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基于等重标记相对和绝对定量技术(iTRAQ)的定量蛋白质组学分析鉴定盐胁迫响应蛋白。

Identification of Early Salinity Stress-Responsive Proteins in by isobaric tags for relative and absolute quantitation (iTRAQ)-Based Quantitative Proteomic Analysis.

机构信息

Key Laboratory of Hydrobiology in Liaoning Province's Universities, Dalian Ocean University, Dalian 116021, China.

College of fisheries and life science, Dalian Ocean University, Dalian 116021, China.

出版信息

Int J Mol Sci. 2019 Jan 30;20(3):599. doi: 10.3390/ijms20030599.

Abstract

Salt stress is one of the most serious abiotic factors that inhibit plant growth. 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 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 and potentially contributes to developing strategies to improve stress resilience.

摘要

盐胁迫是抑制植物生长的最严重非生物因素之一。 由于其耐受极端盐胁迫的能力很强,因此被认为是研究应激反应的模式生物。本研究采用基于相对和绝对定量同位素标记技术(iTRAQ)的蛋白质组学方法,分析了 在盐胁迫早期响应过程中的蛋白质组,并鉴定了差异丰度蛋白(DAP)。在盐处理的样品中鉴定出了 141 个 DAP,包括 3 h 和 24 h 盐胁迫后分别上调的 75 个和下调的 66 个 DAP。对 DAP 进行注释和分类,归入基因本体论功能组。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,在每个时间点构建了包含 33 个和 52 个节点的 DAP 调控蛋白⁻蛋白相互作用(PPI)网络,表明光合作用和 ATP 合成对早期盐响应途径的调节至关重要。通过定量实时聚合酶链反应(qRT-PCR)对 5 个 DAP 的相应转录水平进行了定量。这些结果概述了 对盐胁迫的系统分子响应。本研究揭示了 在早期耐盐中的复杂调控机制,并可能有助于制定提高抗应激能力的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f248/6386831/313cd918d924/ijms-20-00599-g001.jpg

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