Huai Dongxin, Wu Jie, Xue Xiaomeng, Hu Meiling, Zhi Chenyang, Pandey Manish K, Liu Nian, Huang Li, Bai Dongmei, Yan Liying, Chen Yuning, Wang Xin, Kang Yanping, Wang Zhihui, Jiang Huifang, Lei Yong, Varshney Rajeev K, Liao Boshou
Key Laboratory of Biology and Genetic Improvement of Oil Crops, Ministry of Agriculture and Rural Affairs, Oil Crops Research Institute of Chinese Academy of Agricultural Sciences, Wuhan, China.
Center of Excellence in Genomics and Systems Biology (CEGSB), International Crops Research Institute of the Semi-Arid Tropics (ICRISAT), Hyderabad, India.
Front Plant Sci. 2023 Mar 1;14:1123644. doi: 10.3389/fpls.2023.1123644. eCollection 2023.
Peanut ( L.), one of the leading oilseed crops worldwide, is an important source of vegetable oil, protein, minerals and vitamins. Peanut is widely cultivated in Asia, Africa and America, and China is the largest producer and consumer of peanut. Genetic engineering has shown great potential to alter the DNA makeup of an organism which is largely hindered by the low transformation and screening efficiency including in peanut. DsRed2 is a reporter gene widely utilized in genetic transformation to facilitate the screening of transformants, but never used in peanut genetic transformation. In this study, we have demonstrated the potential of the red fluorescence protein DsRed2 as a visual reporter to improve screening efficiency in peanut. DsRed2 was firstly expressed in protoplasts isolated from peanut cultivar Zhonhua 12 by PEG, and red fluorescence was successfully detected. Then, DsRed2 was expressed in peanut plants Zhonghua 12 driven by 35S promoter -mediated transformation. Red fluorescence was visually observed in calli and regenerated shoots, as well as in roots, leaves, flowers, fresh pod shells and mature seeds, suggesting that transgenic screening could be initiated at the early stage of transformation, and continued to the progeny. Upon screening with DsRed2, the positive plant rate was increased from 56.9% to 100%. The transgenic line was then used as the male parent to be crossed with Zhonghua 24, and the hybrid seeds showed red fluorescence as well, indicating that DsRed2 could be applied to hybrid plant identification very efficiently. DsRed2 was also expressed in hairy roots of Huayu 23 -mediated transformation, and the transgenic roots were easily selected by red fluorescence. In summary, the DsRed2 is an ideal reporter to achieve maximum screening efficiency and accuracy in peanut genetic transformation.
花生(Arachis hypogaea L.)是全球主要的油料作物之一,是植物油、蛋白质、矿物质和维生素的重要来源。花生在亚洲、非洲和美洲广泛种植,中国是花生的最大生产国和消费国。基因工程在改变生物体的DNA组成方面显示出巨大潜力,但在包括花生在内的许多植物中,由于转化和筛选效率低,这一潜力受到很大阻碍。DsRed2是一种在遗传转化中广泛用于促进转化体筛选的报告基因,但从未用于花生遗传转化。在本研究中,我们证明了红色荧光蛋白DsRed2作为视觉报告基因在提高花生筛选效率方面的潜力。DsRed2首先通过聚乙二醇(PEG)在从花生品种中花12分离的原生质体中表达,并成功检测到红色荧光。然后,通过35S启动子介导的转化,将DsRed2在花生品种中花12植株中表达。在愈伤组织、再生芽以及根、叶、花、新鲜荚壳和成熟种子中都能直观地观察到红色荧光,这表明转基因筛选可以在转化的早期阶段开始,并持续到后代。用DsRed2进行筛选后,阳性植株率从56.9%提高到100%。然后将转基因株系用作父本与中花24杂交,杂交种子也显示出红色荧光,这表明DsRed2可以非常有效地应用于杂交植物鉴定。DsRed2还通过介导转化在花育23的毛状根中表达,转基因根很容易通过红色荧光筛选出来。总之,DsRed2是在花生遗传转化中实现最大筛选效率和准确性的理想报告基因。