College of Plant Science, Jilin University, Changchun 130062, China.
Key Laboratory of Herbage & Endemic Crop Biology of Ministry of Education, School of Life Sciences, Inner Mongolia University, Hohhot 010000, China.
J Hazard Mater. 2024 Nov 5;479:135485. doi: 10.1016/j.jhazmat.2024.135485. Epub 2024 Aug 15.
Aluminum (Al) toxicity adversely impacts soybean (Glycine max) growth in acidic soil. Reversible protein phosphorylation plays an important role in adapting to adverse environmental conditions by regulating multiple physiological processes including signal transduction, energy coupling and metabolism adjustment in higher plant. This study aimed to reveal the Al-responsive phosphoproteins to understand their putative function and involvement in the regulation of Al resistance in soybean root. We used immobilized metal affinity chromatography to enrich the key phosphoproteins from soybean root apices at 0, 4, or 24 h Al exposure. These phosphoproteins were detected using liquid chromatography-tandem mass spectrometry measurement, verified by parallel reaction monitoring (PRM), and functionally characterized via overexpression in soybean hairy roots. A total of 638 and 686 phosphoproteins were identified as differentially enriched between the 4-h and 0-h, and the 24-h and 0-h Al treatment comparison groups, respectively. Typically, the phosphoproteins involved in biological processes including cell wall modification, and RNA and protein metabolic regulation displayed patterns of decreasing enrichment (clusters 3, 5 and 6), however, the phosphoproteins involved in the transport and metabolic processes of various substrates, and signal transduction pathways showed increased enrichment after 24 h of Al treatment. The enrichment of phosphoproteins in organelle organization bottomed after 4 h of Al treatment (cluster 1). Next, we selected 26 phosphoproteins from the phosphoproteomic profiles, assessed their enrichment status using PRM, and detected enrichment patterns similar to those observed via phosphoproteomic analysis. Among them, 15 phosphoproteins were found to reduce the accumulation of Al and callose in Al-stressed soybean root apices when their corresponding genes were individually overexpressed in soybean hairy roots. In summary, the findings of this study facilitated a comprehensive understanding of the protein phosphorylation events involved in Al resistance responses and revealed some critical phosphoproteins that enhance Al resistance in soybean roots.
铝(Al)毒性会对酸性土壤中的大豆(Glycine max)生长产生不利影响。可逆蛋白磷酸化在高等植物适应不利环境条件中起着重要作用,通过调节包括信号转导、能量偶联和代谢调节在内的多个生理过程来发挥作用。本研究旨在揭示铝响应的磷酸化蛋白,以了解它们在调节大豆根系耐铝性中的潜在功能和作用。我们使用固定金属亲和层析从大豆根尖在 0、4 或 24 小时铝暴露下富集关键的磷酸化蛋白。使用液相色谱-串联质谱法测量这些磷酸化蛋白,通过平行反应监测(PRM)验证,并通过在大豆毛状根中过表达进行功能表征。在 4 小时和 0 小时、24 小时和 0 小时铝处理比较组之间,分别鉴定出 638 个和 686 个差异富集的磷酸化蛋白。通常,参与细胞壁修饰以及 RNA 和蛋白质代谢调节等生物过程的磷酸化蛋白显示出逐渐减少的富集模式(簇 3、5 和 6),然而,参与各种底物的运输和代谢过程以及信号转导途径的磷酸化蛋白在 24 小时铝处理后显示出增加的富集。细胞器组织的磷酸化蛋白在 4 小时铝处理后达到富集峰值(簇 1)。接下来,我们从磷酸蛋白质组学图谱中选择了 26 个磷酸化蛋白,使用 PRM 评估它们的富集状态,并检测到与磷酸蛋白质组学分析相似的富集模式。其中,当它们各自的基因在大豆毛状根中过表达时,15 个磷酸化蛋白被发现减少了铝和胼胝质在铝胁迫下大豆根尖的积累。综上所述,本研究的结果有助于全面了解参与耐铝性反应的蛋白磷酸化事件,并揭示了一些增强大豆根系耐铝性的关键磷酸化蛋白。