| Literature DB >> 32583535 |
Miaomiao Li1, Lingli Dong1, Beibei Li1,2, Zhengzhong Wang3, Jingzhong Xie1, Dan Qiu4, Yahui Li4, Wenqi Shi5, Lijun Yang5, Qiuhong Wu1, Yongxing Chen1,2, Ping Lu1, Guanghao Guo1,2, Huaizhi Zhang1,2, Panpan Zhang1,2, Keyu Zhu1,2, Yiwen Li1, Yan Zhang3, Rongge Wang6, Chengguo Yuan6, Wei Liu7, Dazhao Yu5, Ming-Cheng Luo8, Tzion Fahima9, Eviatar Nevo9, Hongjie Li4, Zhiyong Liu1,2.
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.Entities:
Keywords: zzm321990Pm41zzm321990; Blumeria graminis f. sp. tritici; Triticum turgidum ssp. dicoccoides; coiled-coil-nucleotide-binding site-leucine-rich repeat (CC-NBS-LRR); positional cloning
Mesh:
Year: 2020 PMID: 32583535 DOI: 10.1111/nph.16761
Source DB: PubMed Journal: New Phytol ISSN: 0028-646X Impact factor: 10.151