Transgenic Brassica rapa plants over-expressing eIF(iso)4E variants show broad-spectrum Turnip mosaic virus (TuMV) resistance

Abstract

The protein-protein interaction between VPg (viral protein genome-linked) of potyviruses and eIF4E (eukaryotic initiation factor 4E) or eIF(iso)4E of their host plants is a critical step in determining viral virulence. In this study, we evaluated the approach of engineering broad-spectrum resistance in Chinese cabbage (Brassica rapa) to Turnip mosaic virus (TuMV), which is one of the most important potyviruses, by a systematic knowledge-based approach to interrupt the interaction between TuMV VPg and B. rapa eIF(iso) 4E. The seven amino acids in the cap-binding pocket of eIF(iso) 4E were selected on the basis of other previous results and comparison of protein models of cap-binding pockets, and mutated. Yeast two-hybrid assay and co-immunoprecipitation analysis demonstrated that W95L, K150L and W95L/K150E amino acid mutations of B. rapa eIF(iso) 4E interrupted its interaction with TuMV VPg. All eIF(iso) 4E mutants were able to complement an eIF4E-knockout yeast strain, indicating that the mutated eIF(iso) 4E proteins retained their function as a translational initiation factor. To determine whether these mutations could confer resistance, eIF(iso) 4E W95L, W95L/K150E and eIF(iso) 4E wild-type were over-expressed in a susceptible Chinese cabbage cultivar. Evaluation of the TuMV resistance of T-1 and T-2 transformants demonstrated that the over-expression of the eIF(iso) 4E mutant forms can confer resistance to multiple TuMV strains. These data demonstrate the utility of knowledge-based approaches for the engineering of broad-spectrum resistance in Chinese cabbage.