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A CaCDPK29-CaWRKY27b module promotes CaWRKY40-mediated thermotolerance and immunity to Ralstonia solanacearum in pepper

文献类型: 外文期刊

作者: Yang, Sheng 1 ; Cai, Weiwei 1 ; Shen, Lei 1 ; Cao, Jianshen 1 ; Liu, Cailing 4 ; Hu, Jiong 1 ; Guan, Deyi 1 ; He, Shuilin 1 ;

作者机构: 1.Fujian Agr & Forestry Univ, Natl Educ Minist, Key Lab Plant Genet Improvement & Comprehens Util, Fuzhou 350002, Fujian, Peoples R China

2.Fujian Agr & Forestry Univ, Key Lab Appl Genet Univ Fujian Prov, Fuzhou 350002, Fujian, Peoples R China

3.Fujian Agr & Forestry Univ, Agr Coll, Fuzhou 350002, Fujian, Peoples R China

4.Fujian Acad Agr Sci, Inst Soil & Fertilizer, Fuzhou 350002, Fujian, Peoples R China

关键词: CDPK; high temperature high humidity; immunity; pepper (Capsicum annuum); Ralstonia solanacearum; WRKY

期刊名称:NEW PHYTOLOGIST ( 影响因子:10.323; 五年影响因子:10.768 )

ISSN: 0028-646X

年卷期: 2022 年 233 卷 4 期

页码:

收录情况: SCI

摘要: CaWRKY40 in pepper (Capsicum annuum) promotes immune responses to Ralstonia solanacearum infection (RSI) and to high-temperature, high-humidity (HTHH) stress, but how it interacts with upstream signalling components remains poorly understood. Here, using approaches of reverse genetics, biochemical and molecular biology we functionally characterised the relationships among the WRKYGMK-containing WRKY protein CaWRKY27b, the calcium-dependent protein kinase CaCDPK29, and CaWRKY40 during pepper response to RSI or HTHH. Our data indicate that CaWRKY27b is upregulated and translocated from the cytoplasm to the nucleus upon phosphorylation of Ser137 in the nuclear localisation signal by CaCDPK29. Using electrophoretic mobility shift assays and microscale thermophoresis, we observed that, due to the replacement of Q by M in the conserved WRKYGQK, CaWRKY27b in the nucleus failed to bind to W-boxes in the promoters of immunity- and thermotolerance-related marker genes. Instead, CaWRKY27b interacted with CaWRKY40 and promoted its binding and positive regulation of the tested marker genes including CaNPR1, CaDEF1 and CaHSP24. Notably, mutation of the WRKYGMK motif in CaWRKY27b to WRKYGQK restored the W-box binding ability. Our data therefore suggest that CaWRKY27b is phosphorylated by CaCDPK29 and acts as a transcriptional activator of CaWRKY40 during the pepper response to RSI and HTHH.

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