首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Identification of Early Salinity Stress-Responsive Proteins in Dunaliella salina by isobaric tags for relative and absolute quantitation (iTRAQ)-Based Quantitative Proteomic Analysis
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Identification of Early Salinity Stress-Responsive Proteins in Dunaliella salina by isobaric tags for relative and absolute quantitation (iTRAQ)-Based Quantitative Proteomic Analysis

机译:基于等量和绝对定量(iTRAQ)的定量蛋白质组学分析的等压标记鉴定杜氏盐藻中的早期盐度胁迫响应蛋白

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摘要

Salt stress is one of the most serious abiotic factors that inhibit plant growth. Dunaliella salina has been recognized as a model organism for stress response research due to its high capacity to tolerate extreme salt stress. A proteomic approach based on isobaric tags for relative and absolute quantitation (iTRAQ) was used to analyze the proteome of D. salina during early response to salt stress and identify the differentially abundant proteins (DAPs). A total of 141 DAPs were identified in salt-treated samples, including 75 upregulated and 66 downregulated DAPs after 3 and 24 h of salt stress. DAPs were annotated and classified into gene ontology functional groups. The Kyoto Encyclopedia of Genes and Genomes pathway analysis linked DAPs to tricarboxylic acid cycle, photosynthesis and oxidative phosphorylation. Using search tool for the retrieval of interacting genes (STRING) software, regulatory protein–protein interaction (PPI) networks of the DAPs containing 33 and 52 nodes were built at each time point, which showed that photosynthesis and ATP synthesis were crucial for the modulation of early salinity-responsive pathways. The corresponding transcript levels of five DAPs were quantified by quantitative real-time polymerase chain reaction (qRT-PCR). These results presented an overview of the systematic molecular response to salt stress. This study revealed a complex regulatory mechanism of early salt tolerance in D. salina and potentially contributes to developing strategies to improve stress resilience.
机译:盐胁迫是抑制植物生长的最严重的非生物因素之一。杜氏盐藻由于具有很高的耐极端盐胁迫的能力,因此被公认为是胁迫反应研究的模式生物。一种基于等压标记的相对和绝对定量蛋白质组学方法(iTRAQ)用于分析盐胁迫早期响应过程中盐藻的蛋白质组,并鉴定差异丰富的蛋白质(DAP)。盐处理样品中共鉴定出141种DAP,包括盐胁迫3和24小时后上调的75种DAP和66种下调的DAP。注释DAP并将其分类为基因本体功能组。京都基因与基因组百科全书途径分析将DAP与三羧酸循环,光合作用和氧化磷酸化联系起来。使用搜索工具检索相互作用基因(STRING)软件,在每个时间点分别建立了包含33和52个节点的DAP的调节蛋白-蛋白相互作用(PPI)网络,这表明光合作用和ATP合成对于调节至关重要盐度响应的早期途径。通过定量实时聚合酶链反应(qRT-PCR)量化了五个DAP的相应转录水平。这些结果概述了对盐胁迫的系统分子反应。这项研究揭示了盐藻的早期耐盐性的复杂调控机制,并可能有助于开发提高抗逆力的策略。

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