A rare gain of function mutation in a wheat tandem kinase confers resistance to powdery mildew

Ping Lu(Chinese Academy of Sciences), Li Guo(China Agricultural University), Zhenzhong Wang(China Agricultural University), Beibei Li(Chinese Academy of Sciences), Jing Li(Beijing University of Agriculture), Yahui Li(Chinese Academy of Agricultural Sciences), Dan Qiu(Chinese Academy of Agricultural Sciences), Wenqi Shi(Institute of Plant Protection), Lijun Yang(Institute of Plant Protection), Ning Wang(Chinese Academy of Sciences), Guanghao Guo(Chinese Academy of Sciences), Jingzhong Xie(Chinese Academy of Sciences), Qiuhong Wu(Chinese Academy of Sciences), Yongxing Chen(Chinese Academy of Sciences), Miaomiao Li(Chinese Academy of Sciences), Huaizhi Zhang(Chinese Academy of Sciences), Lingli Dong(Chinese Academy of Sciences), Panpan Zhang(Chinese Academy of Sciences), Keyu Zhu(Chinese Academy of Sciences), Dazhao Yu(Institute of Plant Protection), Yan Zhang(China Agricultural University), Karin R. Deal(University of California, Davis), Naxin Huo(Western Regional Research Center), Cuimin Liu(Chinese Academy of Sciences), Ming‐Cheng Luo(University of California, Davis), Jan Dvořák(University of California, Davis), Yong Gu(Western Regional Research Center), Hongjie Li(Chinese Academy of Agricultural Sciences), Zhiyong Liu(Institute of Genetics and Developmental Biology)
Nature Communications
February 3, 2020
Cited by 253Open Access
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Abstract

Powdery mildew, caused by Blumeria graminis f. sp. tritici (Bgt), is one of the most destructive diseases that pose a great threat to wheat production. Wheat landraces represent a rich source of powdery mildew resistance. Here, we report the map-based cloning of powdery mildew resistance gene Pm24 from Chinese wheat landrace Hulutou. It encodes a tandem kinase protein (TKP) with putative kinase-pseudokinase domains, designated WHEAT TANDEM KINASE 3 (WTK3). The resistance function of Pm24 was validated by transgenic assay, independent mutants, and allelic association analyses. Haplotype analysis revealed that a rare 6-bp natural deletion of lysine-glycine codons, endemic to wheat landraces of Shaanxi Province, China, in the kinase I domain (Kin I) of WTK3 is critical for the resistance function. Transgenic assay of WTK3 chimeric variants revealed that only the specific two amino acid deletion, rather than any of the single or more amino acid deletions, in the Kin I of WTK3 is responsible for gaining the resistance function of WTK3 against the Bgt fungus.


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