# Plasticity of Root Architecture and ROS–Auxin Regulation in Paeonia ostii Under Root-Zone Restriction

**Authors:** Qiang Xing, Ruotong Zhao, Peng Zhou, Jun Qin, Heming Liu, Shuiyan Yu, Bin Zhao, Yonghong Hu

PMC · DOI: 10.3390/plants14121889 · Plants · 2025-06-19

## TL;DR

This study explores how root zone restriction affects the root structure and stress responses in Paeonia ostii, revealing how plants adapt to limited space.

## Contribution

The study introduces new insights into the plasticity of root architecture and the role of ROS–auxin interactions in Paeonia ostii under root zone restriction.

## Key findings

- Root zone restriction increased the root-to-shoot ratio by 44.8%, reallocating carbon to enhance root growth.
- Optimal root efficiency was observed at 26.09–28.23 L container volumes, with increased root length and branching.
- RZR disrupted H2O2 homeostasis and upregulated auxin transporter genes, suggesting a ROS–auxin crosstalk mechanism.

## Abstract

Root zone restriction (RZR) technology optimizes plant growth and quality. However, the fleshy root system of Paeonia ostii exhibits sensitivity to spatial constraints, and research on the plasticity of its root architecture and adaptation mechanisms remains inadequate. This study provides a functional analysis of biomass allocation and root architectural responses to the root-zone restriction (RZR) in P. ostii, comparing three container volumes (8.5, 17, and 34 L). While the total biomass increased with root zone volume (e.g., shoot biomass rose from 9.30 g to 59.94 g), RZR induced a 44.8% increase in root-to-shoot ratio, indicating carbon reallocation to enhance belowground resource acquisition. The principal component analysis identified root biomass, volume, and surface area as key plasticity drivers. Optimal root efficiency occurred at 26.09–28.23 L, where root length and tip/fork numbers peaked. Mechanistically, RZR elevated superoxide dismutase (SOD) activity by 49.74% but reduced catalase (CAT) by 74.24%, disrupting H2O2 homeostasis. Concurrently, auxin transporter genes (PIN1, AUX1) were upregulated, promoting root elongation and lateral branching through auxin redistribution. We hypothesize that ROS–auxin crosstalk mediates architectural reconfiguration to mitigate spatial stress, with thickened roots enhancing structural stability in restricted environments. The study underscores the need to optimize root zone volume in woody species cultivation, providing thresholds (e.g., >28 L for mature plants) to balance biomass yield and physiological costs in horticultural management.

## Linked entities

- **Genes:** PIN1 (peptidylprolyl cis/trans isomerase, NIMA-interacting 1) [NCBI Gene 5300], AUX1 (Transmembrane amino acid transporter family protein) [NCBI Gene 818390]
- **Proteins:** Cat (Catalase)
- **Chemicals:** H2O2 (PubChem CID 784)
- **Species:** Paeonia ostii (taxon 459177)

## Full-text entities

- **Chemicals:** carbon (MESH:D002244), ROS-Auxin (-), O (MESH:D010100), H (MESH:D006859), auxin (MESH:D007210)
- **Species:** Paeonia ostii (species) [taxon 459177]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12196556/full.md

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12196556/full.md

## References

50 references — full list in the complete paper: https://tomesphere.com/paper/PMC12196556/full.md

---
Source: https://tomesphere.com/paper/PMC12196556