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14-3-3 蛋白作为拟南芥油菜素内酯信号负调控因子的作用机制研究。

Mechanistic Insights into the Function of 14-3-3 Proteins as Negative Regulators of Brassinosteroid Signaling in Arabidopsis.

机构信息

Structural Plant Biology Laboratory, Department of Plant Sciences, University of Geneva, 30 Quai E. Ansermet, Geneva 1211, Switzerland.

出版信息

Plant Cell Physiol. 2024 Nov 13;65(10):1674-1688. doi: 10.1093/pcp/pcae056.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddb9/11558545/543debb14835/pcae056f1.jpg

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