Potassium transporter TRH1 subunits assemble regulating root-hair elongation autonomously from the cell fate determination pathway

•TRH1 acts autonomously modulating root-hair elongation through auxin distribution.•Molecular modeling reveals two highly variable regions between K+ transporters.•Physical interactions identified between these two intracytoplasmic regions of TRH1.•These regions most likely control selective co-asse...

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Veröffentlicht in:Plant science (Limerick) 2015-02, Vol.231, p.131-137
Hauptverfasser: Daras, Gerasimos, Rigas, Stamatis, Tsitsekian, Dikran, Iacovides, Tefkros A., Hatzopoulos, Polydefkis
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Sprache:eng
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Zusammenfassung:•TRH1 acts autonomously modulating root-hair elongation through auxin distribution.•Molecular modeling reveals two highly variable regions between K+ transporters.•Physical interactions identified between these two intracytoplasmic regions of TRH1.•These regions most likely control selective co-assembly of KUP/HAK/KT subunits. Trichoblasts of trh1 plants form root-hair initiation sites that fail to undergo tip growth resulting in a tiny root-hair phenotype. TRH1 belongs to Arabidopsis KT/KUP/HAK potassium transporter family controlling root-hair growth and gravitropism. Double mutant combinations between trh1 and root-hair mutants affecting cell fate or root-hair initiation exhibited additive phenotypes, suggesting that TRH1 acts independently and developmentally downstream of root-hair initiation. Bimolecular Fluorescence Complementation (BiFC), upon TRH1-YFPC and TRH1-YFPN co-transformation into tobacco epidermal cells, led to fluorescence emission indicative of TRH1 subunit homodimerization. Yeast two-hybrid analysis revealed two types of interactions. The hydrophilic segment between the second and the third transmembrane domain extending from residues Q105 to T141 is competent for a relatively weak interaction, whereas the region at the C-terminal beyond the last transmembrane domain, extending from amino acids R565 to A729, strongly self-interacts. These domains likely facilitate the co-assembly of TRH1 subunits forming an active K+ transport system within cellular membrane structures. The results support the role of TRH1 acting as a convergence point between the developmental root-hair pathway and the environmental/hormonal signaling pathway to preserve auxin homeostasis ensuring plant adaptation in changing environments.
ISSN:0168-9452
1873-2259
DOI:10.1016/j.plantsci.2014.11.017