光形态发生
拟南芥
光敏色素
生物
磷酸酶
拟南芥
光敏色素A
脱磷
细胞生物学
磷酸化
突变体
蛋白磷酸酶2
转录因子
生物化学
基因
植物
红灯
作者
Xingbo Cai,Sang‐Hwa Lee,A. P. Jaime,Wenqiang Tang,Yu Sun,Enamul Huq
标识
DOI:10.1093/plcell/koae200
摘要
Abstract The phytochrome (phy) family of sensory photoreceptors modulates developmental programs in response to ambient light. Phys also control gene expression in part by directly interacting with the bHLH class of transcription factors, PHYTOCHROME-INTERACTING FACTORS (PIFs), and inducing their rapid phosphorylation and degradation. Several kinases have been shown to phosphorylate PIFs and promote their degradation. However, the phosphatases that dephosphorylate PIFs are less understood. Here, we describe four regulatory subunits of the Arabidopsis (Arabidopsis thaliana) protein PHOSPHATASE 2A (PP2A) family (B'α, B'β, B''α and B''β) that interact with PIF3 in yeast two-hybrid, in vitro and in vivo assays. The pp2ab''αβ and b''αβ/b'αβ mutants displayed short hypocotyls, while the overexpression of the B subunits induced longer hypocotyls compared to the wild type under red light. The light-induced degradation of PIF3 was faster in the b''αβ/b'αβ quadruple mutant compared to in the wild type. Consistently, immunoprecipitated PP2A A and B subunits directly dephosphorylated PIF3-MYC in vitro. RNA-seq analyses showed that B''α and B''β alter global gene expression in response to red light. PIFs (PIF1, PIF3, PIF4 and PIF5) are epistatic to these B subunits in regulating hypocotyl elongation under red light. Collectively, these data show an essential function of PP2A in dephosphorylating PIF3 to modulate photomorphogenesis in Arabidopsis.
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