Key Laboratory of Molecular Biology of Heilongjiang Province, College of Life Sciences, Heilongjiang University, Harbin 150080, China.
J Plant Physiol. 2012 Jun 15;169(9):839-50. doi: 10.1016/j.jplph.2012.01.023. Epub 2012 Apr 10.
Sugar beet monosomic addition line M14 displays interesting phenotypes such as apomixis and salt stress tolerance. Here we reported proteomic and transcriptomic analysis of M14 leaves and roots under 500mM NaCl treatment for seven days. Proteins from control and treated samples were extracted and separated using two-dimensional difference gel electrophoresis (2D-DIGE). A total of 40 protein spots from leaf gels and 36 protein spots from root gels exhibited significant changes. Using mass spectrometry and database searching, 38 unique proteins in leaves and 29 unique proteins in roots were identified. The proteins included those involved in metabolism, protein folding, photosynthesis, and protein degradation. In addition, cDNA libraries of differentially expressed genes were constructed using suppression subtractive hybridization (SSH). Fifty-eight unigenes including 14 singletons and 44 contigs were obtained. Some salt-responsive genes were identified to function in metabolism, photosynthesis, stress and defense, energy, protein synthesis and protein degradation. This research has revealed candidate genes and proteins for detailed functional characterization, and set the stage for further investigation of the salt tolerance mechanisms in sugar beet.
甜菜单体附加系 M14 表现出有趣的表型,如无融合生殖和耐盐性。在这里,我们报道了 M14 叶片和根系在 500mM NaCl 处理 7 天后的蛋白质组学和转录组学分析。用二维差异凝胶电泳(2D-DIGE)从对照和处理样品中提取和分离蛋白质。从叶胶中得到了 40 个蛋白斑点,从根胶中得到了 36 个蛋白斑点,这些斑点显示出明显的变化。利用质谱和数据库搜索,在叶片中鉴定出 38 种独特的蛋白质,在根中鉴定出 29 种独特的蛋白质。这些蛋白质包括参与代谢、蛋白质折叠、光合作用和蛋白质降解的蛋白质。此外,还利用抑制性消减杂交(SSH)构建了差异表达基因的 cDNA 文库。获得了 58 个基因,包括 14 个单基因和 44 个基因簇。一些盐响应基因被鉴定为在代谢、光合作用、应激和防御、能量、蛋白质合成和蛋白质降解中发挥作用。这项研究揭示了候选基因和蛋白质,为详细的功能特征分析奠定了基础,并为进一步研究甜菜的耐盐机制奠定了基础。