Reference genome-assisted identification of stem rust resistance gene Sr62 encoding a tandem kinase

The wild relatives and progenitors of wheat have been widely used as sources of disease resistance (R) genes. Molecular identification and characterization of these R genes facilitates their manipulation and tracking in breeding programmes. We developed a reference-quality genome assembly of the wild diploid wheat relative Aegilops sharonensis and used positional mapping, mutagenesis, RNA-Seq and transgenesis to identify the stem rust resistance gene Sr62, which was also transferred to common wheat. This gene encodes a tandem kinase, homologues of which exist across multiple taxa in the plant kingdom. Stable Sr62 transgenic wheat lines showed high levels of resistance against diverse isolates of the stem rust pathogen, highlighting the utility of Sr62 for deployment as part of a polygenic stack to maximize the durability of stem rust resistance.

Molecular analyses in wheat and Aegilops tauschii reveals a new orthologue of the leaf rust resistance gene Lr19 on 7DL chromosome of Ae. tauschii

Leaf rust is one of the most devastating wheat diseases worldwide, to which many resistance genes have been ‎successfully introgressed ‎from wheat wild relatives. Though the Thinopyrum ‎ponticum-derived leaf rust resistance gene Lr19, is widely effective worldwide and previous studies ‎have shown its likely presence in Aegilops tauschii, no ‎thorough investigation has been conducted to confirm this. The present study aimed to ‎examine the presence of Lr19 in Ae. tauschii using a collection of molecular and bioinformatic analysis. Accordingly, the Thatcher line was used as susceptible, and a Thatcher+Lr19 (TcLr19) and Agatha were used as resistant lines. CDHLQ pathotyping coupled with DNA markers genotyping verified the presence of an Lr19 orthologue on Ae. tauschii 7DL (AtLr19). Sequencing of the GB marker products from Ae. tauschii and TcLr19 showed 99% homology in these fragments, confirming phenotyping and genotyping results. Both isolated segments were matched to a putative melatonin biosynthesis gene, namely O-methyltransferase-2 (OMT2) mapped to 7DL, with 100% identity. A hierarchical gene network was reconstructed using all identified putative genes within a genomic region containing 2.5 cM upstream and downstream of the OMT2 gene. Results indicated that several numbers of important biotic stress-responsive genes such as RPM1, RGA2, TRIUR3, BURP12, and myosin-11, were located downstream of melatonin as a master regulator molecule through the OMT2 node. To our knowledge, this is the first report of finding an orthologue for ‎Lr19 in Ae. tauschii, which provides insights into the possible regulatory route of LR19.

Stripe rust resistance gene Yr34 (synonym Yr48) is located within a distal translocation of Triticum monococcum chromosome 5AmL into common wheat

Key messageThe stripe rust resistance geneYr34 was transferred to polyploid wheat chromosome 5AL from T. monococcumand has been used for over two centuries.Wheat stripe (or yellow) rust, caused by Puccinia striiformis f. sp. tritici (Pst), is currently among the most damaging fungal diseases of wheat worldwide. In this study, we report that the stripe rust resistance gene Yr34 (synonym Yr48) is located within a distal segment of the cultivated Triticum monococcum subsp. monococcum chromosome 5AmL translocated to chromosome 5AL in polyploid wheat. The diploid wheat species Triticum monococcum (genome AmAm) is closely related to T. urartu (donor of the A genome to polyploid wheat) and has good levels of resistance against the stripe rust pathogen. When present in hexaploid wheat, the T. monococcum Yr34 resistance gene confers a moderate level of resistance against virulent Pst races present in California and the virulent Chinese race CYR34. In a survey of 1,442 common wheat genotypes, we identified 5AmL translocations of fourteen different lengths in 17.5% of the accessions, with higher frequencies in Europe than in other continents. The old European wheat variety “Mediterranean” was identified as a putative source of this translocation, suggesting that Yr34 has been used for over 200 years. Finally, we designed diagnostic CAPS and sequenced-based markers that will be useful to accelerate the deployment of Yr34 in wheat breeding programs to improve resistance to this devastating pathogen.