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Métodos Terapéuticos y Terapias MTCI
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1.
Int J Mol Sci ; 22(6)2021 Mar 16.
Artículo en Inglés | MEDLINE | ID: mdl-33809409

RESUMEN

Yellow lupine is a great model for abscission-related research given that excessive flower abortion reduces its yield. It has been previously shown that the EPIP peptide, a fragment of LlIDL (INFLORESCENCE DEFICIENT IN ABSCISSION) amino-acid sequence, is a sufficient molecule to induce flower abortion, however, the question remains: What are the exact changes evoked by this peptide locally in abscission zone (AZ) cells? Therefore, we used EPIP peptide to monitor specific modifications accompanied by early steps of flower abscission directly in the AZ. EPIP stimulates the downstream elements of the pathway-HAESA and MITOGEN-ACTIVATED PROTEIN KINASE6 and induces cellular symptoms indicating AZ activation. The EPIP treatment disrupts redox homeostasis, involving the accumulation of H2O2 and upregulation of the enzymatic antioxidant system including superoxide dismutase, catalase, and ascorbate peroxidase. A weakening of the cell wall structure in response to EPIP is reflected by pectin demethylation, while a changing pattern of fatty acids and acyl lipids composition suggests a modification of lipid metabolism. Notably, the formation of a signaling molecule-phosphatidic acid is induced locally in EPIP-treated AZ. Collectively, all these changes indicate the switching of several metabolic and signaling pathways directly in the AZ in response to EPIP, which inevitably leads to flower abscission.


Asunto(s)
Flores/crecimiento & desarrollo , Homeostasis , Lípidos/química , Lupinus/crecimiento & desarrollo , Pectinas/metabolismo , Péptidos/farmacología , Pared Celular/efectos de los fármacos , Pared Celular/metabolismo , Flores/efectos de los fármacos , Homeostasis/efectos de los fármacos , Peróxido de Hidrógeno/metabolismo , Lupinus/efectos de los fármacos , Oxidación-Reducción , Proteínas de Plantas/genética , Proteínas de Plantas/metabolismo , Transducción de Señal/efectos de los fármacos , Superóxido Dismutasa/metabolismo
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