Poster
Zhu Fang
Institute Of Plant Protection, Chinese Academy Of Agricultural Sciences
Beijing, Beijing, China (People's Republic)
Xinru Zhao
Institute of Plant Protection, Chinese Academy of Agricultural Sciences
Beijing, Beijing, China (People's Republic)
Min Du
Institute of Plant Protection, Chinese Academy of Agricultural Sciences
Beijing, Beijing, China (People's Republic)
Xinyi Xu
Institute of Plant Protection, Chinese Academy of Agricultural Sciences
Beijing, Beijing, China (People's Republic)
Hui Zhou
Institute of Plant Protection, Chinese Academy of Agricultural Sciences
Beijing, Beijing, China (People's Republic)
Wei Guo
Institute of Food Science and Technology, Chinese Academy of Agricultural Sciences
Beijing, Beijing, China (People's Republic)
Xueping Zhou
Institute of Plant Protection, Chinese Academy of Agricultural Sciences
Beijing, Beijing, China (People's Republic)
Xiuling Yang (she/her/hers)
Institute of Plant Protection, Chinese Academy of Agricultural Sciences
Beijing, Beijing, China
Plant viruses have been modified as important tools to express heterologous proteins in plants, yet the yield of target proteins is often limited by plant antiviral defenses. In this study, we found that the mRNA level of a glycine-rich cell wall structural protein (NbGRP) was significantly upregulated in response to tomato brown rugose fruit virus (ToBRFV) infection. We show that NbGRP is an antiviral host factor by gain and loss-of function assays. We demonstrated that CRISPR/Cas9-based genome editing of NbGRP not only promotes plant growth but also significantly enhances the production of heterologous proteins mediated by three different plant viral vectors. Our study provides a promising strategy to optimize plant viral vector-based biofactories, with potential applications in biotechnology.