Segonzac Cécile, Boyer Jean-Christophe, Ipotesi Emilie, Szponarski Wojciech, Tillard Pascal, Touraine Brigitte, Sommerer Nicolas, Rossignol Michel, Gibrat Rémy
Biochimie et Physiologie Moléculaire des Plantes, Agro-M/Centre National de la Recherche Scientifique/Institut National de la Recherche Agronomique/Université Montpellier 2, France.
Plant Cell. 2007 Nov;19(11):3760-77. doi: 10.1105/tpc.106.048173. Epub 2007 Nov 9.
Root NO(3)(-) efflux to the outer medium is a component of NO(3)(-) net uptake and can even overcome influx upon various stresses. Its role and molecular basis are unknown. Following a functional biochemical approach, NAXT1 (for NITRATE EXCRETION TRANSPORTER1) was identified by mass spectrometry in the plasma membrane (PM) of Arabidopsis thaliana suspension cells, a localization confirmed using a NAXT1-Green Fluorescent Protein fusion protein. NAXT1 belongs to a subclass of seven NAXT members from the large NITRATE TRANSPORTER1/PEPTIDE TRANSPORTER family and is mainly expressed in the cortex of mature roots. The passive NO(3)(-) transport activity (K(m) = 5 mM) in isolated root PM, electrically coupled to the ATP-dependant H(+)-pumping activity, is inhibited by anti-NAXT antibodies. In standard culture conditions, NO(3)(-) contents were altered in plants expressing NAXT-interfering RNAs but not in naxt1 mutant plants. Upon acid load, unidirectional root NO(3)(-) efflux markedly increased in wild-type plants, leading to a prolonged NO(3)(-) excretion regime concomitant with a decrease in root NO(3)(-) content. In vivo and in vitro mutant phenotypes revealed that this response is mediated by NAXT1, whose expression is upregulated at the posttranscriptional level. Strong medium acidification generated a similar response. In vitro, the passive efflux of NO(3)(-) (but not of Cl(-)) was strongly impaired in naxt1 mutant PM. This identification of NO(3)(-) efflux transporters at the PM of plant cells opens the way to molecular studies of the physiological role of NO(3)(-) efflux in stressed or unstressed plants.
根向外部介质的硝酸根外流是硝酸根净吸收的一个组成部分,甚至在各种胁迫下能超过内流。其作用和分子基础尚不清楚。采用功能生化方法,通过质谱在拟南芥悬浮细胞的质膜(PM)中鉴定出了NAXT1(硝酸盐排泄转运体1),利用NAXT1-绿色荧光蛋白融合蛋白证实了其定位。NAXT1属于大的硝酸盐转运体1/肽转运体家族中七个NAXT成员的一个亚类,主要在成熟根的皮层中表达。分离的根质膜中的被动硝酸根转运活性(Km = 5 mM)与依赖ATP的氢离子泵活性电偶联,被抗NAXT抗体抑制。在标准培养条件下,表达NAXT干扰RNA的植物中硝酸根含量发生改变,但在naxt1突变体植物中未改变。在酸负荷下,野生型植物中根的单向硝酸根外流显著增加,导致硝酸根排泄期延长,同时根中硝酸根含量降低。体内和体外突变体表型表明,这种反应由NAXT1介导,其表达在转录后水平上调。强烈的介质酸化产生了类似的反应。在体外,naxt1突变体质膜中硝酸根(而非氯离子)的被动外流严重受损。植物细胞质膜上硝酸根外流转运体的鉴定为研究硝酸根外流在胁迫或非胁迫植物中的生理作用开辟了分子研究途径。