Grape ASR Regulates Glucose Transport, Metabolism and Signaling

To decipher the mediator role of the grape Abscisic acid, Stress, Ripening (ASR) protein, VvMSA, in the pathways of glucose signaling through the regulation of its target, the promoter of hexose transporter VvHT1, we overexpressed and repressed in embryogenic and non-embryogenic grapevine cells. The...

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Veröffentlicht in:International journal of molecular sciences 2022-05, Vol.23 (11), p.6194
Hauptverfasser: Parrilla, Jonathan, Medici, Anna, Gaillard, Cécile, Verbeke, Jérémy, Gibon, Yves, Rolin, Dominique, Laloi, Maryse, Finkelstein, Ruth R, Atanassova, Rossitza
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Sprache:eng
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Zusammenfassung:To decipher the mediator role of the grape Abscisic acid, Stress, Ripening (ASR) protein, VvMSA, in the pathways of glucose signaling through the regulation of its target, the promoter of hexose transporter VvHT1, we overexpressed and repressed in embryogenic and non-embryogenic grapevine cells. The embryogenic cells with organized cell proliferation were chosen as an appropriate model for high sensitivity to the glucose signal, due to their very low intracellular glucose content and low glycolysis flux. In contrast, the non-embryogenic cells displaying anarchic cell proliferation, supported by high glycolysis flux and a partial switch to fermentation, appeared particularly sensitive to inhibitors of glucose metabolism. By using different glucose analogs to discriminate between distinct pathways of glucose signal transduction, we revealed VvMSA positioning as a transcriptional regulator of the glucose transporter gene in glycolysis-dependent glucose signaling. The effects of both the overexpression and repression of VvMSA on glucose transport and metabolism via glycolysis were analyzed, and the results demonstrated its role as a mediator in the interplay of glucose metabolism, transport and signaling. The overexpression of VvMSA in the mutant provided evidence for its partial functional complementation by improving glucose absorption activity.
ISSN:1422-0067
1661-6596
1422-0067
DOI:10.3390/ijms23116194