Genetic dissection of powdery mildew resistance in emmer wheat WL509 via bulked segregated RNA sequencing.

Abstract

Emmer wheat (Triticum dicoccum, 2n = 4x = 28, AABB), as the ancestral species of common wheat, is a crucial gene donor for improving common wheat against powdery mildew, a destructive wheat disease worldwide. Cultivated emmer wheat accession WL509 exhibits broad and high level of resistance to powdery mildew. Using inheritance analysis, bulked segregated RNA sequencing (BSR-Seq) and molecular markers detection, we identified a dominant gene, tentatively designated PmWL509, and mapped it to 757.2-776.4 Mb interval on chromosome arm 2AL based on the reference genome of wild emmer (v2.0). PmWL509 was then mapped to the Pm4 locus using linked and diagnostic markers of Pm4. Homologous cloning and sequence alignment revealed that PmWL509 shares identical amino acid sequences with Pm4a but exhibits distinct resistance spectra and expression patterns. To explore potential regulatory mechanisms and key genes controlling resistance, 1,024 DEGs between resistant and susceptible bulks were annotated and analyzed by Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment. Six DEGs in the mapping interval and three pathogenesis-related (PR) genes were screened and evaluated by qRT-PCR when invaded by the Blumeria graminis f. sp. tritici (Bgt) isolate E09, and the result indicated that two DEGs TRIDC2AG078910 and TRIDC2AG081650 and two PR genes PR5 and PR9 could be considered to play a key role in the resistant pathway of PmWL509. The diagnostic marker JS717/JS718 was confirmed to be available for efficiently transferring PmWL509 into different wheat backgrounds.