Northeast Forestry University, Harbin 150040, China.
Int J Mol Sci. 2017 Oct 18;18(10):2090. doi: 10.3390/ijms18102090.
Mitogen-activated protein kinase (MAPK) is one of the factors of cascade reactions affecting responses to signal pathway of environmental stimuli. Throughout the life of plants, MAPK family members participate in signal transduction pathways and regulate various intracellular physiological and metabolic reactions. To gain insights into regulatory function of MAPK kinase (MAPKK) in under salt stress, we obtained full-length cDNA of and analyzed different expression levels of gene in leaves, stems, and root organs. The relationship between PtMAPKK4 and salt stress was studied by detecting expression characteristics of mRNA under 150 mM NaCl stress using real-time quantitative polymerase chain reaction. The results showed that expression of increased under salt (NaCl) stress in leaves but initially reduced and then increased in roots. Thus, salt stress failed to induce PtMAPKK4 expression in stems. PtMAPKK4 possibly participates in regulation of plant growth and metabolism, thereby improving its salt tolerance. We used strain INVScI to verify subcellular localization of PtMAPKK4 kinase. The yeast strains containing pYES2-PtMAPKK4-GFP plasmid expressed GFP fusion proteins under the induction of d-galactose, and the products were located in nucleus. These results were consistent with network prediction and confirmed location of PtMAPKK4 enzyme in the nucleus. We tested NaCl tolerance in transgenic tobacco lines overexpressing under the control of 35S promoter at germination stage to detect salt tolerance function of PtMAPKK4. Compared withK326 (a wild-type tobacco), lines overexpressing showed a certain degree of improvement in tolerance, germination, and growth. NaCl inhibited growth of overexpressed line and K326 at the seedling stage. However, statistical analysis showed longer root length, higher fresh weight, and lower MDA content in transgenic lines in comparison with that in K326.
丝裂原活化蛋白激酶(MAPK)是影响环境刺激信号通路反应的级联反应因素之一。在植物的整个生命周期中,MAPK 家族成员参与信号转导途径并调节各种细胞内的生理和代谢反应。为了深入了解 MAPK 激酶(MAPKK)在盐胁迫下的调控功能,我们获得了全长 cDNA,并分析了基因在叶片、茎和根器官中的不同表达水平。通过实时定量聚合酶链反应检测 150mM NaCl 胁迫下 mRNA 的表达特征,研究了 PtMAPKK4 与盐胁迫的关系。结果表明,盐(NaCl)胁迫下叶片中 PtMAPKK4 的表达增加,但根中最初减少,然后增加。因此,盐胁迫未能诱导茎中 PtMAPKK4 的表达。PtMAPKK4 可能参与植物生长和代谢的调节,从而提高其耐盐性。我们使用 菌株 INVScI 验证 PtMAPKK4 激酶的亚细胞定位。含有 pYES2-PtMAPKK4-GFP 质粒的酵母菌株在 d-半乳糖的诱导下表达 GFP 融合蛋白,产物位于细胞核中。这些结果与网络预测一致,并证实了 PtMAPKK4 酶在细胞核中的位置。我们在萌发阶段使用 35S 启动子控制下过表达 PtMAPKK4 的转基因烟草系检测 PtMAPKK4 的耐盐功能。与 K326(野生型烟草)相比,过表达 PtMAPKK4 的系在耐盐性、萌发和生长方面表现出一定程度的改善。NaCl 抑制了过表达系和 K326 在幼苗阶段的生长。然而,与 K326 相比,统计分析显示转基因系的根长较长、鲜重较高、MDA 含量较低。