Lee Justin, Eschen-Lippold Lennart, Lassowskat Ines, Böttcher Christoph, Scheel Dierk
Department of Stress and Developmental Biology, Leibniz Institute of Plant Biochemistry Halle/Saale, Germany.
Department of Stress and Developmental Biology, Leibniz Institute of Plant Biochemistry Halle/Saale, Germany ; Federal Research Centre for Cultivated Plants, Ecological Chemistry, Julius Kühn Institute, Plant Analysis and Stored Product Protection Berlin, Germany.
Front Plant Sci. 2015 Oct 29;6:940. doi: 10.3389/fpls.2015.00940. eCollection 2015.
Mitogen-activated protein kinase (MAPK) cascades are conserved eukaryote signaling modules where MAPKs, as the final kinases in the cascade, phosphorylate protein substrates to regulate cellular processes. While some progress in the identification of MAPK substrates has been made in plants, the knowledge on the spectrum of substrates and their mechanistic action is still fragmentary. In this focused review, we discuss the biological implications of the data in our original paper (Sustained mitogen-activated protein kinase activation reprograms defense metabolism and phosphoprotein profile in Arabidopsis thaliana; Frontiers in Plant Science 5: 554) in the context of related research. In our work, we mimicked in vivo activation of two stress-activated MAPKs, MPK3 and MPK6, through transgenic manipulation of Arabidopsis thaliana and used phosphoproteomics analysis to identify potential novel MAPK substrates. Here, we plotted the identified putative MAPK substrates (and downstream phosphoproteins) as a global protein clustering network. Based on a highly stringent selection confidence level, the core networks highlighted a MAPK-induced cellular reprogramming at multiple levels of gene and protein expression-including transcriptional, post-transcriptional, translational, post-translational (such as protein modification, folding, and degradation) steps, and also protein re-compartmentalization. Additionally, the increase in putative substrates/phosphoproteins of energy metabolism and various secondary metabolite biosynthesis pathways coincides with the observed accumulation of defense antimicrobial substances as detected by metabolome analysis. Furthermore, detection of protein networks in phospholipid or redox elements suggests activation of downstream signaling events. Taken in context with other studies, MAPKs are key regulators that reprogram cellular events to orchestrate defense signaling in eukaryotes.
丝裂原活化蛋白激酶(MAPK)级联是保守的真核生物信号模块,其中MAPK作为级联中的最终激酶,磷酸化蛋白质底物以调节细胞过程。虽然植物在MAPK底物的鉴定方面已经取得了一些进展,但关于底物谱及其作用机制的知识仍然支离破碎。在这篇重点综述中,我们结合相关研究讨论了我们原论文(《持续的丝裂原活化蛋白激酶激活重编程拟南芥的防御代谢和磷酸化蛋白质谱》;《植物科学前沿》5:554)中数据的生物学意义。在我们的工作中,我们通过对拟南芥进行转基因操作模拟了两种应激激活的MAPK,即MPK3和MPK6的体内激活,并使用磷酸化蛋白质组学分析来鉴定潜在的新型MAPK底物。在这里,我们将鉴定出的假定MAPK底物(和下游磷酸化蛋白质)绘制成一个全局蛋白质聚类网络。基于高度严格的选择置信水平,核心网络突出了MAPK在基因和蛋白质表达的多个水平上诱导的细胞重编程,包括转录、转录后、翻译、翻译后(如蛋白质修饰、折叠和降解)步骤,以及蛋白质重新定位。此外,能量代谢和各种次生代谢物生物合成途径的假定底物/磷酸化蛋白质的增加与代谢组分析检测到的防御抗菌物质的积累相一致。此外,对磷脂或氧化还原元件中蛋白质网络的检测表明下游信号事件被激活。结合其他研究来看,MAPK是关键的调节因子,可重编程细胞事件以协调真核生物中的防御信号传导。