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February 2, 2026Proceedings of the National Academy of Sciences3 citationsOpen Access

PLETHORA–autophagy axis activates organ regeneration through ROS modulation

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AGAkansha GangulyAHAabha HumnabadkarKGKomal Gautam

Key Points

  • To explore how autophagy aids in cellular homeostasis and wound repair in plants.
  • Examined the role of autophagy-related gene ATG8 in root regeneration.
  • Analyzed the function of PLETHORA transcription factors in regulating ATG8.
  • Investigated the impact of disrupting the PLT–ATG8 regulatory axis on stress and regeneration.
  • Transcription of ATG8 genes is essential for de novo root regeneration.
  • Disruption of the PLT–ATG8 axis led to increased intracellular stress.
  • Maintaining optimal levels of reactive oxygen species is crucial for successful regeneration.

Abstract

Injury-induced disruption of cellular homeostasis leads to accumulation of stress at sites adjacent to a wound. How do these cells mitigate wound-induced stress and restore cellular homeostasis to promote regeneration? To address this question, we examined the role of autophagy—a conserved quality control pathway that recycles defective cellular components to sustain cellular homeostasis—in facilitating wound repair in plants. We demonstrate that transcriptional activation of autophagy-related gene 8 ( ATG8 ) genes is essential for de novo root regeneration, but dispensable for wound induced callus formation from an excised leaf. Plant-specific transcription factors PLETHORA (PLT) activate the transcription of a subset of ATG8 genes and function nonredundantly in this process. Disrupting the PLT– ATG8 regulatory axis severely impairs organelle turnover, resulting in increased intracellular stress and ectopic accumulation of reactive oxygen species (ROS). PLT– ATG8 mediated positioning of optimal ROS levels promotes the expression of stem-cell regulators for successful de novo root regeneration. Altogether, our findings illustrate how plants utilize kingdom-specific developmental regulators, such as PLTs, to activate evolutionarily conserved pathways, effectively managing wound-induced cellular stress and facilitating organ regeneration.

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Cite This Study

Ganguly et al. (2026) studied this question.

synapsesocial.com/papers/6980ffa4c1c9540dea81244ehttps://doi.org/10.1073/pnas.2513954123
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