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Proteome and Phosphoproteome Characterization Reveals New Response and Defense Mechanisms of Brachypodium distachyon Leaves under Salt Stress

机译:蛋白质组和磷酸化蛋白质组表征揭示了盐胁迫下短枝曲霉叶片的新应答和防御机制

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摘要

Salinity is a major abiotic stress affecting plant growth and development. Understanding the molecular mechanisms of salt response and defense in plants will help in efforts to improve the salt tolerance of crops. Brachypodium distachyon is a new model plant for wheat, barley, and several potential biofuel grasses. In the current study, proteome and phosphoproteome changes induced by salt stress were the focus. The Bd21 leaves were initially treated with salt in concentrations ranging from 80 to 320 mm and then underwent a recovery process prior to proteome analysis. A total of 80 differentially expressed protein spots corresponding to 60 unique proteins were identified. The sample treated with a median salt level of 240 mm and the control were selected for phosphopeptide purification using TiO2 microcolumns and LC-MS/MS for phosphoproteome analysis to identify the phosphorylation sites and phosphoproteins. A total of 1509 phosphoproteins and 2839 phosphorylation sites were identified. Among them, 468 phosphoproteins containing 496 phosphorylation sites demonstrated significant changes at the phosphorylation level. Nine phosphorylation motifs were extracted from the 496 phosphorylation sites. Of the 60 unique differentially expressed proteins, 14 were also identified as phosphoproteins. Many proteins and phosphoproteins, as well as potential signal pathways associated with salt response and defense, were found, including three 14-3-3s (GF14A, GF14B, and 14-3-3A) for signal transduction and several ABA signal-associated proteins such as ABF2, TRAB1, and SAPK8. Finally, a schematic salt response and defense mechanism in B. distachyon was proposed.
机译:盐度是影响植物生长发育的主要非生物胁迫。了解植物对盐的反应和防御的分子机制将有助于提高作物的耐盐性。 Brachypodium distachyon是一种用于小麦,大麦和几种潜在生物燃料草的新型植物。在当前的研究中,盐胁迫引起的蛋白质组和磷酸化蛋白质组变化是研究的重点。 Bd21叶片最初用浓度为80至320 mm的盐处理,然后在进行蛋白质组分析之前进行了恢复过程。鉴定出总共80个差异表达的蛋白质斑点,对应于60个独特的蛋白质。使用TiO2微柱和LC-MS / MS对中值盐含量为240 mm的样品和对照样品进行磷酸肽纯化,以进行磷酸化蛋白质组分析,以鉴定磷酸化位点和磷酸化蛋白。总共鉴定出1509个磷蛋白和2839个磷酸化位点。其中,包含496个磷酸化位点的468个磷蛋白在磷酸化水平上显示出显着变化。从496个磷酸化位点中提取了9个磷酸化基序。在60种独特的差异表达蛋白中,还有14种也被鉴定为磷蛋白。发现了许多蛋白质和磷蛋白以及与盐反应和防御相关的潜在信号途径,包括用于信号转导的三个14-3-3(GF14A,GF14B和14-3-3A)和一些与ABA信号相关的蛋白质例如ABF2,TRAB1和SAPK8。最后,提出了示意性盐沼中盐反应和防御机制。

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