拟南芥
磷酸化
生物
相扑蛋白
细胞生物学
转录因子
磷酸化级联
激酶
遗传学
蛋白质磷酸化
蛋白激酶A
泛素
基因
突变体
作者
Fanglin Zhou,Somesh Singh,Jie Zhang,Fang Qiu,Chongyang Li,Jiawen Wang,Chunzhao Zhao,Pengcheng Wang,Chao‐Feng Huang
标识
DOI:10.1016/j.molp.2022.11.010
摘要
Aluminum (Al) toxicity can seriously restrict crop production on acidic soils, which comprise 40% of the world's potentially arable land. The zinc finger transcription factor STOP1 has a conserved and essential function in mediating plant Al resistance. Al stress induces STOP1 accumulation via post-transcriptional regulatory mechanisms. However, the upstream signaling pathway involved in Al-triggered STOP1 accumulation remains unclear. Here, we report that the MEKK1-MKK1/2-MPK4 cascade positively regulates STOP1 phosphorylation and stability. Mutations of MEKK1, MKK1/2, or MPK4 lead to decreased STOP1 stability and Al resistance. Al stress induces the kinase activity of MPK4, which interacts with and phosphorylates STOP1. The phosphorylation of STOP1 reduces its interaction with the F-box protein RAE1 that mediates STOP1 degradation, thereby leading to enhanced STOP1 stability and Al resistance. Taken together, our results suggest that the MEKK1-MKK1/2-MPK4 cascade is important for Al signaling and confers Al resistance through phosphorylation-mediated enhancement of STOP1 accumulation in Arabidopsis.
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