Armengaud Patrick, De Angeli Alexis, Berquin Patrick, Bréhaut Virginie, Durand Mickaël, Daniel-Vedele Françoise, Krapp Anne, Filleur Sophie
Université Paris-Saclay, INRAE, AgroParisTech, Institut Jean-Pierre Bourgin for Plant Sciences (IJPB), 78000, Versailles, France.
Université Paris-Saclay, CEA, CNRS, Institute for Integrative Biology of the Cell (I2BC), 91198, Gif-sur-Yvette, France.
J Exp Bot. 2025 Jun 26. doi: 10.1093/jxb/eraf288.
Nitrogen nutrition is essential for crop yield but applying fertilizers has detrimental effects on the environment. Compartmenting nitrate into vacuoles is one of the options to develop Nitrogen-efficient crop adapted to less fertilizers. Only few proteins involved in nitrate transport on the tonoplast have been identified. CLCa is the major transporter involved in nitrate storage in Arabidopsis but it can also facilitate nitrate remobilization from the vacuole in guard cells. Several other nitrate transporters amongst NRT2.7 have been localized in this membrane. The transport mechanism of NRT2.7 has not yet been defined as this protein is present mainly in seed cells that are not easily amenable for electrophysiology analysis. Here, we investigated NRT2.7 function through its ectopic overexpression in a clca knock-out mutant. Although the growth diminution of clca on nitrogen sufficient medium was complemented, nitrate homeostasis was not restored by NRT2.7 activity. Moreover, NRT2.7 ectopic overexpression in wild-type background (WT) increased growth under limiting nitrogen supply, suggesting that NRT2.7 stimulates nitrate efflux from vacuoles. This hypothesis was demonstrated by electrophysiological nitrate flux measurements on isolated vacuoles. This discovery of NRT2.7 function and more largely the coupling of vacuolar nitrate fluxes with growth under low nitrate supply, will enable new strategies for engineering better NUE for a more sustainable agriculture.
氮素营养对作物产量至关重要,但施用化肥会对环境产生不利影响。将硝酸盐分隔到液泡中是培育适应较少化肥的氮高效作物的一种选择。目前仅鉴定出少数参与液泡膜上硝酸盐转运的蛋白质。CLCa是拟南芥中参与硝酸盐储存的主要转运蛋白,但它也能促进保卫细胞液泡中硝酸盐的再动员。NRT2.7中的其他几种硝酸盐转运蛋白也已定位在该膜上。由于NRT2.7主要存在于不易进行电生理分析的种子细胞中,其转运机制尚未明确。在此,我们通过在clca基因敲除突变体中异位过表达来研究NRT2.7的功能。尽管在氮充足培养基上clca突变体的生长减弱现象得到了互补,但NRT2.7的活性并未恢复硝酸盐稳态。此外,在野生型背景(WT)中异位过表达NRT2.7可在有限氮供应条件下促进生长,这表明NRT2.7刺激了液泡中硝酸盐的外流。通过对分离液泡进行电生理硝酸盐通量测量证实了这一假设。NRT2.7功能的这一发现,以及更广泛地说液泡硝酸盐通量与低硝酸盐供应条件下生长的耦合,将为设计更好的氮利用效率以实现更可持续农业提供新策略。