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...
Gespeichert in:
Veröffentlicht in: | Plant science (Limerick) 2015-02, Vol.231, p.131-137 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
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 |