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Peptidyl-prolyl cis-trans isomerase ROF2 modulates intracellular pH homeostasis in Arabidopsis

Authors :
Ministerio de Ciencia e Innovación (España)
Generalitat Valenciana
Bissoli, Gaetano
Niñoles, Regina
Fresquet, Sandra
Palombieri, Samuela
Bueso, Eduardo
Rubio, Lourdes
García-Sánchez, María J.
Fernández, José A.
Mulet-Salort, José Miguel
Serrano, Ramón
Ministerio de Ciencia e Innovación (España)
Generalitat Valenciana
Bissoli, Gaetano
Niñoles, Regina
Fresquet, Sandra
Palombieri, Samuela
Bueso, Eduardo
Rubio, Lourdes
García-Sánchez, María J.
Fernández, José A.
Mulet-Salort, José Miguel
Serrano, Ramón
Publication Year :
2012

Abstract

Intracellular pH must be kept close to neutrality to be compatible with cellular functions, but the mechanisms of pH homeostasis and the responses to intracellular acidification are mostly unknown. In the plant Arabidopsis thaliana, we found that intracellular acid stress generated by weak organic acids at normal external pH induces expression of several chaperone genes, including ROF2, which encodes a peptidyl-prolyl cis-trans isomerase of the FK506-binding protein class. Loss of function of ROF2, and especially double mutation of ROF2 and the closely related gene ROF1, results in acid sensitivity. Over-expression of ROF2 confers tolerance to intracellular acidification by increasing proton extrusion from cells. The activation of the plasma membrane proton pump (H+-ATPase) is indirect: over-expression of ROF2 activates K+ uptake, causing depolarization of the plasma membrane, which activates the electrogenic H+ pump. The depolarization of ROF2 over-expressing plants explains their tolerance to toxic cations such as lithium, norspermidine and hygromycin B, whose uptake is driven by the membrane potential. As ROF2 induction and intracellular acidification are common consequences of many stresses, this mechanism of pH homeostasis may be of general importance for stress tolerance.

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1104767147
Document Type :
Electronic Resource