Introgression of the highly effective Brassica rapa blackleg resistance gene Rlm11 into spring-type Brassica napus

Key Result

Genetic mapping of the blackleg resistance gene Rlm11 has been completed, Rlm11 has been incorporated into a spring-type B. napus lines. Molecular markers linked to Rlm11 were also generated, which will be shared with the industry and canola breeders to help improve blackleg control options for canola farmers.

Project Summary

Overview

Genetic resistance is a cost-effective, efficient and environmentally safe approach for protecting crops such as canola against various pathogens, including the blackleg-causing fungus, L. maculans, that does not respond to late-applied foliar fungicides. At the time of this project, 19 resistance (R) genes in Brassica have been identified (named as Rlm or LepR) that confer resistance to various isolates of L. maculans with matching Avirulence (Avr) genes.

However, tight rotations and new virulent isolates of L. maculans have likely led to resistance breakdown, creating a need for new sources of R genes. Field surveys across western Canadian canola farms found that blackleg races with the avirulence (Avr) gene AvrLm11 were highly prevalent at greater than 95 percent of fields across the Prairies. This makes the matching R gene, Rlm11, a highly relevant and effective gene used in canola cultivars in western Canada. Rlm11 was identified in a Brassica rapa accession; however, the genome location of the gene and associated markers were unknown, and incorporation of Rlm11 from B. rapa is challenging and time-consuming for canola breeders.

This four-year project aimed to address these issues by completing the genetic mapping of the blackleg resistance gene Rlm11, incorporating Rlm11 from the winter-type B. rapa to a spring-type B. napus, and generating molecular markers linked to Rlm11.

Methods and results

Researchers identified a B. rapa line that contained the race-specific resistance gene Rlm11. This homozygous Rlm11 line named ‘BR-11’ was then used to generate inter-species (B. napus x B. rapa) mapping populations by crossing BR-11 to the double haploid, blackleg susceptible B. napus line Topas DH16516. DNA from 96 F2 lines was applied to the Brassica 60K Illumina single nucleotide polymorphism (SNP) genotyping marker array and a genome scale SNP map was generated. Rlm11 was found to be positioned on the lower arm of chromosome A07 in a region between the previously mapped Rlm1 and the Rlm3-4-7-9 gene cluster.

To generate the spring type B. napus Rlm11 introgression lines, the B. napus susceptible line Topas DH16516 was chosen as the recipient parent. Several resistant individuals were selected for successive backcrossing to the susceptible Topas DH16516 parental line. Plants with a normal spring-type growth habit and good seed set were selected at each back-cross generation. Researchers advanced the generation of Topas-Rlm11 introgression lines through further back-crossing to produce and phenotype advanced back-cross populations. These advanced populations were screened using the KASP markers to generate and identify further recombination in the Rlm11 region. In the fall of 2021, advanced generations of Topas-Rlm11 introgression lines were harvested. These lines can be used to produce bulk seeds for distribution among canola breeders and agronomists in the near future.

Conclusions and advances

As a result of the project:

  • Researchers have completed the genetic mapping of the blackleg resistance gene Rlm11 and successfully developed Topas-Rlm11 introgression lines.
  • Researchers also generated molecular markers linked to Rlm11, which will be shared with the industry and canola breeders.
    • Rlm11 markers and Topas-Rlm11 introgression lines will allow canola breeders to offer a new and effective resistance gene to farmers.
    • Canola cultivars with Rlm11 combined with the blackleg race determination markers developed in this project will enable canola farmers to continue to effectively control the blackleg disease in the future when new varieties incorporate Rlm11 resistance.