Morcuende Rosa, Bari Rajendra, Gibon Yves, Zheng Wenming, Pant Bikram Datt, Bläsing Oliver, Usadel Björn, Czechowski Tomasz, Udvardi Michael K, Stitt Mark, Scheible Wolf-Rüdiger
Max-Planck Institute for Molecular Plant Physiology, Science Park Golm, 14476 Potsdam, Germany.
Plant Cell Environ. 2007 Jan;30(1):85-112. doi: 10.1111/j.1365-3040.2006.01608.x.
Affymetrix ATH1 arrays, large-scale real-time reverse transcription PCR of approximately 2200 transcription factor genes and other gene families, and analyses of metabolites and enzyme activities were used to investigate the response of Arabidopsis to phosphate (Pi) deprivation and re-supply. Transcript data were analysed with MapMan software to identify coordinated, system-wide changes in metabolism and other cellular processes. Phosphorus (P) deprivation led to induction or repression of > 1000 genes involved in many processes. A subset, including the induction of genes involved in P uptake, the mobilization of organic Pi, the conversion of phosphorylated glycolytic intermediates to carbohydrates and organic acids, the replacement of P-containing phospholipids with galactolipids and the repression of genes involved in nucleotide/nucleic acid synthesis, was reversed within 3 h after Pi re-supply. Analyses of 22 enzyme activities revealed that changes in transcript levels often, but not always, led to changes in the activities of the encoded enzymes in P-deprived plants. Analyses of metabolites confirmed that P deprivation leads to a shift towards the accumulation of carbohydrates, organic acids and amino acids, and that Pi re-supply leads to use of the latter. P-deprived plants also showed large changes in the expression of many genes involved in, for example, secondary metabolism and photosynthesis. These changes were not reversed rapidly upon Pi re-supply and were probably secondary in origin. Differentially expressed and highly P-specific putative regulator genes were identified that presumably play central roles in coordinating the complex responses of plants to changes in P nutrition. The specific responses to Pi differ markedly from those found for nitrate, whereas the long-term responses during P and N deprivation share common and non-specific features.
利用Affymetrix ATH1基因芯片、对约2200个转录因子基因和其他基因家族进行大规模实时逆转录PCR以及对代谢产物和酶活性进行分析,来研究拟南芥对磷(Pi)缺乏和重新供应的响应。使用MapMan软件分析转录数据,以识别代谢和其他细胞过程中协调的、全系统范围的变化。磷(P)缺乏导致参与许多过程的1000多个基因的诱导或抑制。其中一部分,包括参与磷吸收、有机磷动员、磷酸化糖酵解中间体向碳水化合物和有机酸转化、用半乳糖脂替代含磷磷脂的基因的诱导以及参与核苷酸/核酸合成的基因的抑制,在重新供应Pi后3小时内得以逆转。对22种酶活性的分析表明,转录水平的变化在缺磷植物中常常(但并非总是)导致编码酶活性的变化。代谢产物分析证实,缺磷会导致向碳水化合物、有机酸和氨基酸积累的转变,而重新供应Pi会导致对后者的利用。缺磷植物在许多参与例如次生代谢和光合作用的基因表达上也表现出很大变化。这些变化在重新供应Pi后不会迅速逆转,可能是次生的。鉴定出了差异表达且高度磷特异性的假定调节基因,推测它们在协调植物对磷营养变化的复杂响应中起核心作用。对Pi的特异性响应与对硝酸盐的响应明显不同,而在P和N缺乏期间的长期响应具有共同的非特异性特征。