We expect to pin down the Rag5R gene and, time permitting, produce seeds of Rag5-expressing transgenic soybean in a high yielding variety that is originally aphid-susceptible.
Using VIGS constructs based on BPMV, ALSV, and CPSMV, we expect to complete the evaluation of the 16 Rps8 candidate genes using VIGS, and to determine the resistance potential of these genes. Completion of this objective will lay the foundation for further characterization of additional R loci.
We expect this series of QRL interrogation to extend the usefulness of VIGS to the analysis of genes in QRLs, allowing us to not only identify genes responsible for QRL traits, but also investigate their mode of functions.
The virus-mediated a vr expression procedure will be successfully established and optimized, providing breeders with a faster and more reliable assay for selecting R gene-containing progeny of crosses