A dominant-negative form of Arabidopsis AP-3 #-adaptin improves intracellular pH homeostasis
Fecha
Autores
Rubio, Lourdes
García Sánchez, María J.
Fernandez, Jose A.
Alejandro Martínez, Santiago
Directores
Handle
https://riunet.upv.es/handle/10251/68694
Cita bibliográfica
Niñoles Rodenes, R.; Rubio, L.; García Sánchez, MJ.; Fernandez, JA.; Bueso Ródenas, E.; Alejandro Martínez, S.; Serrano Salom, R. (2013). A dominant-negative form of Arabidopsis AP-3 #-adaptin improves intracellular pH homeostasis. Plant Journal. 74(4):557-568. https://doi.org/10.1111/tpj.12138
Titulación
Resumen
[EN] Intracellular pH (pHi) is a crucial parameter in cellular physiology but its mechanisms of homeostasis are only partially understood. To uncover novel roles and participants of the pHi regulatory system, we have screened an Arabidopsis mutant collection for resistance of seed germination to intracellular acidification induced by weak organic acids (acetic, propionic, sorbic). The phenotypes of one identified mutant, weak acid-tolerant 1-1D (wat1-1D) are due to the expression of a truncated form of AP-3 -adaptin (encoded by the PAT2 gene) that behaves as a as dominant-negative. During acetic acid treatment the root epidermal cells of the mutant maintain a higher pHi and a more depolarized plasma membrane electrical potential than wild-type cells. Additional phenotypes of wat1-1D roots include increased rates of acetate efflux, K+ uptake and H+ efflux, the latter reflecting the in vivo activity of the plasma membrane H+-ATPase. The in vitro activity of the enzyme was not increased but, as the H+-ATPase is electrogenic, the increased ion permeability would allow a higher rate of H+ efflux. The AP-3 adaptor complex is involved in traffic from Golgi to vacuoles but its function in plants is not much known. The phenotypes of the wat1-1D mutant can be explained if loss of function of the AP-3 -adaptin causes activation of channels or transporters for organic anions (acetate) and for K+ at the plasma membrane, perhaps through miss-localization of tonoplast proteins. This suggests a role of this adaptin in trafficking of ion channels or transporters to the tonoplast.
Palabras clave
Arabidopsis thaliana, H plus -ATPase, Membrane potential, Ion channels, Acetic acid
ISSN
0960-7412
ISBN
Fuente
Plant Journal
DOI
10.1111/tpj.12138
Enlaces relacionados
Agradecimientos
This work was supported by grants BFU2008-00604 from the 'Ministerio de Ciencia e Innovacion' (Madrid, Spain) and from PROME-TEO/2010/038 of the 'Conselleria de Educacion' (Valencia, Spain). We thank Frans J. Maathuis (York, United Kingdom) for the pA7-TPK1-GFP plasmid, Enrico Martinoia (Zurich, Switzerland) for the pART7-ALMT9-GFP plasmid and for the tdt mutant, Karin Schumacher (Heidelberg, Germany) for the vha-a2 vha-a3 mutant, Jose M. Pardo (Sevilla, Spain) for the nhx2-1 mutant, NASC for the akt1-1 mutant, Roberto A. Gaxiola (Tempe, Arizona) for the AVP1 over-expression line and Wei-Hua Wu (Beijing, China) for the AKT1 over-expression line. R. Ninoles was supported by a JAE-preDOC contract ('Consejo Superior de Investigaciones Cientificas', Madrid, Spain).