PDF HTML阅读 XML下载 导出引用 引用提醒 花生叶片蛋白组对UV-B辐射增强的响应 DOI: 10.5846/stxb201302030223 作者: 作者单位: 三峡库区生态环境教育部重点实验室,台州学院生态研究所,三峡库区生态环境教育部重点实验室,中国科学院植物研究所植被与环境变化国家重点实验室 作者简介: 通讯作者: 中图分类号: 基金项目: 国家自然科学基金资助项目(30670334,31270461);浙江省教育厅科研项目(Y201223322);中央高校基本科研业务费专项资金资助项目(XDJK2011D009) A proteomic analysis of Arachis hypogaea leaf in responses to enhanced ultraviolet-B radiation Author: Affiliation: MOE Key Laboratory of Eco-environments of Three Gorges Reservoir Region,School of Life Science,Southwest University,Institute of Ecology,Taizhou University,MOE Key Laboratory of Eco-environments of Three Gorges Reservoir Region,School of Life Science,Southwest University,State Key Laboratory of Vegetation and Environmental Change,Institute of Botany,Chinese Academy of Sciences Fund Project: 摘要 | 图/表 | 访问统计 | 参考文献 | 相似文献 | 引证文献 | 资源附件 | 文章评论 摘要:为揭示UV-B辐射增强处理降低花生光合速率和花生抵御UV-B辐射增强的分子机制,应用蛋白质双向电泳与质谱联用技术对自然光环境下补增UV-B辐射(54 μW/cm2)处理24h的苗期花生叶片差异表达蛋白质变化进行了分析。结果表明:补增UV-B处理下,花生叶片中共检测到丰度变化在2.5倍以上的差异表达蛋白点39个(其中22种蛋白质表达下调,17种表达上调),经过MALDI-TOF-TOF分析及数据库检索,成功鉴定出其中的27种蛋白质。被鉴定的27种蛋白质按其功能大致可归为8类,第Ⅰ类:光合作用相关的蛋白质,包括质体蓝素、1,5-二磷酸核酮糖羧化酶小亚基、放氧复合物增强子蛋白1、PsbP结构域蛋白6和果糖二磷酸醛缩酶;第Ⅱ类:糖代谢相关蛋白质,包括苹果酸脱氢酶;第Ⅲ类:能量合成相关蛋白质,包括ATP合酶;第Ⅳ类:氨基酸代谢相关蛋白质,包括半胱氨酸合成酶;第Ⅴ类:蛋白质加工相关蛋白质,包括热激蛋白;第Ⅵ类:蛋白质翻译相关蛋白质,包括核糖体循环因子;第Ⅶ类:防御相关蛋白质,包括几丁质酶、过氧化物酶、Cu-Zn超氧化物歧化酶、二羟肉桂酸3-O-转甲基酶和类萌发素蛋白;第Ⅷ类,未知功能蛋白质。这些研究结果为进一步研究花生抵御UV-B辐射的分子机理提供了有意义的线索。 Abstract:Ultraviolet-B (UV-B, 280-320 nm) constitutes a minor part of the solar spectrum, which can be absorbed by stratospheric ozone layer. However, a global depletion of the ozone layer, largely due to the release of man-made chlorofluorocarbons, has resulted in an increase of ground-level solar UV-B radiation. UV-B can influence plant processes, either through direct damage or via various regulatory effects. Many researches have warned that excessive UV-B radiation can harm living organisms by damaging DNA, proteins, lipids, and membranes and consequently affecting plant growth, development, morphology, and productivity. Two-dimensional polyacrylamide gel electrophoresis (2-D PAGE) is a powerful technique for resolving hundreds of proteins in parallel. Combined with mass spectrometry (MS), it allows rapid and reliable protein identification. In recent years, proteomic-based technologies have been successfully applied to systematic studies of the stress responses many plant species, including Arabidopsis, soybean, rice, wheat, barley, potato, tomato, and many others. A wide range of abiotic stresses have been examined, such as drought, nutrition deficiency, temperature, oxidative stress, herbicides, wounding, anoxia, salt, and heavy metals. These investigations have provided a wealth of important information on the physiological processes involved in plant stress responses. To explore the molecular mechanisms of the decreased photosynthetic rate and the resistance of peanut (Arachis hypogaea) when exposed to enhanced UV-B radiation, 2-D PAGE and MS were used to identify the differentially-expressed proteins in peanut seedling leaves in response to supplementary UV-B radiation (54 μW/cm2) for 24 h. A total of 39 protein spots were differentially expressed by at least 2.5 fold compared with the controls (22 proteins were down-regulated and 17 were up-regulated) after treatment with supplementary UV-B radiation. Of those protein spots, 27 were successfully identified by MALDI TOF/TOF MS after a database search. Those 27 proteins could be classified into eight categories according to their functions: class Ⅰ, photosynthesis (plastocyanin, ribulose-1,5-bisphosphate carboxylase small subunit, oxygen-evolving enhancer protein 1, PsbP domain-containing protein 6, and fructose-bisphosphate aldolase); class Ⅱ, carbohydrate metabolism (malate dehydrogenase); class Ⅲ, energy synthesis (ATP synthase); class Ⅳ, amino acid biosynthesis (cysteine synthase); class Ⅴ, protein biosynthesis (ribosome recycling factor); class Ⅵ, protein processing (heat shock proteins); class Ⅶ, defense responses (chitinase, peroxidase, Cu-Zn SOD, caffeic acid 3-O-methyltransferase, and germin-like protein); class Ⅷ, unknown proteins. In conclusion, we hypothesized that the enhanced UV-B radiation caused a decrease in the photosynthesis rate of peanut leaves mainly via three mechanisms. First, enhanced UV-B may down-regulate the expression of ribosome recycling factor, which caused a decrease in the expression of subunit PsbP in photosystem Ⅱ, thus destroying the thylakoid membrane structure. Second, the reduced plastocyanin expression may have induced a decrease in photosynthetic electron transport efficiency. Third, the down-regulation of ribulose-1,5-bisphosphate carboxylase and fructose-1,6-bisphosphate aldolase resulted in a decrease in carbon assimilation. At the same time, peanut may also enhance its resistance to UV-B stress by increasing the expressions of antioxidant enzymes and non-enzymatic antioxidants, germin-like proteins, pathogenesis-related proteins, and heat shock proteins. These results provide important information for understanding the molecular mechanisms by which A. hypogaea responds to elevated UV-B stress. 参考文献 相似文献 引证文献