Hyperacidification of Vacuoles by the Combined Action of Two Different P-ATPases in the Tonoplast Determines Flower Color

被引:126
作者
Faraco, Marianna [1 ]
Spelt, Cornelis [1 ]
Bliek, Mattijs [1 ]
Verweij, Walter [1 ]
Hoshino, Atsushi [1 ,2 ,3 ]
Espen, Luca [4 ]
Prinsi, Bhakti [4 ]
Jaarsma, Rinse [1 ]
Tarhan, Eray [1 ]
de Boer, Albertus H. [1 ]
Di Sansebastiano, Gian-Pietro [5 ]
Koes, Ronald [1 ]
Quattrocchio, Francesca M. [1 ]
机构
[1] Vrije Univ Amsterdam, Grad Sch Expt Plant Sci, Dept Mol Cell Biol, NL-1081 HV Amsterdam, Netherlands
[2] Natl Inst Basic Biol, Okazaki, Aichi, Japan
[3] Grad Univ Adv Studies Sokendai, Dept Basic Biol, Okazaki, Aichi 4448585, Japan
[4] Univ Milan, Dipartimento Sci Agr & Ambientali, I-20133 Milan, Italy
[5] Univ Salento, Di S Te B A, I-73100 Lecce, Italy
来源
CELL REPORTS | 2014年 / 6卷 / 01期
关键词
MEMBRANE H+-ATPASE; PROTEIN; PETUNIA; GENES; PHOSPHORYLATION; TRANSCRIPTION; ENERGIZATION; TRANSPORT; MECHANISM; BINDING;
D O I
10.1016/j.celrep.2013.12.009
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The acidification of endomembrane compartments is essential for enzyme activities, sorting, trafficking, and trans-membrane transport of various compounds. Vacuoles are mildly acidic inmost plant cells because of the action of V-ATPase and/or pyrophosphatase proton pumps but are hyperacidified in specific cells by mechanisms that remained unclear. Here, we show that the blue petal color of petunia ph mutants is due to a failure to hyperacidify vacuoles. We report that PH1 encodes a P-3B-ATPase, hitherto known as Mg2+ transporters in bacteria only, that resides in the vacuolar membrane (tonoplast). In vivo nuclear magnetic resonance and genetic data show that PH1 is required and, together with the tonoplast H+ P-3A-ATPase PH5, sufficient to hyperacidify vacuoles. PH1 has no H+ transport activity on its own but can physically interact with PH5 and boost PH5 H+ transport activity. Hence, the hyperacidification of vacuoles in petals, and possibly other tissues, relies on a heteromeric P-ATPase pump.
引用
收藏
页码:32 / 43
页数:12
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