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Broutin, J.

Publications and source records attributed to Broutin, J..

2 recordsLinked to original sources

Defects in the Arabidopsis V-ATPase associated RAVE complex affects endosomal pH and triggers the onset of leaf cell clusters upon TOR inhibition

The TOR kinase is an important and conserved signaling hub in plants, as in other eukaryotes. However, the identification of the TOR pathway components and regulators in plants is still fragmentary. Using a genetic screen based on altered sensitivity to TOR inhibitors, we have selected an Arabidopsis mutant that develops leaf ectopic cell clusters of enlarged cells in a TOR-inhibition dependent manner. We have named this mutant loki (Localized growth depending on TOR Kinase Inhibition) and identified the causal mutation in a gene coding for the Arabidopsis homolog of the yeast Rav1 protein. This protein serves as the scaffold for the RAVE complex (Regulator of the ATPase of Vacuolar and Endosomal membranes), which regulates the V-ATPase activity in yeasts and animals. The overall V-ATPase activity is decreased in loki mutants and consistently the endosomal pH is increased. However, the vacuolar pH was found to be unaffected by this mutation. Interestingly, the det3 mutant, which is affected in the C subunit of the V-ATPase, also develops similar cell clusters. Finally, transcriptomic and metabolic analyses revealed that many pathways are affected by both the loki and det3 mutations, including cell wall integrity. This study establishes a new connection between the V-ATPase and the central TOR kinase in plants.

plant biology↗

The Arabidopsis Target of Rapamycin (TOR) kinase regulates ammonium assimilation and glutamine metabolism

In Eukaryotes, Target of Rapamycin (TOR) is a well conserved kinase that controls cell metabolism and growth in response to nutrients and environmental factors. Nitrogen (N) is an essential element for plants and TOR functions as a crucial N and amino acid sensor in animals and yeast. However, the knowledge on the connections between TOR and the overall N metabolism and assimilation in plants is still limited. In this study, we investigate the regulation of TOR in Arabidopsis by the N source as well as the impact of TOR deficiency on N metabolism. Inhibition of TOR globally decreases ammonium uptake while triggering a massive accumulation of amino acids such as Gln, but also of polyamines. Coherently, TOR complex mutants were found to be hypersensitive to Gln. We also show that the glutamine synthetase inhibitor glufosinate abolishes Gln accumulation resulting from TOR inhibition and improves the growth of TOR complex mutants. These results suggest that a high level of Gln contributes to the reduction in plant growth resulting from TOR inhibition. Glutamine synthetase activity was reduced by TOR inhibition while the enzyme amount increased. In conclusion our findings show that the TOR pathway is intimately connected to N metabolism and that a decrease in TOR activity results in a glutamine synthetase-dependent Gln and amino acids accumulation. One sentence summaryThe conserved Target of Rapamycin (TOR) kinase is an important sensor and regulator of the nitrogen metabolism and here we show that inhibiting this kinase affects ammonium uptake and results in Gln accumulation in a glutamine synthetase-dependent manner.

plant biology↗