Institute of Plant Nutritional Physiology and Molecular Biology, College of Resources and Environment, Fujian Agriculture and Forestry University (FAFU), 15 Shangxiadian Road, Cangshan District, Fuzhou 350002, China.
Guangxi Key Laboratory of Citrus Biology, Guangxi Academy of Specialty Crops, 40 Putuo Road, Qixing District, Guilin 541004, China.
Tree Physiol. 2020 Aug 29;40(9):1277-1291. doi: 10.1093/treephys/tpaa059.
Little is known about the physiological and molecular mechanisms underlying magnesium (Mg)-deficiency-induced enlargement, cracking and lignification of midribs and main lateral veins of Citrus leaves. Citrus sinensis (L.) Osbeck seedlings were irrigated with nutrient solution at a concentration of 0 (Mg-deficiency) or 2 (Mg-sufficiency) mM Mg(NO3)2 for 16 weeks. Enlargement, cracking and lignification of veins occurred only in lower leaves, but not in upper leaves. Total soluble sugars (glucose + fructose + sucrose), starch and cellulose concentrations were less in Mg-deficiency veins of lower leaves (MDVLL) than those in Mg-sufficiency veins of lower leaves (MSVLL), but lignin concentration was higher in MDVLL than that in MSVLL. However, all four parameters were similar between Mg-deficiency veins of upper leaves (MDVUL) and Mg-sufficiency veins of upper leaves (MSVUL). Using label-free, liquid chromatography-tandem mass spectrometry (LC-MS/MS) analysis, we identified 1229 and 492 differentially abundant proteins (DAPs) in MDVLL vs MSVLL and MDVUL vs MSVUL, respectively. Magnesium-deficiency-induced alterations of Mg, nonstructural carbohydrates, cell wall components, and protein profiles were greater in veins of lower leaves than those in veins of upper leaves. The increased concentration of lignin in MDVLL vs MSVLL might be caused by the following factors: (i) repression of cellulose and starch accumulation promoted lignin biosynthesis; (ii) abundances of proteins involved in phenylpropanoid biosynthesis pathway, hormone biosynthesis and glutathione metabolism were increased; and (iii) the abundances of the other DAPs [viz., copper/zinc-superoxide dismutase, ascorbate oxidase (AO) and ABC transporters] involved in lignin biosynthesis were elevated. Also, the abundances of several proteins involved in cell wall metabolism (viz., expansins, Rho GTPase-activating protein gacA, AO, monocopper oxidase-like protein and xyloglucan endotransglucosylase/hydrolase) were increased in MDVLL vs MSVLL, which might be responsible for the enlargement and cracking of leaf veins.
关于镁缺乏引起柑橘叶片中脉和主侧脉扩大、开裂和木质化的生理和分子机制知之甚少。用浓度为 0(缺镁)或 2(镁充足)mM 的 Mg(NO3)2 的营养液灌溉甜橙(L.)Osbeck 幼苗 16 周。仅在下叶叶脉中发生扩大、开裂和木质化,而上叶叶脉中则没有。与镁充足下叶叶脉(MSVLL)相比,缺镁下叶叶脉(MDVLL)中的总可溶性糖(葡萄糖+果糖+蔗糖)、淀粉和纤维素浓度较低,但木质素浓度较高。然而,上叶叶脉的 MDVUL 和 MSVUL 之间的所有四个参数都相似。使用无标记、液相色谱-串联质谱(LC-MS/MS)分析,我们分别在 MDVLL 与 MSVLL 和 MDVUL 与 MSVUL 之间鉴定出 1229 种和 492 种差异丰度蛋白(DAP)。与上叶叶脉相比,缺镁下叶叶脉中镁、非结构性碳水化合物、细胞壁成分和蛋白质谱的变化更大。MDVLL 中木质素浓度的增加可能是由以下因素引起的:(i)纤维素和淀粉积累的抑制促进木质素生物合成;(ii)参与苯丙烷生物合成途径、激素生物合成和谷胱甘肽代谢的蛋白质丰度增加;(iii)参与木质素生物合成的其他 DAPs[即铜/锌超氧化物歧化酶、抗坏血酸氧化酶(AO)和 ABC 转运蛋白]的丰度升高。此外,MDVLL 中细胞壁代谢相关蛋白(如扩展蛋白、Rho GTP 酶激活蛋白 gacA、AO、单铜氧化酶样蛋白和木葡聚糖内转糖苷酶/水解酶)的丰度也增加,这可能是叶片叶脉扩大和开裂的原因。