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

Author:

Liang Xiao1,Xu Hongxing2,Zhu Shanying3,Zheng Yongshen4,Zhong Wen5,Li Haosheng4,Niu Liping6,Wu Liru1,Zhang Lipei1,Song Jiancheng1,He Huagang3,Liu Cheng4,Ma Pengtao1ORCID

Affiliation:

1. College of Life Sciences, Yantai University, Yantai, Shandong 264005, China

2. School of Life Sciences, Henan University, Kaifeng, Henan 475004, China

3. School of Life Sciences, Jiangsu University, Zhenjiang, Jiangsu 212013, China

4. Crop Research Institute, Shandong Academy of Agricultural Sciences, Jinan, Shandong 250100, China

5. Shandong Seed Administration Station, Jinan, Shandong 250100, China

6. State Key Laboratory of Hybrid Rice, College of Life Sciences, Wuhan University, Wuhan, Hubei 430072, China

Abstract

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 ΔSNP 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.

Funder

National Natural Science Foundation of China

Key Research and Development Program of Shandong Province

Taishan Scholars Project

Open Project Funding of the State Key Laboratory of Crop Stress Adaptation and Improvement

Publisher

Scientific Societies

Subject

Plant Science,Agronomy and Crop Science

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