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Comparative proteomic analysis of okra ( Abelmoschus esculentus L . ) seedlings under salt stress

机译:盐胁迫下黄秋葵幼苗的蛋白质组学比较研究。

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Salinization seriously threatens land use efficiency and crop yields across the world. Understanding the mechanisms plants use to protect against salt stress will help breeders develop salt-tolerant vegetable crops. Okra (Abelmoschus esculentus L.) is an important vegetable crop of the mallow family, which is now cultivated in warm regions worldwide. To understand the effects of salt stress on the protein level of okra, a comparative proteomic analysis of okra seedlings grown in the presence of 0 or 300?mmol?L??1 NaCl treatment was performed using an integrated approach of Tandem Mass Tag labeling and LC-MS/MS integrated approach. A total of 7179 proteins were identified in this study, for which quantitative information was available for 5774 proteins. In the NaCl/control comparison group, there were 317 differentially expressed proteins (DEPs), of which 165 proteins were upregulated and 152 proteins downregulated in the presence of NaCl. Based on the above data, we carried out a systematic bioinformatics analysis of proteins with information, including protein annotation, domain characteristics, functional classification, and pathway enrichment. Enriched gene ontology and Kyoto Encyclopedia of Genes and Genomes pathway analysis showed that the DEPs were most strongly associated with “response to stress” and “protein processing in endoplasmic reticulum”. Furthermore, several heat shock proteins were identified as DEPs. This information provides a reference direction for further research on the okra proteome in the downstream of the salt stress response, with our data revealing that the responses of okra to salt stress involves by various pathways.
机译:盐碱化严重威胁着全世界的土地利用效率和农作物产量。了解植物用于防止盐胁迫的机制将有助于育种者发展耐盐蔬菜作物。黄秋葵(Abelmoschus esculentus L.)是锦葵科的重要蔬菜作物,现已在全球温暖的地区种植。为了了解盐胁迫对秋葵蛋白质水平的影响,采用串联质量标签标记和结合的综合方法对在0或300?mmol?L?1 NaCl处理下生长的秋葵幼苗进行了蛋白质组学比较分析。 LC-MS / MS集成方法。这项研究共鉴定了7179种蛋白质,其中5774种蛋白质的定量信息可用。在NaCl /对照组中,存在317个差异表达蛋白(DEP),其中有165个蛋白被上调,而152个蛋白在NaCl存在下被下调。基于以上数据,我们对蛋白质进行了系统的生物信息学分析,并提供了包括蛋白质注释,结构域特征,功能分类和途径富集在内的信息。丰富的基因本体论和《京都议定书》的基因与基因组百科全书通路分析表明,DEP与“对应激的反应”和“内质网中的蛋白质加工”密切相关。此外,几种热激蛋白被鉴定为DEP。该信息为进一步研究盐胁迫响应下游的秋葵蛋白质组提供了参考方向,我们的数据表明秋葵对盐胁迫的响应涉及多种途径。

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