Glucosinolates can act as signals to modulate intercellular trafficking via plasmodesmata

Plasmodesmata (PD) allow direct communication across the cellulosic plant cell wall, facilitating the intercellular movement of metabolites and signaling molecules within the symplast. In Arabidopsis thaliana embryos with reduced levels of the chloroplast RNA helicase ISE2, intercellular trafficking and the number of branched PD were increased. We therefore investigated the relationship between altered ISE2 expression and intercellular trafficking. Gene expression analyses in Arabidopsis tissues where ISE2 expression was increased or decreased identified genes associated with the metabolism of glucosinolates (GLSs) as highly affected. Concomitant with changes in the expression of GLS-related genes, plants with abnormal ISE2 expression contained altered GLS metabolic profiles compared with wild-type (WT) counterparts. Indeed, changes in the expression of GLS-associated genes led to altered intercellular trafficking in Arabidopsis leaves. Exogenous application of GLSs but not their breakdown products also resulted in altered intercellular trafficking. These changes in trafficking may be mediated by callose levels at PD as exogenous GLS treatment was sufficient to modulate plasmodesmal callose in WT plants. Furthermore, auxin metabolism was perturbed in plants with increased indole-type GLS levels. These findings suggest that GLSs, which are themselves transported between cells via PD, can act on PD to regulate plasmodesmal trafficking capacity.

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Publication Details

Journal
New Phytologist
Published
2025-03-17
DOI
https://doi.org/10.1111/nph.70032
Citations
2
Primary Topic
Plant Molecular Biology Research
Type
article
Field-Weighted Citation Impact
3.50

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article

Glucosinolates can act as signals to modulate intercellular trafficking via plasmodesmata

Sarbottam Piya, Tarek Hewezi, Morgan D. Strong, Jessica C. Fernandez et al.
2 citations
New Phytologist
Plant Molecular Biology Research
3.50
article

Glucosinolates can act as signals to modulate intercellular trafficking via plasmodesmata

Sarbottam Piya, Tarek Hewezi, Morgan D. Strong, Jessica C. Fernandez, Jacob O. Brunkard, Tessa M. Burch‐Smith, Min Xu, Carl E. Sams, Mohammad F. Azim, Nikki Adams
article en
2 citations

Abstract

Plasmodesmata (PD) allow direct communication across the cellulosic plant cell wall, facilitating the intercellular movement of metabolites and signaling molecules within the symplast. In Arabidopsis thaliana embryos with reduced levels of the chloroplast RNA helicase ISE2, intercellular trafficking and the number of branched PD were increased. We therefore investigated the relationship between altered ISE2 expression and intercellular trafficking. Gene expression analyses in Arabidopsis tissues where ISE2 expression was increased or decreased identified genes associated with the metabolism of glucosinolates (GLSs) as highly affected. Concomitant with changes in the expression of GLS-related genes, plants with abnormal ISE2 expression contained altered GLS metabolic profiles compared with wild-type (WT) counterparts. Indeed, changes in the expression of GLS-associated genes led to altered intercellular trafficking in Arabidopsis leaves. Exogenous application of GLSs but not their breakdown products also resulted in altered intercellular trafficking. These changes in trafficking may be mediated by callose levels at PD as exogenous GLS treatment was sufficient to modulate plasmodesmal callose in WT plants. Furthermore, auxin metabolism was perturbed in plants with increased indole-type GLS levels. These findings suggest that GLSs, which are themselves transported between cells via PD, can act on PD to regulate plasmodesmal trafficking capacity.

New PhytologistVol. 246(3)
University of Wisconsin–Madison (US), Donald Danforth Plant Science Center (US), University of Tennessee at Knoxville (US), University of California, Berkeley (US)
National Institute of General Medical Sciences, Division of Molecular and Cellular Biosciences
Openalex Percentile: Top 9%
Plant Molecular Biology Research
3.50
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