ABSTRACT
The two-pore cation channel TPC1 operates as a dimeric channel in animal and plant endomembranes. Each subunit consists of two homologous Shaker-like halves, with 12 transmembrane domains in total (S1-S6, S7-S12). In plants, TPC1 channels reside in the vacuolar membrane, and upon voltage stimulation, give rise to the well-known slow-activating SV currents. Here, we combined bioinformatics, structure modelling, site-directed mutagenesis, and in planta patch clamp studies to elucidate the molecular mechanisms of voltage-dependent channel gating in TPC1 in its native plant background. Structure-function analysis of the Arabidopsis TPC1 channel in planta confirmed that helix S10 operates as the major voltage-sensing site, with Glu450 and Glu478 identified as possible ion-pair partners for voltage-sensing Arg537. The contribution of helix S4 to voltage sensing was found to be negligible. Several conserved negative residues on the luminal site contribute to calcium binding, stabilizing the closed channel. During evolution of plant TPC1s from two separate Shaker-like domains, the voltage-sensing function in the N-terminal Shaker-unit (S1-S4) vanished.
Subject(s)
Arabidopsis Proteins/metabolism , Arabidopsis/physiology , Calcium Channels/metabolism , Cations/metabolism , Models, Structural , Amino Acid Motifs , Amino Acid Sequence , Arabidopsis/genetics , Arabidopsis Proteins/chemistry , Arabidopsis Proteins/genetics , Biological Evolution , Calcium/metabolism , Calcium Channels/chemistry , Calcium Channels/genetics , Intracellular Membranes/metabolism , Ion Channel Gating , Ion Transport , Models, Molecular , Mutagenesis, Site-Directed , Mutation , Patch-Clamp Techniques , Phylogeny , Protein Domains , Vacuoles/metabolismABSTRACT
A plant's ability to maintain an optimal cytosolic K(+)/Na(+) ratio has long been cited as a key feature of salinity tolerance. As traditional whole-leaf nutrient analysis does not account for tissue and organelle-specific ion sequestration, the predictive value of this index at the whole-plant level is not always satisfactory. Consequently, suitable in situ methods for functionally assessing the activity of the key membrane transporters contributing to this trait at the cellular level need to be developed. The aim of this work was to investigate the extent to which plasma membrane transporter-mediated Na(+) exclusion and KOR-mediated K(+) retention traits, measured with the microelectrode ion flux measuring (MIFE) technique, are inheritable in wheat, and whether the MIFE technique has the potential to be used in combination with molecular markers to determine QTLs for these transporter proteins. Experiments involved two bread (Triticum aestivum) and two durum (Triticum turgidum) wheat lines contrasting in their salinity tolerance. Net Na(+), K(+) and H(+) fluxes were measured from 6-day-old roots of parental lines and their F(1) hybrids upon addition and removal of NaCl. These results were complemented by assessment of whole-plant physiological and agronomic characteristics. We show evidence for a strong heritability of plasma membrane transporter-mediated Na(+) exclusion and K(+) retention traits in wheat at the cellular level. This opens the prospect of using the MIFE technique to map the position of these transporters on particular loci of wheat chromosomes. The next obvious step would be to pyramid these traits in one ideotype with superior salinity tolerance.
