Hassani-Mehraban Afshin, Brenkman A B, van den Broek N J F, Goldbach Rob, Kormelink Richard
Laboratory of Virology, Wageningen University, Binnenhaven 11, 6709 PD, Wageningen, The Netherlands.
Mol Plant Microbe Interact. 2009 Oct;22(10):1250-7. doi: 10.1094/MPMI-22-10-1250.
Extension of an inverted repeat transgene cassette, containing partial nucleoprotein (N) gene sequences from four different tomato-infecting Tospovirus spp. with a partial N gene sequence from the tomato strain of Tomato yellow ring virus (TYRV-t), renders transgenic Nicotiana benthamiana plants additionally resistant to this strain but not to the soybean strain of this Tospovirus sp. (TYRV-s), both strains exhibiting 14.4% nucleotide sequence divergence in their N genes. Surprisingly, coinoculation of the TYRV-t-resistant transgenic lines with both TYRV-t and TYRV-s resulted in rescue of the former. Mass-spectrometric analysis of the viral ribonucleocapsids accumulating in the transgenic plants showed the presence of the N proteins of both strains excluding hetero-encapsidation as rescue mechanism and indicating suppression of TYRV-t N gene transcript breakdown by RNA interference. Prior (Potato virus X [PVX]-vector-mediated) expression of the TYRV-s silencing suppressor (NS(s)) gene also allowed TYRV-t to break the resistance. This phenomenon was also observed when the homologous (TYRV-t) NS(s) gene was provided from a PVX replicon, demonstrating that TYRV can break RNA-mediated host resistance upon a priori expression of its NS(s) protein. Remarkably, mixed inoculation of TYRV-t with other Tospovirus spp. or nonrelated viruses did not result in resistance breaking, indicating that the rescuing activity of NS(s)-though based on suppressing RNA silencing-is species-dependent.
一个反向重复转基因盒的扩展,该转基因盒包含来自四种不同感染番茄的番茄斑萎病毒属病毒的部分核蛋白(N)基因序列以及番茄黄环病毒番茄株系(TYRV-t)的部分N基因序列,使得转基因本氏烟草植株对该株系具有额外抗性,但对该番茄斑萎病毒属病毒的大豆株系(TYRV-s)没有抗性,这两个株系在其N基因中表现出14.4%的核苷酸序列差异。令人惊讶的是,将TYRV-t抗性转基因株系与TYRV-t和TYRV-s同时接种,导致前者的抗性被解除。对转基因植物中积累的病毒核糖核蛋白进行质谱分析表明,两种株系的N蛋白都存在,排除了异源包装作为抗性解除机制,并表明RNA干扰抑制了TYRV-t N基因转录本的降解。预先(通过马铃薯X病毒[PVX]载体介导)表达TYRV-s沉默抑制子(NS(s))基因也使TYRV-t能够打破抗性。当从PVX复制子提供同源(TYRV-t)NS(s)基因时也观察到了这种现象,这表明TYRV在其NS(s)蛋白预先表达后能够打破RNA介导的宿主抗性。值得注意的是,将TYRV-t与其他番茄斑萎病毒属病毒或非相关病毒混合接种不会导致抗性打破,这表明NS(s)的拯救活性——尽管基于抑制RNA沉默——是物种依赖性的。