A CNL protein in wild emmer wheat confers powdery mildew resistance

Miaomiao Li(Chinese Academy of Sciences), Lingli Dong(Chinese Academy of Sciences), Beibei Li(Chinese Academy of Sciences), Zhengzhong Wang(China Agricultural University), Jingzhong Xie(Chinese Academy of Sciences), Dan Qiu(Chinese Academy of Agricultural Sciences), Yahui Li(Chinese Academy of Sciences), Wenqi Shi(Institute of Plant Protection), Lijun Yang(Institute of Plant Protection), Qiuhong Wu(Chinese Academy of Sciences), Yongxing Chen(Chinese Academy of Sciences), Ping Lu(Chinese Academy of Sciences), Guanghao Guo(Chinese Academy of Sciences), Huaizhi Zhang(Chinese Academy of Sciences), Panpan Zhang(Chinese Academy of Sciences), Keyu Zhu(Chinese Academy of Sciences), Yiwen Li(Chinese Academy of Sciences), Yan Zhang(China Agricultural University), Rongge Wang(Hebei University of Technology), Chengguo Yuan(Hebei University of Technology), Wei Liu(Beijing VDJBio (China)), Dazhao Yu(Institute of Plant Protection), Ming‐Cheng Luo(University of California, Davis), Tzion Fahima(Carmel (Israel)), Eviatar Nevo(Carmel (Israel)), Hongjie Li(Chinese Academy of Agricultural Sciences), Zhiyong Liu(Chinese Academy of Sciences)
New Phytologist
June 25, 2020
Cited by 162

Abstract

Powdery mildew, a fungal disease caused by Blumeria graminis f. sp. tritici (Bgt), has a serious impact on wheat production. Loss of resistance in cultivars prompts a continuing search for new sources of resistance. Wild emmer wheat (Triticum turgidum ssp. dicoccoides, WEW), the progenitor of both modern tetraploid and hexaploid wheats, harbors many powdery mildew resistance genes. We report here the positional cloning and functional characterization of Pm41, a powdery mildew resistance gene derived from WEW, which encodes a coiled-coil, nucleotide-binding site and leucine-rich repeat protein (CNL). Mutagenesis and stable genetic transformation confirmed the function of Pm41 against Bgt infection in wheat. We demonstrated that Pm41 was present at a very low frequency (1.81%) only in southern WEW populations. It was absent in other WEW populations, domesticated emmer, durum, and common wheat, suggesting that the ancestral Pm41 was restricted to its place of origin and was not incorporated into domesticated wheat. Our findings emphasize the importance of conservation and exploitation of the primary WEW gene pool, as a valuable resource for discovery of resistance genes for improvement of modern wheat cultivars.


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