Angkawijaya Artik Elisa, Ngo Anh H, Nguyen Van C, Gunawan Farrel, Nakamura Yuki
Institute of Plant and Microbial Biology, Academia Sinica, Taipei, Taiwan.
Molecular and Biological Agricultural Sciences Program, Taiwan International Graduate Program, Taipei, Taiwan.
Front Plant Sci. 2019 May 29;10:662. doi: 10.3389/fpls.2019.00662. eCollection 2019.
Phosphorus is essential for plant viability. Phosphate-starved plants trigger membrane lipid remodeling to replace membrane phospholipids by non-phosphorus galactolipids presumably to acquire scarce phosphate source. Phosphoethanolamine/phosphocholine phosphatase 1 (PECP1) and phosphate starvation-induced gene 2 (PS2) belong to an emerging class of phosphatase induced by phosphate starvation and dephosphorylates phosphocholine and phosphoethanolamine (PEtn) . However, detailed spatiotemporal expression pattern as well as subcellular localization has not been investigated yet. Here, by constructing transgenic plants harboring functional translational promoter-reporter fusion system, we showed the expression pattern of PECP1 and PS2 in different tissues and in response to phosphate starvation. Besides, the Venus fluorescent reporter revealed that both are localized at the ER. Characterization of transgenic plants that overexpress PECP1 or PS2 showed that their activity toward PEtn may be different . We suggest that PECP1 and PS2 are ER-localized phosphatases that show similar expression pattern yet have a distinct substrate specificity
磷对于植物的生存至关重要。缺磷植物会触发膜脂重塑,用非磷半乳糖脂取代膜磷脂,推测是为了获取稀缺的磷源。磷酸乙醇胺/磷酸胆碱磷酸酶1(PECP1)和磷饥饿诱导基因2(PS2)属于一类由磷饥饿诱导产生的磷酸酶,可使磷酸胆碱和磷酸乙醇胺(PEtn)去磷酸化。然而,其详细的时空表达模式以及亚细胞定位尚未得到研究。在此,通过构建携带功能性翻译启动子-报告基因融合系统的转基因植物,我们展示了PECP1和PS2在不同组织中的表达模式以及对磷饥饿的响应。此外,金星荧光报告基因显示二者均定位于内质网。对过表达PECP1或PS2的转基因植物的表征表明,它们对PEtn的活性可能不同。我们认为,PECP1和PS2是定位于内质网的磷酸酶,它们具有相似的表达模式,但底物特异性不同。