AFB1 controls rapid auxin signalling through membrane depolarization in Arabidopsis thaliana root.

Abstract

Membrane potential reflects the difference between cytoplasmic and apoplastic electrical potentials and is essential for cellular operation. The application of the phytohormone auxin (IAA) causes instantaneous membrane depolarization in various cell types1–6, making depolarization a hallmark of IAA-induced rapid responses. In root hairs, depolarization requires functional IAA transport and TIR1/AFB signalling5 but its physiological significance is not understood. Specifically in roots, auxin triggers rapid growth inhibition7–9 (RGI); a process required for gravitropic bending. RGI is initiated by the TIR1/AFB co-receptors, AFB1 paralogue playing a crucial role10,11. The nature of the underlying rapid signalling is unknown, as well as the molecular machinery executing it. Even though the growth and depolarization responses to auxin show remarkable similarities, the significance of membrane depolarization for root growth inhibition and gravitropism is unclear. Here, by combining the DISBAC2(3) voltage sensor with microfluidics and vertical-stage microscopy, we show that rapid auxin-induced membrane depolarization tightly correlates with rapid RGI. Rapid depolarization and RGI require the AFB1 auxin co-receptor. Finally, AFB1 is essential for the rapid formation of membrane depolarization gradient across the gravistimulated root. These results clarify the role of AFB1 as the central receptor for rapid auxin responses.