Key Laboratory of Molecular Biology of Heilongjiang Province, College of Life Sciences, Heilongjiang University , Harbin 150080, China.
J Proteome Res. 2013 Nov 1;12(11):4931-50. doi: 10.1021/pr400177m. Epub 2013 Jun 25.
Understanding the mechanisms of plant salinity tolerance can facilitate plant engineering for enhanced salt stress tolerance. Sugar beet monosomic addition line M14 obtained from the intercross between Beta vulgaris L. and Beta corolliflora Zoss exhibits tolerance to salt stress. Here we report the salt-responsive characteristics of the M14 plants under 0, 200, and 400 mM NaCl conditions using quantitative proteomics approaches. Proteins from control and the salt treated M14 plants were separated using 2D-DIGE. Eighty-six protein spots representing 67 unique proteins in leaves and 22 protein spots representing 22 unique proteins in roots were identified. In addition, iTRAQ LC-MS/MS was employed to identify and quantify differentially expressed proteins under salt stress. Seventy-five differentially expressed proteins in leaves and 43 differentially expressed proteins in roots were identified. The proteins were mainly involved in photosynthesis, energy, metabolism, protein folding and degradation, and stress and defense. Moreover, gene transcription data obtained from the same samples were compared to the corresponding protein data. Thirteen proteins in leaves and 12 in roots showed significant correlation in gene expression and protein levels. These results suggest the important processes for the M14 tolerance to salt stress include enhancement of photosynthesis and energy metabolism, accumulation of osmolyte and antioxidant enzymes, and regulation of methionine metabolism and ion uptake/exclusion.
了解植物耐盐性的机制可以促进植物工程以提高耐盐胁迫能力。从糖甜菜(Beta vulgaris L.)和糖用甜菜(Beta corolliflora Zoss)杂交得到的单体附加系 M14 表现出对盐胁迫的耐受性。本研究采用定量蛋白质组学方法,在 0、200 和 400 mM NaCl 条件下,报告了 M14 植物的盐响应特性。用 2D-DIGE 分离对照和盐处理的 M14 植物的蛋白质。在叶片中鉴定到 86 个蛋白斑点,代表 67 种独特的蛋白质,在根中鉴定到 22 个蛋白斑点,代表 22 种独特的蛋白质。此外,采用 iTRAQ LC-MS/MS 鉴定和定量盐胁迫下差异表达的蛋白质。在叶片中鉴定到 75 种差异表达的蛋白质,在根中鉴定到 43 种差异表达的蛋白质。这些蛋白质主要参与光合作用、能量、代谢、蛋白质折叠和降解以及应激和防御。此外,还比较了来自相同样品的基因转录数据与相应的蛋白质数据。叶片中的 13 种蛋白质和根中的 12 种蛋白质在基因表达和蛋白质水平上均显示出显著相关性。这些结果表明,M14 耐盐性的重要过程包括增强光合作用和能量代谢、积累渗透调节剂和抗氧化酶、以及调节蛋氨酸代谢和离子摄取/排除。