脱落酸
发起人
磷酸化
转录因子
细胞生物学
化学
磷酸酶
激酶
信号转导
受体
基因
分子生物学
基因表达
生物
生物化学
作者
Xiaoji Wang,Can Guo,Jing Peng,Cong Li,Fangfang Wan,Shaoman Zhang,Yangyang Zhou,Yan Yan,Lijuan Qi,Kaiwen Sun,Shuhua Yang,Zhizhong Gong,Jigang Li
摘要
Summary Group A protein phosphatase 2Cs ( PP 2Cs) are abscisic acid ( ABA ) co‐receptors that negatively regulate the ABA signaling pathway by inhibiting the downstream Sn RK 2 protein kinases. It has long been observed that exogenous ABA treatments dramatically induce the expression of group A PP 2C genes, but the underlying molecular mechanisms and the biological significance remain largely unknown. Here, by using GUS reporter transgenic lines in which various lengths of ABI1 and ABI2 promoters were used to drive GUS gene expression, we defined the promoter fragments that confer ABA inducibility to ABI1 and ABI2 . We further showed that ABRE ‐binding factors ( ABF s), the bZIP family transcription factors, directly bind to the promoters of group A PP2C genes, and mediate rapid induction of their expression on exogenous ABA treatments. Moreover, our data indicated that ABA dramatically induces the expression of ABF genes and the accumulation of endogenous ABF proteins, and that ABF s themselves are involved in this induction, thus providing another layer of ABA regulation towards ABF proteins in addition to the well‐characterized ABA ‐induced phosphorylation by Sn RK 2 protein kinases. Together, our data demonstrate that ABF s mediate rapid ABA induction of group A PP2C genes, thus playing a role in the negative feedback regulation of ABA signaling.
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