, positive transgenic and edited events screening, as well as exogenous DNA excision events, we refer to it as 'a visual monitoring DNA-free multi-gene editing system (VMDFGE)'. This system was introduced into poplar through Agrobacterium tumefaciens-mediated transformation, yielding transgenic poplars with a 75.0% visual screening rate, a 45.8% targeted mutation rate and a 54.5% excision rate for the entire integration system. This approach eliminates the concerns associated with off-target effects and GMO regulatory challenges. It offers significant potential for improvement of poplar, other woody plants and crop species while removing the foreign DNA.
CRISPR-Cas9系统已成为一种强大的分子手术刀,用于精确的基因组编辑,并深刻地革新了植物遗传学和育种,推动了创新和改良植物品种的开发。通常,CRISPR-Cas9基因编辑构建体通过根癌农杆菌介导的转化或生物弹道方法导入目标生物。然而,CRISPR-Cas9机制的整合增加了脱靶效应的风险,导致意外的基因组改变。此外,抗生素抗性标记等外源DNA序列的引入引发了公众对转基因生物生物安全性和监管监督的担忧,可能会阻碍监管批准和商业化。在此,我们设计了一个集成系统,在单个构建体中包含红宝石蛋白、LoxP::FRT/FLP和CRISPR/Cas9-sgRNA盒,允许在整个过程中进行可见颜色监测,包括基因转化、阳性转基因和编辑事件筛选,以及外源DNA切除事件,我们将其称为“视觉监测无DNA多基因编辑系统(VMDFGE)”。该系统通过根癌农杆菌介导的转化引入杨树,产生的转基因杨树的整个整合系统的视觉筛选率为75.0%,靶向突变率为45.8%,切除率为54.5%。这种方法消除了与脱靶效应和转基因生物监管挑战相关的担忧。它在去除外源DNA的同时,为杨树、其他木本植物和作物品种的改良提供了巨大潜力。