Reduction of OsMPK6 activity by a R89K mutation induces cell death and bacterial blight resistance in rice

文献类型： 外文期刊

第一作者： Wang, Dongfei

作者： Wang, Dongfei;Wang, Hong;Liu, Qunen;Tu, Ranran;Zhou, Xingpeng;Zhang, Yingxin;Wu, Weixun;Yu, Ping;Chen, Daibo;Zhan, Xiaodeng;Cao, Liyong;Cheng, Shihua;Shen, Xihong;Wang, Dongfei;Wang, Hong;Liu, Qunen;Tu, Ranran;Zhou, Xingpeng;Zhang, Yingxin;Wu, Weixun;Yu, Ping;Chen, Daibo;Zhan, Xiaodeng;Cao, Liyong;Cheng, Shihua;Shen, Xihong

作者机构：

关键词： Rice (Oryza sativa L; ); Lesion mimic mutant; Cell death; Defense response; OsMPK6

期刊名称：PLANT CELL REPORTS （ 影响因子：3.825； 五年影响因子：3.686 ）

ISSN： 0721-7714

年卷期： 2021 年 40 卷 5 期

页码：

收录情况： SCI

摘要： Key message The R89 is essential for the kinase activity of OsMPK6 which negatively regulates cell death and defense response in rice. Mitogen-activated protein kinase cascade plays critical roles in various vital activities, including the plant immune response, but the mechanisms remain elusive. Here, we identified and characterized a rice lesion mimic mutant osmpk6 which displayed hypersensitive response-like lesions in company with cell death and hydrogen peroxide hyperaccumulation. Map-based cloning and complementation demonstrated that a G702A single-base substitution in the second exon of OsMPK6 led to the lesion mimic phenotype of the osmpk6 mutant. OsMPK6 encodes a cytoplasm and nucleus-targeted mitogen-activated protein kinase and is expressed in the various organs. Compared with wild type, the osmpk6 mutant exhibited high resistance to the bacterial pathogen Xanthomonas oryzae pv. oryzae (Xoo), likely due to the increased ROS production induced by flg22 and chitin and up-regulated expression of genes involved in pathogenesis, as well as activation of SA and JA signaling pathways after inoculation. By contrast, the OsMPK6-overexpression line (OE-1) was found to be susceptible to the bacterial pathogens, indicating that OsMPK6 negatively regulated Xoo resistance. Furthermore, the G702A single-base substitution caused a R89K mutation at both polypeptide substrate-binding site and active site of OsMPK6, and kinase activity assay revealed that the R89K mutation led to reduction of OsMPK6 activity, suggesting that the R89 is essential for the function of OsMPK6. Our findings provide insight into a vital role of the R89 of OsMPK6 in regulating cell death and defense response in rice.

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