Martin Luther University Halle-Wittenberg, Biocenter, Weinbergweg, Halle (Saale), Germany.
Institute of Plant Biochemistry, Department of Cell and Metabolic Biology, Weinberg, Halle (Saale), Germany.
J Exp Bot. 2018 Jan 23;69(3):467-481. doi: 10.1093/jxb/erx408.
A universal plant response to phosphorus deprivation is the up-regulation of a diverse array of phosphatases. As reported recently, the AtPECP1 gene encodes a phosphatase with in vitro substrate specificity for phosphoethanolamine and phosphocholine. The putative substrates suggested that AtPECP1 is related to phospholipid metabolism; however, the biological function of AtPECP1 is as yet not understood. In addition, whereas lipid remodelling processes as part of the phosphorus starvation response have been extensively studied, knowledge of the polar head group metabolism and its regulation is lacking. We found that AtPECP1 is expressed in the cytosol and exerts by far its strongest activity in roots of phosphate-starved plants. We established a novel LC-MS/MS-based method for the quantitative and simultaneous measurement of the head group metabolites. The analysis of Atpecp1 null mutants and overexpression lines revealed that phosphoethanolamine, but not phosphocholine is the substrate of AtPECP1 in vivo. The impact on head group metabolite levels is greatest in roots of both loss-of-function and gain-of-function transgenic lines, indicating that the biological role of AtPECP1 is mainly restricted to roots. We suggest that phosphoethanolamine hydrolysis by AtPECP1 during Pi starvation is required to down-regulate the energy-consuming biosynthesis of phosphocholine through the methylation pathway.
植物对磷饥饿的普遍反应是上调多种磷酸酶。最近有报道称,AtPECP1 基因编码一种具有体外对磷酸乙醇胺和磷酸胆碱底物特异性的磷酸酶。推测的底物表明 AtPECP1 与磷脂代谢有关;然而,AtPECP1 的生物学功能尚不清楚。此外,尽管作为磷饥饿反应一部分的脂类重塑过程已经得到了广泛的研究,但对极性头部基团代谢及其调控的了解还很缺乏。我们发现 AtPECP1 在细胞质中表达,并在缺磷植物的根中表现出最强的活性。我们建立了一种新的基于 LC-MS/MS 的方法,用于定量和同时测量头部基团代谢物。对 Atpecp1 缺失突变体和过表达系的分析表明,磷酸乙醇胺而不是磷酸胆碱是 AtPECP1 在体内的底物。在失活和功能获得转基因系的根中,头部基团代谢物水平的变化最大,这表明 AtPECP1 的生物学作用主要局限于根。我们认为,在 Pi 饥饿期间,AtPECP1 水解磷酸乙醇胺是通过甲基化途径下调磷酸胆碱这种耗能生物合成所必需的。