Structural Plant Biology Laboratory, Department of Plant Sciences, University of Geneva, 30 Quai E. Ansermet, Geneva 1211, Switzerland.
Plant Cell Physiol. 2024 Nov 13;65(10):1674-1688. doi: 10.1093/pcp/pcae056.
Brassinosteroids (BRs) are vital plant steroid hormones sensed at the cell surface by a membrane signaling complex comprising the receptor kinase BRI1 and a SERK family co-receptor kinase. Activation of this complex lead to dissociation of the inhibitor protein BKI1 from the receptor and to differential phosphorylation of BZR1/BES1 transcription factors by the glycogen synthase kinase 3 protein BIN2. Many phosphoproteins of the BR signaling pathway, including BRI1, SERKs, BKI1 and BZR1/BES1 can associate with 14-3-3 proteins. In this study, we use quantitative ligand binding assays to define the minimal 14-3-3 binding sites in the N-terminal lobe of the BRI1 kinase domain, in BKI1, and in BZR1 from Arabidopsis thaliana. All three motifs require to be phosphorylated to specifically bind 14-3-3s with mid- to low-micromolar affinity. BR signaling components display minimal isoform preference within the 14-3-3 non-ε subgroup. 14-3-3λ and 14-3-3 ω isoform complex crystal structures reveal that BKI1 and BZR1 bind as canonical type II 14-3-3 linear motifs. Disruption of key amino acids in the phosphopeptide binding site through mutation impairs the interaction of 14-3-3λ with all three linear motifs. Notably, quadruple loss-of-function mutants from the non-ε group exhibit gain-of-function BR signaling phenotypes, suggesting a role for 14-3-3 proteins as overall negative regulators of the BR pathway. Collectively, our work provides further mechanistic and genetic evidence for the regulatory role of 14-3-3 proteins at various stages of the BR signaling cascade.
油菜素甾醇(BRs)是植物中重要的甾体激素,通过细胞膜信号复合物感知,该复合物由受体激酶 BRI1 和 SERK 家族共受体激酶组成。该复合物的激活导致抑制蛋白 BKI1 与受体分离,并通过糖原合酶激酶 3 蛋白 BIN2 对 BZR1/BES1 转录因子进行差异磷酸化。BR 信号通路的许多磷酸蛋白,包括 BRI1、SERKs、BKI1 和 BZR1/BES1,可以与 14-3-3 蛋白结合。在这项研究中,我们使用定量配体结合测定法来定义 BR 信号通路中的 BRI1 激酶结构域、BKI1 和拟南芥中的 BZR1 的 N 端结构域中的最小 14-3-3 结合位点。所有三个基序都需要磷酸化才能特异性地以中到低微摩尔亲和力与 14-3-3 结合。BR 信号组分在 14-3-3 非-ε亚组内显示出最小的同工型偏好。14-3-3λ 和 14-3-3 ω 同工型复合物晶体结构显示,BKI1 和 BZR1 作为典型的 II 型 14-3-3 线性基序结合。通过突变破坏磷酸肽结合位点的关键氨基酸会损害 14-3-3λ 与所有三个线性基序的相互作用。值得注意的是,非-ε 组的四重缺失功能突变体表现出 BR 信号功能获得表型,这表明 14-3-3 蛋白作为 BR 途径的整体负调节剂发挥作用。总之,我们的工作为 14-3-3 蛋白在 BR 信号级联的各个阶段的调节作用提供了进一步的机制和遗传证据。