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OsSPX1参与水稻磷稳态调控。

Involvement of OsSPX1 in phosphate homeostasis in rice.

作者信息

Wang Chuang, Ying Shan, Huang Hongjie, Li Kuan, Wu Ping, Shou Huixia

机构信息

State Key Laboratory of Plant Physiology and Biochemistry, College of Life Sciences, Zhejiang University, Hangzhou, China.

出版信息

Plant J. 2009 Mar;57(5):895-904. doi: 10.1111/j.1365-313X.2008.03734.x. Epub 2008 Nov 4.

Abstract

Arabidopsis thaliana SPX (SYG/PHO81/XPR1) domain genes have recently been shown to be involved in the phosphate (Pi) signaling pathway. We show here that a rice (Oryza sativa) SPX gene, OsSPX1, is specifically induced by Pi starvation in roots. Suppression of OsSPX1 by RNA interference resulted in severe signs of toxicity caused by the over-accumulation of Pi, similar to that found in OsPHR2 (phosphate starvation response transcription factor 2) overexpressors and pho2 (phosphate-responsive mutant 2). Quantitative RT-PCR showed that expression of OsSPX1 was strongly induced in OsPHR2 overexpression and pho2 mutant plants, indicating that OsSPX1 occurs downstream of OsPHR2 and PHO2. The expression of 10 genes associated with the phosphate-starvation signal pathways was analyzed. Expression of OsPT2 (phosphate transporter 2) and OsPT8 was significantly induced in OsSPX1-RNAi (OsSPX1-Ri) plants, suggesting that over-accumulation of Pi in OsSPX1-Ri plants results from an increase in Pi transport. In contrast, overexpression of OsSPX1 suppressed the induction of expression by Pi starvation of all 10 phosphate starvation-induced genes tested: IPS1 (induced by phosphate starvation 1), IPS2, OsPAP10 (purple acid phosphatase 10), OsSQD2 (sulfoquinovosyldiacylglycerol 2), miR399d and miR399j (microRNA 399), OsPT2, OsPT3, OsPT6 and OsPT8. This suggests that OsSPX1 acts via a negative feedback loop to optimize growth under phosphate-limited conditions.

摘要

拟南芥SPX(SYG/PHO81/XPR1)结构域基因最近被证明参与了磷(Pi)信号通路。我们在此表明,水稻(Oryza sativa)的一个SPX基因OsSPX1在根中受到Pi饥饿的特异性诱导。通过RNA干扰抑制OsSPX1会导致Pi过度积累引起的严重毒性迹象,这与在OsPHR2(磷饥饿响应转录因子2)过表达植株和pho2(磷响应突变体2)中发现的情况相似。定量RT-PCR显示,OsSPX1的表达在OsPHR2过表达植株和pho2突变体植株中被强烈诱导,表明OsSPX1位于OsPHR2和PHO2的下游。分析了10个与磷饥饿信号通路相关基因的表达。OsPT2(磷转运蛋白2)和OsPT8的表达在OsSPX1-RNAi(OsSPX1-Ri)植株中显著诱导,这表明OsSPX1-Ri植株中Pi的过度积累是由于Pi转运增加所致。相反,OsSPX1的过表达抑制了所测试的所有10个磷饥饿诱导基因(IPS1(磷饥饿诱导基因1)、IPS2、OsPAP10(紫色酸性磷酸酶10)、OsSQD2(磺基喹喔啉二酰基甘油2)、miR399d和miR399j(微小RNA 399)、OsPT2、OsPT3、OsPT6和OsPT8)在Pi饥饿时的表达诱导。这表明OsSPX1通过负反馈回路发挥作用,以在磷限制条件下优化生长。

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