Jin Xiao-Lin, Ma Cui-Lan, Yang Lin-Tong, Chen Li-Song
Institute of Plant Nutritional Physiology and Molecular Biology, College of Resources and Environment, Fujian Agriculture and Forestry University, Fuzhou 350002, China; College of Horticulture, Fujian Agriculture and Forestry University, Fuzhou 350002, China.
Institute of Plant Nutritional Physiology and Molecular Biology, College of Resources and Environment, Fujian Agriculture and Forestry University, Fuzhou 350002, China; Fujian Provincial Key Laboratory of Soil Environmental Health and Regulation, Fuzhou 350002, China.
J Plant Physiol. 2016 Jul 1;198:103-15. doi: 10.1016/j.jplph.2016.04.011. Epub 2016 May 4.
Seedlings of Ponkan (Citrus reticulata) were irrigated with nutrient solution containing 0 (Mg-deficiency) or 1mM MgSO4 (control) every two day for 16 weeks. Thereafter, we examined magnesium (Mg)-deficiency-induced changes in leaf and root gas exchange, total soluble proteins and gene expression. Mg-deficiency lowered leaf CO2 assimilation, and increased leaf dark respiration. However, Mg-deficient roots had lower respiration. Total soluble protein level was not significantly altered by Mg-deficiency in roots, but was lower in Mg-deficient leaves than in controls. Using cDNA-AFLP, we obtained 70 and 71 differentially expressed genes from leaves and roots. These genes mainly functioned in signal transduction, stress response, carbohydrate and energy metabolism, cell transport, cell wall and cytoskeleton metabolism, nucleic acid, and protein metabolisms. Lipid metabolism (Ca(2+) signals)-related Mg-deficiency-responsive genes were isolated only from roots (leaves). Although little difference existed in the number of Mg-deficiency-responsive genes between them both, most of these genes only presented in Mg-deficient leaves or roots, and only four genes were shared by them both. Our data clearly demonstrated that Mg-deficiency-induced alterations of physiology and gene expression greatly differed between leaves and roots. In addition, we focused our discussion on the causes for photosynthetic decline in Mg-deficient leaves and the responses of roots to Mg-deficiency.
每隔一天用含0(缺镁)或1mM MgSO4(对照)的营养液灌溉椪柑(Citrus reticulata)幼苗,持续16周。此后,我们检测了缺镁诱导的叶片和根系气体交换、总可溶性蛋白及基因表达的变化。缺镁降低了叶片的CO2同化作用,并增加了叶片的暗呼吸。然而,缺镁的根系呼吸作用较低。缺镁对根系总可溶性蛋白水平没有显著影响,但缺镁叶片中的总可溶性蛋白水平低于对照。利用cDNA-AFLP技术,我们从叶片和根系中分别获得了70个和71个差异表达基因。这些基因主要在信号转导、应激反应、碳水化合物和能量代谢、细胞转运、细胞壁和细胞骨架代谢、核酸及蛋白质代谢中发挥作用。脂质代谢(Ca(2+)信号)相关的缺镁响应基因仅从根系(叶片)中分离得到。虽然两者之间缺镁响应基因的数量差异不大,但这些基因大多仅存在于缺镁的叶片或根系中,两者仅共有4个基因。我们的数据清楚地表明,缺镁诱导的生理和基因表达变化在叶片和根系之间存在很大差异。此外,我们重点讨论了缺镁叶片光合下降的原因以及根系对缺镁的响应。