Boursiac Yann, Chen Sheng, Luu Doan-Trung, Sorieul Mathias, van den Dries Niels, Maurel Christophe
Biochimie et Physiologie Moléculaire des Plantes, Agro-Montpellier/Centre National de la Recherche Scientifique/Institut National de la Recheche Agonomique/Université Montpellier 2, Unité Mixte de Recherche 5004, France.
Plant Physiol. 2005 Oct;139(2):790-805. doi: 10.1104/pp.105.065029. Epub 2005 Sep 23.
Aquaporins facilitate the uptake of soil water and mediate the regulation of root hydraulic conductivity (Lp(r)) in response to a large variety of environmental stresses. Here, we use Arabidopsis (Arabidopsis thaliana) plants to dissect the effects of salt on both Lp(r) and aquaporin expression and investigate possible molecular and cellular mechanisms of aquaporin regulation in plant roots under stress. Treatment of plants by 100 mm NaCl was perceived as an osmotic stimulus and induced a rapid (half-time, 45 min) and significant (70%) decrease in Lp(r), which was maintained for at least 24 h. Macroarray experiments with gene-specific tags were performed to investigate the expression of all 35 genes of the Arabidopsis aquaporin family. Transcripts from 20 individual aquaporin genes, most of which encoded members of the plasma membrane intrinsic protein (PIP) and tonoplast intrinsic protein (TIP) subfamilies, were detected in nontreated roots. All PIP and TIP aquaporin transcripts with a strong expression signal showed a 60% to 75% decrease in their abundance between 2 and 4 h following exposure to salt. The use of antipeptide antibodies that cross-reacted with isoforms of specific aquaporin subclasses revealed that the abundance of PIP1s decreased by 40% as early as 30 min after salt exposure, whereas PIP2 and TIP1 homologs showed a 20% to 40% decrease in abundance after 6 h of treatment. Expression in transgenic plants of aquaporins fused to the green fluorescent protein revealed that the subcellular localization of TIP2;1 and PIP1 and PIP2 homologs was unchanged after 45 min of exposure to salt, whereas a TIP1;1-green fluorescent protein fusion was relocalized into intracellular spherical structures tentatively identified as intravacuolar invaginations. The appearance of intracellular structures containing PIP1 and PIP2 homologs was occasionally observed after 2 h of salt treatment. In conclusion, this work shows that exposure of roots to salt induces changes in aquaporin expression at multiple levels. These changes include a coordinated transcriptional down-regulation and subcellular relocalization of both PIPs and TIPs. These mechanisms may act in concert to regulate root water transport, mostly in the long term (> or =6 h).
水通道蛋白促进土壤水分的吸收,并介导根系水力导度(Lp(r))对多种环境胁迫的响应调节。在此,我们利用拟南芥植株剖析盐分对Lp(r)和水通道蛋白表达的影响,并研究胁迫条件下植物根中水通道蛋白调节的可能分子和细胞机制。用100 mM NaCl处理植株被视为一种渗透刺激,可诱导Lp(r)迅速(半衰期为45分钟)且显著(70%)下降,并至少维持24小时。利用基因特异性标签进行宏阵列实验,以研究拟南芥水通道蛋白家族所有35个基因的表达。在未处理的根中检测到来自20个单个水通道蛋白基因的转录本,其中大多数编码质膜内在蛋白(PIP)和液泡膜内在蛋白(TIP)亚家族的成员。所有具有强表达信号的PIP和TIP水通道蛋白转录本在盐处理后2至4小时内其丰度下降了60%至75%。使用与特定水通道蛋白亚类同工型发生交叉反应的抗肽抗体显示,盐处理后30分钟内PIP1s的丰度就下降了40%,而PIP2和TIP1同源物在处理6小时后丰度下降了20%至40%。水通道蛋白与绿色荧光蛋白融合在转基因植物中的表达显示,盐处理45分钟后TIP2;1以及PIP1和PIP2同源物的亚细胞定位未发生变化,而TIP1;1 - 绿色荧光蛋白融合体重新定位到暂定为液泡内陷的细胞内球形结构中。盐处理2小时后偶尔会观察到含有PIP1和PIP2同源物的细胞内结构的出现。总之,这项工作表明根系暴露于盐中会在多个水平上诱导水通道蛋白表达的变化。这些变化包括PIPs和TIPs的协同转录下调和亚细胞重新定位。这些机制可能共同作用来调节根系水分运输,主要是在长期(≥6小时)。