Live imaging reveals that cytosolic calcium integrates multiple stimuli for root growth regulation, suggesting a common signaling mechanism.
Roots must continuously adapt their growth and have evolved the ability to rapidly respond to diverse environmental and hormonal cues, including the phytohormone auxin. Auxin-induced cellular responses involve membrane depolarization, cytosolic calcium (Ca 2+ ) elevation, and extracellular pH increase, but how these processes lead to rapid growth regulation remains unclear. Here, we show that cytosolic Ca 2+ acts as a universal signal integrating diverse cues for the rapid regulation of root growth. Using live imaging, microfluidics, and optogenetics in Arabidopsis, we demonstrate that a swift rise in cytosolic Ca 2+ is the primary target of auxin signaling affecting growth inhibition. Disruption of Ca 2+ influx abolishes these responses, whereas light-gated Ca 2+ influx from the apoplast or endoplasmic reticulum stores inhibits growth. Multiple unrelated stimuli−including auxin, extracellular ATP, RALF peptides, and hydrogen peroxide − converge on this Ca2+ -dependent mechanism. Cytosolic Ca 2+ ; elevation thus represents a necessary and sufficient step for rapid growth inhibition, revealing a unifying principle of root signaling.
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Randuch et al. (2025) studied this question.
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