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D6 protein kinase in root xylem benefiting resistance to Fusarium reveals infection and defense mechanisms in tung trees  ( SCI-EXPANDED收录)   被引量:2

文献类型:期刊文献

英文题名:D6 protein kinase in root xylem benefiting resistance to Fusarium reveals infection and defense mechanisms in tung trees

作者:Zhang, Qiyan[1,2] Wu, Liwen[1,2] Yin, Hengfu[1,2] Xu, Zilong[1,2] Zhao, Yunxiao[1,2] Gao, Ming[1,2] Wu, Hong[2] Chen, Yicun[1,2] Wang, Yangdong[1,2]

第一作者:Zhang, Qiyan

通信作者:Chen, YC[1];Wang, YD[1];Chen, YC[2];Wang, YD[2]

机构:[1]Chinese Acad Forestry, State Key Lab Free Genet & Breeding, Beijing 100091, Peoples R China;[2]Chinese Acad Forestry, Res Inst Subtrop Forestry, Hangzhou 311400, Zhejiang, Peoples R China

年份:2021

卷号:8

期号:1

外文期刊名:HORTICULTURE RESEARCH

收录:;WOS:【SCI-EXPANDED(收录号:WOS:000713155100015)】;

基金:The work was financially supported by the National Natural Science Foundation of China (31971685) and the Fundamental Research Funds for the Central Nonprofit Research Institution of Chinese Academy of Forestry (CAFYBB2019ZB002).

语种:英文

摘要:Fusarium oxysporum, a global soil-borne pathogen, causes severe disease in various cultivated plants. The mechanism underlying infection and resistance remains largely elusive. Vernicia fordii, known as the tung tree, suffers from disease caused by F. oxysporum f. sp. fordiis (Fof-1), while its sister species V. montana displays high resistance to Fof-1. To investigate the process of infection and resistance ability, we demonstrated that Fof-1 can penetrate the epidermis of root hairs and then centripetally invade the cortex and phloem in both species. Furthermore, Fof-1 spread upwards through the root xylem in susceptible V. fordii trees, whereas it failed to infect the root xylem in resistant V. montana trees. We found that D6 PROTEIN KINASE LIKE 2 (VmD6PKL2) was specifically expressed in the lateral root xylem and was induced after Fof-1 infection in resistant trees. Transgenic analysis in Arabidopsis and tomato revealed that VmD6PKL2 significantly enhanced resistance in both species, whereas the d6pkl2 mutant displayed reduced resistance against Fof-1. Additionally, VmD6PKL2 was identified to interact directly with synaptotagmin (VmSYT3), which is specifically expressed in the root xylem and mediates the negative regulation responding to Fof-1. Our data suggested that VmD6PKL2 could act as a resistance gene against Fof-1 through suppression of VmSYT3-mediated negative regulation in the lateral root xylem of the resistant species. These findings provide novel insight into Fusarium wilt resistance in plants.

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