The nitrate/proton antiporter AtCLCa mediates nitrate accumulation in plant vacuoles

被引:372
作者
De Angeli, A.
Monachello, D.
Ephritikhine, G.
Frachisse, J. M.
Thomine, S.
Gambale, F.
Barbier-Brygoo, H.
机构
[1] CNRS, UPR 2355, Inst Sci Vegetal, F-91198 Gif Sur Yvette, France
[2] Univ Paris 07, UFR Biol Sci Nat, F-75251 Paris 05, France
[3] CNR, Ist Biofis, I-16149 Genoa, Italy
关键词
D O I
10.1038/nature05013
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Nitrate, the major nitrogen source for most plants, is widely used as a fertilizer and as a result has become a predominant freshwater pollutant. Plants need nitrate for growth and store most of it in the central vacuole(1). Some members of the chloride channel (CLC) protein family, such as the torpedo-fish ClC-0 and mammalian ClC-1, are anion channels(2,3), whereas the bacterial ClC-ec1 and mammalian ClC-4 and ClC-5 have recently been characterized as Cl-/H+ exchangers with unknown cellular functions(4-6). Plant members of the CLC family are proposed to be anion channels(7,8) involved in nitrate homeostasis(9); however, direct evidence for anion transport mediated by a plant CLC is still lacking. Here we show that Arabidopsis thaliana CLCa (AtCLCa) is localized to an intracellular membrane, the tonoplast of the plant vacuole, which is amenable to electrophysiological studies, and we provide direct evidence for its anion transport ability. We demonstrate that AtCLCa is able to accumulate specifically nitrate in the vacuole and behaves as a NO3-/H+ exchanger. For the first time, to our knowledge, the transport activity of a plant CLC is revealed, the antiporter mechanism of a CLC protein is investigated in a native membrane system, and this property is directly connected with its physiological role.
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页码:939 / 942
页数:4
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