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TMK-based cell-surface auxin signalling activates cell-wall acidification
The phytohormone auxin controls many processes in plants, at least in part through its regulation of cell expansion(1). 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...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8549421/ https://www.ncbi.nlm.nih.gov/pubmed/34707287 http://dx.doi.org/10.1038/s41586-021-03976-4 |
Sumario: | The phytohormone auxin controls many processes in plants, at least in part through its regulation of cell expansion(1). 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 apoplast(2), 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. |
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