4.8 Article

Cell surface and intracellular auxin signalling for H+ fluxes in root growth

Journal

NATURE
Volume 599, Issue 7884, Pages 273-+

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41586-021-04037-6

Keywords

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Funding

  1. European Research Council Advanced Grant [ETAP-742985]
  2. Austrian Science Fund (FWF) [I 3630-B25]
  3. National Institutes of Health [GM067203]
  4. Netherlands Organization for Scientific Research (NWO) [VIDI-864.13.001]
  5. Research Foundation-Flanders (FWO) [Odysseus II G0D0515N]
  6. European Research Council Starting Grant [TORPEDO-714055]
  7. VICI grant from Netherlands Organization for Scientific Research [865.14.001]
  8. Australian Research Council
  9. China National Distinguished Expert Project [WQ20174400441]
  10. MEXT/JSPS KAKENHI [20K06685, 20H05687, 20H05910]
  11. European Union's Horizon 2020 research and innovation programme under Marie Sklodowska-Curie grant [665385]
  12. DOC Fellowship of the Austrian Academy of Sciences
  13. China Scholarship Council
  14. Grants-in-Aid for Scientific Research [20K06685, 20H05687] Funding Source: KAKEN

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Plant growth is regulated by environmental factors, such as how plants respond to gravity by bending shoots up and roots down. Research has shown that the plant hormone auxin affects root growth by regulating cell expansion and contraction in the roots.
Growth regulation tailors development in plants to their environment. A prominent example of this is the response to gravity, in which shoots bend up and roots bend down(1). This paradox is based on opposite effects of the phytohormone auxin, which promotes cell expansion in shoots while inhibiting it in roots via a yet unknown cellular mechanism(2). Here, by combining microfluidics, live imaging, genetic engineering and phosphoproteomics in Arabidopsis thaliana, we advance understanding of how auxin inhibits root growth. We show that auxin activates two distinct, antagonistically acting signalling pathways that converge on rapid regulation of apoplastic pH, a causative determinant of growth. Cell surface-based TRANSMEMBRANE KINASE1 (TMK1) interacts with and mediates phosphorylation and activation of plasma membrane H+-ATPases for apoplast acidification, while intracellular canonical auxin signalling promotes net cellular H+ influx, causing apoplast alkalinization. Simultaneous activation of these two counteracting mechanisms poises roots for rapid, fine-tuned growth modulation in navigating complex soil environments.

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