Yin Jinlong, Liu Hui, Xiang Wenyang, Jin Tongtong, Guo Dongquan, Wang Liqun, Zhi Haijian
National Center for Soybean Improvement, National Key Laboratory for Crop Genetics and Germplasm Enhancement, Nanjing Agricultural University, Weigang 1, Nanjing, 210095, People's Republic of China.
Jilin Academy of Agricultural Sciences, Changchun, 130033, People's Republic of China.
AMB Express. 2019 Jul 24;9(1):116. doi: 10.1186/s13568-019-0840-3.
Infectious clone vectors used widely in genetic research. While constructing soybean mosaic virus (SMV) clone vectors, we found that transformed Agrobacterium grew significantly different depending on the viral strains used. In particular, the clone vectors constructed with SMV SC15 significantly suppressed the growth of Agrobacterium. Recombinant and truncated virus vector experiments showed that the polymorphism of a P1 protein coding sequence of SC15 leads to the growth inhibition of Agrobacterium. But the lack of other protein encoding sequences, except for the sequence encoding coat protein, should reduce the ability of SC15 to suppress Agrobacterium growth. A vector (pCB301-attL-SC15P) compatible with the Gateway cloning system was constructed using this Agrobacterium inhibitory sequence. The results from the LR recombination reaction with pCB301-attL-SC15P and Agrobacterium transformation showed the valuable application potential of the Agrobacterium inhibitory sequence to serve as a negative screening factor for effective recombinant clone screening in Agrobacterium.
感染性克隆载体在基因研究中广泛应用。在构建大豆花叶病毒(SMV)克隆载体时,我们发现转化的农杆菌生长情况因所用病毒株的不同而有显著差异。特别是,用SMV SC15构建的克隆载体显著抑制了农杆菌的生长。重组和截短病毒载体实验表明,SC15的P1蛋白编码序列的多态性导致了农杆菌的生长抑制。但除了编码外壳蛋白的序列外,其他蛋白质编码序列的缺失应该会降低SC15抑制农杆菌生长的能力。利用这种农杆菌抑制序列构建了与Gateway克隆系统兼容的载体(pCB301-attL-SC15P)。pCB301-attL-SC15P与农杆菌转化的LR重组反应结果表明,农杆菌抑制序列作为农杆菌中有效重组克隆筛选的阴性筛选因子具有重要的应用潜力。