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首页> 外文期刊>Frontiers in Plant Science >Comparative Proteomic Analysis of Soybean Leaves and Roots by iTRAQ Provides Insights into Response Mechanisms to Short-Term Salt Stress
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Comparative Proteomic Analysis of Soybean Leaves and Roots by iTRAQ Provides Insights into Response Mechanisms to Short-Term Salt Stress

机译:iTRAQ对大豆叶和根的比较蛋白质组学分析提供了对短期盐胁迫响应机制的见解

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Salinity severely threatens land use capability and crop yields worldwide. Understanding the mechanisms that protect soybeans from salt stress will help in the development of salt-stress tolerant leguminous plants. Here we initially analyzed the changes in malondialdehyde levels, the activities of superoxide dismutase and peroxidases, chlorophyll content, and Na~(+)/K~(+)ratios in leaves and roots from soybean seedlings treated with 200 mM NaCl at different time points. We found that the 200 mM NaCl treated for 12 h was optimal for undertaking a proteomic analysis on soybean seedlings. An iTRAQ-based proteomic approach was used to investigate the proteomes of soybean leaves and roots under salt treatment. These data are available via ProteomeXchange with the identifier PXD002851. In total, 278 and 440 proteins with significantly altered abundances were identified in leaves and roots of soybean, respectively. From these data, a total of 50 proteins were identified in the both tissues. These differentially expressed proteins (DEPs) were from 13 biological processes. Moreover, protein-protein interaction analysis revealed that proteins involved in metabolism, carbohydrate and energy metabolism, protein synthesis and redox homeostasis could be assigned to four high salt stress response networks. Furthermore, semi-quantitative RT-PCR analysis revealed that some of the proteins, such as a 14-3-3, MMK2, PP1, TRX-h, were also regulated by salt stress at the level of transcription. These results indicated that effective regulatory protein expression related to signaling, membrane and transport, stress defense and metabolism all played important roles in the short-term salt response of soybean seedlings.
机译:盐度严重威胁着全球的土地利用能力和农作物产量。了解保护大豆免受盐胁迫的机制,将有助于开发耐盐胁迫的豆科植物。在这里,我们首先分析了不同时间点用200 mM NaCl处理的大豆幼苗叶片和根中丙二醛水平,超氧化物歧化酶和过氧化物酶的活性,叶绿素含量以及Na〜(+)/ K〜(+)比率的变化。 。我们发现处理12 h的200 mM NaCl最适合对大豆幼苗进行蛋白质组学分析。基于iTRAQ的蛋白质组学方法用于研究盐处理下的大豆叶和根的蛋白质组。这些数据可通过ProteomeXchange获得,其标识符为PXD002851。总共,在大豆的叶和根中分别鉴定到278和440蛋白的丰度发生了明显变化。从这些数据中,在两个组织中总共鉴定出50种蛋白质。这些差异表达的蛋白质(DEP)来自13个生物学过程。此外,蛋白质-蛋白质相互作用分析表明,参与代谢,碳水化合物和能量代谢,蛋白质合成和氧化还原稳态的蛋白质可以分配给四个高盐胁迫响应网络。此外,半定量RT-PCR分析显示,某些蛋白质(例如14-3-3,MMK2,PP1,TRX-h)也受盐胁迫在转录水平上的调节。这些结果表明,与信号传导,膜和转运,胁迫防御和代谢有关的有效调节蛋白表达在大豆幼苗的短期盐反应中都起着重要作用。

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