RESUMO
The salt overly sensitive (SOS) pathway is the only mechanism known for Na+ extrusion in plant cells. SOS pathway activation involves Ca2+-sensing proteins, such as calcineurin B-like (CBL) proteins, and CBL-interacting protein kinases (CIPKs). In this signalling mechanism, a transit increase in cytosolic Ca2+ concentration triggered by Na+ accumulation is perceived by CBL (also known as SOS3). Afterward, SOS3 physically interacts with a CIPK (also known as SOS2), forming the SOS2/SOS3 complex, which can regulate the number downstream targets, controlling ionic homeostasis. For instance, the SOS2/SOS3 complex phosphorylates and activates the SOS1 plasmalemma protein, which is a Na+/H+ antiporter that extrudes Na+ out of the cell. The CBL-CIPK networking system displays specificity, complexity and diversity, constituting a critical response against salt stress and other abiotic stresses. In a study reported in the journal Plant and Cell Physiology, we showed that NH4+ induces the robust activation of transporters for Na+ homeostasis in root cells, especially the SOS1 antiporter and plasma membrane H+-ATPase, differently than does NO3-. Despite some studies having shown that external NH4+ ameliorates salt-induced effects on ionic homeostasis, there is no evidence that NH4+ per se or some product of its assimilation is responsible for these responses. Here, we speculate about the signalling role behind glutamine in CBL-CIPK modulation, which could effectively activate the SOS pathway in NH4+-fed stressed plants.
