Cell wall patterning regulates plant stem cell dynamics

The plant cell wall regulates development through spatiotemporal modulation of its chemical and mechanical properties. Pectin methylesterification is recognized as a rheological switch controlling wall stiffness. Here, we reveal a bimodal methylesterification pattern in the shoot meristem: Mature walls exhibit high methylesterification, whereas demethylesterified pectins are deposited at new cross walls. This spatial heterogeneity is established through nuclear sequestration of <i>PECTIN METHYLESTERASE5</i> (<i>PME5</i>) mRNA. MYB3R4-driven transcription, combined with RZ-1B/1C-mediated retention, creates a mitotically associated <i>PME5</i> mRNA reservoir in the nucleus. Nuclear envelope disassembly synchronizes <i>PME5</i> messenger RNA (mRNA) release with cell plate formation, enabling precise demethylesterification at division planes. Perturbation of this spatial control compromises stem cell maintenance or breaks division patterning. Our study uncovers an mRNA compartmentalization mechanism that couples stem cell dynamics with pectin modification.

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Publication Details

Journal
Science
Published
2025-12-04
DOI
https://doi.org/10.1126/science.ady4102
Citations
3
Primary Topic
Polysaccharides and Plant Cell Walls
Type
article
Field-Weighted Citation Impact
5.25
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article

Cell wall patterning regulates plant stem cell dynamics

Han Han, Yimin Gu, Wenjuan Cai, Mingjun Gao et al.
3 citations
Science
Polysaccharides and Plant Cell Walls
5.25
article

Cell wall patterning regulates plant stem cell dynamics

Han Han, Yimin Gu, Wenjuan Cai, Mingjun Gao, Yimin Zhu, Raymond Wightman, Weibing Yang, Miao Lan, Yiliang Ding, Yangxuan Liu, Yihao Fu, Xianmiao Zhu, Guanghua Gao, Xing Chen
article en
3 citations

Abstract

The plant cell wall regulates development through spatiotemporal modulation of its chemical and mechanical properties. Pectin methylesterification is recognized as a rheological switch controlling wall stiffness. Here, we reveal a bimodal methylesterification pattern in the shoot meristem: Mature walls exhibit high methylesterification, whereas demethylesterified pectins are deposited at new cross walls. This spatial heterogeneity is established through nuclear sequestration of <i>PECTIN METHYLESTERASE5</i> (<i>PME5</i>) mRNA. MYB3R4-driven transcription, combined with RZ-1B/1C-mediated retention, creates a mitotically associated <i>PME5</i> mRNA reservoir in the nucleus. Nuclear envelope disassembly synchronizes <i>PME5</i> messenger RNA (mRNA) release with cell plate formation, enabling precise demethylesterification at division planes. Perturbation of this spatial control compromises stem cell maintenance or breaks division patterning. Our study uncovers an mRNA compartmentalization mechanism that couples stem cell dynamics with pectin modification.

ScienceVol. 390(6777)
John Innes Centre (GB), Nanjing Forestry University (CN), Chinese Academy of Sciences (CN), University of Cambridge (GB), Fudan University (CN), Norwich Research Park (GB), Sainsbury Laboratory (GB), Center for Excellence in Molecular Plant Sciences (CN), University of Chinese Academy of Sciences (CN)
Openalex Percentile: Top 5%
Polysaccharides and Plant Cell Walls
5.25
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