Li Lin, Ye Lingxiao, Kong Qihui, Shou Huixia
State Key Laboratory of Plant Physiology and Biochemistry, College of Life Sciences, Zhejiang University, Hangzhou, China.
The Zhejiang University Affiliated 15st Middle School in Hangzhou, Hangzhou, China.
Front Plant Sci. 2019 Jun 4;10:700. doi: 10.3389/fpls.2019.00700. eCollection 2019.
Ferric reductase oxidase (), the enzyme that reduced ferric iron [Fe (III)] into ferrous iron [Fe (II)], is known to play important roles in Fe absorption and homeostasis in plants that utilize a strategy I mechanism to obtain iron. Rice can use both strategies I and II for Fe uptake depending on the growth conditions. FRO is encoded by two genes in rice genome. Amino acid sequence alignment shows that Os contains all necessary predicted motifs for a functional FRO enzyme, whereas Os lacks a complete transmembrane domain at the N-terminal. Transient expression of OsFRO1: GFP protein fusion revealed that OsFRO1 is localized to the vacuolar membrane in rice protoplast. Os is primarily expressed in leaves and transcript abundance was decreased under excess Fe conditions. Transgenic plants overexpressing Os were more sensitive to Fe toxicity, in contrast RNA interference lines showed more tolerance to Fe excess stress. Furthermore, RNAi lines showed decreased Fe concentrations compared to wild type plants under Fe excess condition. Together these data show that OsFRO1 is involved in reducing ferric Fe into ferrous Fe in the vacuole, and makes the vacuolar stored Fe available to the cytoplasm through Fe (II) or chelated Fe (II) transporters. Under Fe excess condition, the downregulation of in the RNAi plants reduced the amount of Fe (II) available for cytoplasm, to alleviate Fe excess toxicity. This indicates that OsFRO1 plays an important role to maintain Fe homeostasis between the cytoplasm and vacuole in rice.
铁还原氧化酶(),即一种将三价铁[Fe(III)]还原为二价铁[Fe(II)]的酶,已知其在采用策略I机制获取铁的植物的铁吸收和体内平衡中发挥重要作用。水稻可根据生长条件同时使用策略I和策略II来吸收铁。水稻基因组中的两个基因编码铁还原氧化酶。氨基酸序列比对显示,Os含有功能性铁还原氧化酶所有必要的预测基序,而Os在N端缺乏完整的跨膜结构域。OsFRO1:GFP蛋白融合体的瞬时表达表明,OsFRO1定位于水稻原生质体的液泡膜上。Os主要在叶片中表达,在铁过量条件下转录本丰度降低。与野生型植物相比,过表达Os的转基因植物对铁毒性更敏感,相反,RNA干扰株系对铁过量胁迫表现出更强的耐受性。此外,在铁过量条件下,RNA干扰株系的铁浓度与野生型植物相比有所降低。这些数据共同表明,OsFRO1参与将液泡中的三价铁还原为二价铁,并通过二价铁或螯合二价铁转运蛋白使液泡中储存的铁可用于细胞质。在铁过量条件下,RNA干扰植物中OsFRO1的下调减少了可用于细胞质的二价铁量,从而减轻铁过量毒性。这表明OsFRO1在维持水稻细胞质和液泡之间的铁稳态方面发挥着重要作用。