Vacuolar Ca2+/H+ Transport Activity Is Required for Systemic Phosphate Homeostasis Involving Shoot-to-Root Signaling in Arabidopsis

被引:64
|
作者
Liu, Tzu-Yin [1 ]
Aung, Kyaw [1 ,2 ]
Tseng, Ching-Ying [1 ]
Chang, Tzu-Yun [1 ]
Chen, Ying-Shin [1 ]
Chiou, Tzyy-Jen [1 ,2 ,3 ]
机构
[1] Acad Sinica, Agr Biotechnol Res Ctr, Taipei 115, Taiwan
[2] Acad Sinica, Mol & Biol Agr Sci Program, Taiwan Int Grad Program, Taipei 115, Taiwan
[3] Natl Chung Hsing Univ, Dept Life Sci, Taichung 402, Taiwan
关键词
PLASMA-MEMBRANE; V-ATPASE; EXPRESSION; STARVATION; CAX1; MICRORNA399; PHO2; THALIANA; STRESS; MUTANT;
D O I
10.1104/pp.111.175257
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Calcium ions (Ca2+) and Ca2+-related proteins mediate a wide array of downstream processes involved in plant responses to abiotic stresses. In Arabidopsis (Arabidopsis thaliana), disruption of the vacuolar Ca2+/H+ transporters CAX1 and CAX3 causes notable alterations in the shoot ionome, including phosphate (P-i) content. In this study, we showed that the cax1/cax3 double mutant displays an elevated P-i level in shoots as a result of increased P-i uptake in a miR399/PHO2-independent signaling pathway. Microarray analysis of the cax1/cax3 mutant suggests the regulatory function of CAX1 and CAX3 in suppressing the expression of a subset of shoot P-i starvation-responsive genes, including genes encoding the PHT1;4 P-i transporter and two SPX domain-containing proteins, SPX1 and SPX3. Moreover, although the expression of several PHT1 genes and PHT1;1/2/3 proteins is not up-regulated in the root of cax1/cax3, results from reciprocal grafting experiments indicate that the cax1/cax3 scion is responsible for high P-i accumulation in grafted plants and that the pht1;1 rootstock is sufficient to moderately repress such P-i accumulation. Based on these findings, we propose that CAX1 and CAX3 mediate a shoot-derived signal that modulates the activity of the root P-i transporter system, likely in part via posttranslational regulation of PHT1;1 P-i transporters.
引用
收藏
页码:1176 / 1189
页数:14
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