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Filleur, S.

Publications and source records attributed to Filleur, S..

2 recordsLinked to original sources

Overexpressing NRT2.7 induces nitrate export from the vacuole and increases growth of Arabidopsis

Nitrogen nutrition is essential for crop yield but applying fertilizers has detrimental effects on the environment. Compartmenting nitrate into vacuoles is one of the options to develop Nitrogen-efficient crop adapted to less fertilizers. Only few proteins involved in nitrate transport on the tonoplast have been identified. CLCa is the major transporter involved in nitrate storage in Arabidopsis but it can also facilitate nitrate remobilization from the vacuole in guard cells. Several other nitrate transporters amongst NRT2.7 have been localized in this membrane. The transport mechanism of NRT2.7 has not yet been defined as this protein is present mainly in seed cells that are not easily amenable for electrophysiology analysis. Here, we investigated NRT2.7 function through its ectopic overexpression in a clca knock-out mutant. Although the growth diminution of clca on nitrogen sufficient medium was complemented, nitrate homeostasis was not restored by NRT2.7 activity. Moreover, NRT2.7 ectopic overexpression in wild-type background (WT) increased growth under limiting nitrogen supply, suggesting that NRT2.7 stimulates nitrate efflux from vacuoles. This hypothesis was demonstrated by electrophysiological nitrate flux measurements on isolated vacuoles. This discovery of NRT2.7 function and more largely the coupling of vacuolar nitrate fluxes with growth under low nitrate supply, will enable new strategies for engineering better NUE for a more sustainable agriculture. HighlightThe overexpression of the nitrate transporter NRT2.7 stimulates growth by increasing the export of nitrate from the vacuole, the main cell compartment for nitrate storage.

plant biology↗

Proton exchange in the nitrate vacuolar transporter AtCLCa is required for growth and nitrogen use efficiency

Nitrate is a major nutrient and osmoticum for plants. To deal with its fluctuating availability in soils, plants store it into vacuoles. AtCLCa, a 2NO3-/1H+ exchanger localized on the vacuole ensures this storage process. It belongs to the CLC family that includes exchangers and channels. A mutation in a glutamate residue conserved across CLC exchangers is likely responsible for the conversion of exchangers to channels. Here, we show that a clca mutant of this residue, E203, behaves as an anion channel in its native membrane. To investigate its physiological importance, we introduced the AtCLCaE203Apoint mutation in a clca KO mutant. We first showed that these AtCLCaE203A mutants display a growth deficit linked to water homeostasis disruption. Additionally, AtCLCaE203Aexpression is not able to complement the clca defect in nitrate accumulation and favors higher N-assimilation at the vegetative stage. Further analyses at post-flowering stages indicated that AtCLCaE203A results in an increase of N uptake allocation to seeds, leading to a higher nitrogen use efficiency compared to wild-type. Altogether, these results point out the critical function of the AtCLCa exchanger on the vacuole for plant metabolism and development.

plant biology↗