Phang Tsui-Hung, Shao Guihua, Liao Hong, Yan Xiaolong, Lam Hon-Ming
Department of Biology and State (China) Key Laboratory of Agrobiotechnology, The Chinese University of Hong Kong, Hong Kong, China.
Physiol Plant. 2009 Apr;135(4):412-25. doi: 10.1111/j.1399-3054.2008.01200.x. Epub 2009 Feb 5.
Previous studies on the interaction between environmental inorganic phosphate (Pi) and salinity stress using soybean cultivars sensitive to high external Pi had two limitations: (1) the phenotype was dominated by overaccumulation of phosphorus (P); and (2) no detailed analysis was performed for sodium ion uptake. In this study, we focused on the effects of high external Pi on the sodium ion uptake in 'Pi-tolerant' soybean cultivars. The P accumulation in Pi-tolerant soybean Union was much lower [9.0 mg g(-)(1) dry weight (DW); contrasting to 38-76 mg g(-)(1) DW in the 'Pi-sensitive' soybean cultivars]. At in planta level, high level of external Pi significantly (P < 0.001) increased net sodium ion uptake and aggravated salinity stress symptoms. The effects of high external Pi diminished when de-rooted plants were used, suggesting that root is the primary organ interacting with Pi in the growth medium. Two-cell models, including soybean suspension cells and the tobacco Bright Yellow-2 cell line, were also employed to study the effects of high external Pi at the cellular level. Consistent to in planta results, high external Pi uplifted cellular sodium ion uptake and reduced cell viability under salinity stress. Gene expression analyses further showed that HPi (2 mM Pi supplements; excessive level of Pi) could reduce the fold of induction of GmSOS1 and GmCNGC under salinity stress, suggesting that they may be possible molecular targets involved in the interaction between high external Pi and Na(+) uptake.
先前使用对高外源无机磷(Pi)敏感的大豆品种进行的关于环境无机磷与盐胁迫相互作用的研究存在两个局限性:(1)表型主要由磷(P)的过度积累主导;(2)未对钠离子吸收进行详细分析。在本研究中,我们聚焦于高外源Pi对‘耐Pi’大豆品种中钠离子吸收的影响。耐Pi大豆品种Union中的磷积累量要低得多[9.0毫克/克干重(DW);与之形成对比的是,‘对Pi敏感’大豆品种中的磷积累量为38 - 76毫克/克干重]。在植株水平上,高浓度的外源Pi显著(P < 0.001)增加了净钠离子吸收,并加重了盐胁迫症状。当使用去根植株时,高外源Pi的影响减弱,这表明根是与生长培养基中的Pi相互作用的主要器官。还采用了双细胞模型,包括大豆悬浮细胞和烟草Bright Yellow - 2细胞系,来研究高外源Pi在细胞水平上的影响。与植株水平的结果一致,高外源Pi在盐胁迫下提高了细胞的钠离子吸收并降低了细胞活力。基因表达分析进一步表明,高Pi(补充2 mM Pi;过量的Pi水平)可降低盐胁迫下GmSOS1和GmCNGC的诱导倍数,这表明它们可能是参与高外源Pi与Na⁺吸收相互作用的潜在分子靶点。