4.7 Article

Genetically Dissecting the Novel Powdery Mildew Resistance Gene in Wheat Breeding Line PBDH1607

Journal

PLANT DISEASE
Volume 106, Issue 8, Pages 2145-2154

Publisher

AMER PHYTOPATHOLOGICAL SOC
DOI: 10.1094/PDIS-12-21-2771-RE

Keywords

BSR-Seq; disease resistance; marker-assisted selection; wheat powdery mildew

Categories

Funding

  1. National Natural Science Foundation of China [32072053, 31971874, 32171990]
  2. Key Research and Development Program of Shandong Province [2020CXGC010805]
  3. Taishan Scholars Project [tsqn201812123]
  4. Open Project Funding of the State Key Laboratory of Crop Stress Adaptation and Improvement [CX1130A0920014]

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In this study, a new dominant gene PmPBDH was identified as the source of high resistance to powdery mildew in wheat breeding line PBDH1607. Genetic analysis and mapping revealed that PmPBDH is located on chromosome arm 4AL within a specific interval. Candidate genes associated with PmPBDH were also identified, and linked markers were developed for marker-assisted breeding.
Powdery mildew is one of the most destructive diseases in wheat production. Identifying novel resistance genes and deploying them in new cultivars is the most effective approach to minimize wheat losses caused by powdery mildew. In this study, wheat breeding line PBDH1607 showed high resistance to powdery mildew at both the seedling and adult plant stages. Genetic analysis of the seedling data demonstrated that the resistance was controlled by a single dominant gene, tentatively designated PmPBDH. The Delta SNP index based on bulked segregant RNA sequencing indicated that PmPBDH was associated with an interval of about 30.8 Mb (713.5 to 744.3 Mb) on chromosome arm 4AL. Using newly developed markers, we mapped PmPBDH to a 3.2-cM interval covering 7.1 Mb (719,055,516 to 726,215,121 bp). This interval differed from those of Pm61 (717,963,176 to 719,260,469 bp), MlIW30 (732,769,506 to 732,790,522 bp), and MlNSF10 (729,275,816 to 731,365,462 bp) reported on the same chromosome arm. PmPBDH also differed from Pm61, MlIW30, and MlNSF10 by its response spectrum, origin, or inheritance mode, suggesting that PmPBDH should be a new Pm gene. In the candidate interval, five genes were found to be associated with PmPBDH via time course gene expression analysis, and thus they are candidate genes of PmPBDH. Six closely linked markers, including two kompetitive allele-specific PCR markers, were confirmed to be applicable for tracking PmPBDH in marker-assisted breeding.

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