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The Phosphoproteomic Response of Okra (Abelmoschus esculentus L.) Seedlings to Salt Stress

机译:黄秋葵(Abelmoschus esculentus L.)幼苗对盐胁迫的磷酸化蛋白质组学响应

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摘要

Soil salinization is a major environmental stresses that seriously threatens land use efficiency and crop yields worldwide. Although the overall response of plants to NaCl has been well studied, the contribution of protein phosphorylation to the detoxification and tolerance of NaCl in okra (Abelmoschus esculentus L.) seedlings is unclear. The molecular bases of okra seedlings’ responses to 300 mM NaCl stress are discussed in this study. Using a combination of affinity enrichment, tandem mass tag (TMT) labeling and high-performance liquid chromatography–tandem mass spectrometry analysis, a large-scale phosphoproteome analysis was performed in okra. A total of 4341 phosphorylation sites were identified on 2550 proteins, of which 3453 sites of 2268 proteins provided quantitative information. We found that 91 sites were upregulated and 307 sites were downregulated in the NaCl/control comparison group. Subsequently, we performed a systematic bioinformatics analysis including gene ontology annotation, domain annotation, subcellular localization, and Kyoto Encyclopedia of Genes and Genomes pathway annotation. The latter revealed that the differentially expressed proteins were most strongly associated with ‘photosynthesis antenna proteins’ and ‘RNA degradation’. These differentially expressed proteins probably play important roles in salt stress responses in okra. The results should help to increase our understanding of the molecular mechanisms of plant post-translational modifications in response to salt stress.
机译:土壤盐渍化是主要的环境压力,严重威胁着全球的土地利用效率和农作物产量。尽管已经对植物对NaCl的总体反应进行了深入研究,但尚不清楚蛋白质磷酸化对秋葵(Abelmoschus esculentus L.)幼苗中NaCl的解毒和耐受性的贡献。本研究讨论了黄秋葵幼苗对300 mM NaCl胁迫的响应的分子基础。通过亲和力富集,串联质谱标签(TMT)标记和高效液相色谱-串联质谱分析相结合,在秋葵中进行了大规模的磷酸化蛋白质组分析。在2550种蛋白质上共鉴定到4341个磷酸化位点,其中2268个蛋白质的3453个位点提供了定量信息。我们发现在NaCl /对照组中,有91个位点被上调,而有307个位点被下调。随后,我们进行了系统的生物信息学分析,包括基因本体标注,域标注,亚细胞定位以及《京都议定书》的基因和基因组途径标注。后者表明差异表达的蛋白质与“光合作用触角蛋白质”和“ RNA降解”密切相关。这些差异表达的蛋白质可能在秋葵的盐胁迫响应中起重要作用。结果应有助于增进我们对植物对盐胁迫的翻译后修饰的分子机制的了解。

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