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TMK-based cell-surface auxin signalling activates cell-wall acidification.

Wenwei LinXiang ZhouWenxin TangKoji TakahashiXue PanJiawei DaiHong RenXiaoyue ZhuSongqin PanHaiyan ZhengWilliam M GrayTongda XuToshinori KinoshitaZhenbiao Yang
Published in: Nature (2021)
The phytohormone auxin controls many processes in plants, at least in part through its regulation of cell expansion1. The acid growth hypothesis has been proposed to explain auxin-stimulated cell expansion for five decades, but the mechanism that underlies auxin-induced cell-wall acidification is poorly characterized. Auxin induces the phosphorylation and activation of the plasma membrane H+-ATPase that pumps protons into the apoplast2, yet how auxin activates its phosphorylation remains unclear. Here we show that the transmembrane kinase (TMK) auxin-signalling proteins interact with plasma membrane H+-ATPases, inducing their phosphorylation, and thereby promoting cell-wall acidification and hypocotyl cell elongation in Arabidopsis. Auxin induced interactions between TMKs and H+-ATPases in the plasma membrane within seconds, as well as TMK-dependent phosphorylation of the penultimate threonine residue on the H+-ATPases. Our genetic, biochemical and molecular evidence demonstrates that TMKs directly phosphorylate plasma membrane H+-ATPase and are required for auxin-induced H+-ATPase activation, apoplastic acidification and cell expansion. Thus, our findings reveal a crucial connection between auxin and plasma membrane H+-ATPase activation in regulating apoplastic pH changes and cell expansion through TMK-based cell surface auxin signalling.
Keyphrases
  • cell wall
  • arabidopsis thaliana
  • single cell
  • cell therapy
  • cell surface
  • high glucose
  • diabetic rats
  • genome wide
  • stem cells
  • oxidative stress
  • transcription factor
  • endothelial cells
  • mesenchymal stem cells