Luo Xiaoyan, Dou Ying, Lang Yuxuan, Zhao Huamei, Liu Xinling, Zhang Xiaoli, Li Yuxing, Liang Dong, Xia Hui
College of Horticulture, Sichuan Agricultural University, Huimin Road 211#, Chengdu, 611130, China.
BMC Plant Biol. 2025 Aug 9;25(1):1056. doi: 10.1186/s12870-025-07112-6.
CRISPR/Cas9 technology has garnered increasing attention for its simplicity and precision in genome editing, making it an indispensable tool for gene function research and crop genetic improvement. However, the inefficiency and time-consuming nature of genetic transformation continue to pose substantial challenges to its widespread application in woody plants.
In this study, we developed a rapid and efficient Agrobacterium-mediated transformation system using petioles as explants for kiwifruit. Positive resistant seedlings were obtained within three months by inoculating on MS medium supplemented with 2.0 mg·L 6-benzylaminopurine (6-BA), 0.2 mg·L naphthaleneacetic acid (NAA), and 10 mg·L hygromycin, which was faster than using leaves as explants. Using this system, CRISPR/Cas9-mediated editing of phytoene desaturase (AcPDS) and ζ-carotene desaturase (AcZDS) achieved an editing efficiency of 20%. Transgenic kiwifruit lines with edited AcZDS exhibited a significant reduction in carotenoid content.
Overall, we established an efficient Agrobacterium-mediated transformation system using petioles as explants, which is applicable for CRISPR/Cas9-mediated gene editing in kiwifruit, thereby facilitating functional gene studies and genetic improvement.
CRISPR/Cas9技术因其在基因组编辑中的简便性和精确性而受到越来越多的关注,使其成为基因功能研究和作物遗传改良不可或缺的工具。然而,遗传转化的低效性和耗时性继续对其在木本植物中的广泛应用构成重大挑战。
在本研究中,我们开发了一种快速高效的农杆菌介导的转化系统,该系统使用叶柄作为猕猴桃的外植体。通过接种在添加了2.0 mg·L 6-苄基腺嘌呤(6-BA)、0.2 mg·L萘乙酸(NAA)和10 mg·L潮霉素的MS培养基上,在三个月内获得了阳性抗性幼苗,这比使用叶片作为外植体更快。使用该系统,对八氢番茄红素去饱和酶(AcPDS)和ζ-胡萝卜素去饱和酶(AcZDS)进行CRISPR/Cas9介导的编辑,编辑效率达到20%。AcZDS编辑的转基因猕猴桃株系的类胡萝卜素含量显著降低。
总体而言,我们建立了一种以叶柄为外植体的高效农杆菌介导的转化系统,该系统适用于猕猴桃中CRISPR/Cas9介导的基因编辑,从而促进功能基因研究和遗传改良。