Co-Innovation Center for Modern Production Technology of Grain Crops/Jiangsu Key Laboratory of Crop Genetics and Physiology, College of Bioscience and Biotechnology, Yangzhou University, Yangzhou, 225009, China.
Joint International Research Laboratory of Agriculture and Agri-Product Safety of Ministry of Education of China, Yangzhou University, Yangzhou, China.
Protoplasma. 2020 Jan;257(1):43-59. doi: 10.1007/s00709-019-01419-6. Epub 2019 Jul 29.
High temperature (HT) is one of the major environmental factors which limits plant growth and yield. The mitogen-activated protein kinase (MAPK) plays vital roles in environmental stress responses. However, the mechanisms triggered by MAPKs in plants in response to HT are still extremely limited. In this study, the proteomic data of differences between SlMPK1 RNA-interference mutant (SlMPK1i) and wild type and of tomato (Solanum lycopersicum) plants under HT stress using isobaric tags for relative and absolute quantitation (iTRAQ) was re-analyzed in depth. In total, 168 differently expressed proteins (DEPs) were identified in response to HT stress, including 38 DEPs only found in wild type, and 84 DEPs specifically observed in SlMPK1i after HT treatment. The majority of higher expression of 84 DEPs were annotated into photosynthesis, oxidation-reduction process, protein folding, translation, proteolysis, stress response, and amino acid biosynthetic process. More importantly, SlMPK1-mediated photosynthesis was confirmed by the physiological characterization of SlMPK1i with a higher level of photosynthetic capacity under HT stress. Overall, the results reveal a set of potential candidate proteins helping to further understand the intricate regulatory network regulated by SlMPK1 in response to HT.
高温(HT)是限制植物生长和产量的主要环境因素之一。丝裂原活化蛋白激酶(MAPK)在环境胁迫响应中发挥着重要作用。然而,MAPK 在植物中响应 HT 所触发的机制仍然非常有限。在这项研究中,使用相对和绝对定量同位素标记(iTRAQ)对 SlMPK1 RNA 干扰突变体(SlMPK1i)和野生型番茄(Solanum lycopersicum)在 HT 胁迫下的蛋白质组学数据进行了深入的重新分析。总共鉴定出 168 个对 HT 胁迫有差异表达的蛋白质(DEPs),包括仅在野生型中发现的 38 个 DEPs,以及在 HT 处理后 SlMPK1i 中特异性观察到的 84 个 DEPs。84 个 DEPs 的大多数高表达被注释为光合作用、氧化还原过程、蛋白质折叠、翻译、蛋白水解、应激反应和氨基酸生物合成过程。更重要的是,通过 SlMPK1i 的生理特征证实了 SlMPK1 介导的光合作用,SlMPK1i 在 HT 胁迫下具有更高的光合作用能力。总体而言,这些结果揭示了一组潜在的候选蛋白,有助于进一步了解 SlMPK1 响应 HT 调节的复杂调控网络。