Poster
Abdulrahman Alhabsi
Postdoctoral Researcher
King Abdullah University of Science and Technology
Thuwal, Makkah, Saudi Arabia
Danni Zou
King Abdullah University of Science and Technology
Thuwal, Makkah, Saudi Arabia
Francisco Ayala
PhD Student
King Abdullah University of Science and Technology
Jeddah, Makkah, Saudi Arabia
Radim Svačina
King Abdullah University of Science and Technology
Thuwal, Makkah, Saudi Arabia
Jing Lu
King Abdullah University of Science and Technology
Thuwal, Makkah, Saudi Arabia
Renad Al Ahmadi
King Abdullah University of Science and Technology
Thuwal, Makkah, Saudi Arabia
Samiya Masood
King Abdullah University of Science and Technology
Thuwal, Makkah, Saudi Arabia
Serine Duhaithem
King Abdullah University of Science and Technology
Thuwal, Makkah, Saudi Arabia
Yagiz Alagoz
Post-doctoral Fellow
King Abdullah University of Science and Technology
Jeddah, Makkah, Saudi Arabia
Brande Wulff
Prof. Dr.
King Abdullah University of Science and Technology (KAUST)
Thuwal, Makkah, Saudi Arabia
Global wheat production is constrained by pests and diseases, historically causing devastating epidemics and famines. Conventional and transgene stacking of resistance (R) genes can provide broad-spectrum resistance in wheat. However, selecting effective wheat R genes for stacking remains a challenge. While >100 R genes have been cloned from wheat and its wild relatives, many have either partial or undocumented efficacy. Background resistance often limits the scope of pathogen isolates that can be tested for variation in virulence against a particular R gene. Therefore, we aim to assess the efficacy of ‘all’ cloned wheat rust R genes, based on gene synthesis and transformation into universally susceptible genotypes to create the Wheat Rust Resistance Gene Library. We have selected susceptible check lines used by breeders for comprehensive stem, stripe, and leaf rust pathogenecity tests and transformation competence. We will transform the selected lines with individual cloned R genes, to create an isogenic library. With international collaborators we will evaluate the efficacy of the cloned R genes by deep phenotyping. Additionally, we are testing the function of shortened R genes (where the non-coding regions have been pruned), as a strategy to mitigate the size limitation for R gene stacking. Identifying R genes with the highest efficacy will facilitate the judicious design and construction of R gene stacks that confer durable and broad-spectrum rust resistance.