Dual role of BdMUTE during stomatal development in the model grass Brachypodium distachyon.

Grasses form morphologically derived, four-celled stomata, where two dumbbell-shaped guard cells (GCs) are flanked by two lateral subsidiary cells (SCs). This innovative form enables rapid opening and closing kinetics and efficient plant-atmosphere gas exchange. The mobile bHLH transcription factor MUTE is required for SC formation in grasses. Yet, if and how MUTE also regulates GC development and if MUTE mobility is required for SC recruitment is unclear. Here, we transgenically impaired BdMUTE mobility from GC to SC precursors in the emerging model grass Brachypodium distachyon. Our data indicates that reduced BdMUTE mobility severely affected the spatiotemporal coordination of GC and SC development. Furthermore, while BdMUTE has a cell-autonomous role in GC division orientation, complete dumbbell morphogenesis of GCs required SC recruitment. Finally, leaf-level gas exchange measurements showed that dosage-dependent complementation of the four-celled grass morphology was mirrored in a gradual physiological complementation of stomatal kinetics. Together, our work revealed a dual role of grass MUTE in regulating GC division orientation and SC recruitment, which in turn was required for GC morphogenesis and the rapid kinetics of grass stomata.

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Publication Details

Journal
Open Access CRIS of the University of Bern
Published
2024-10-15
DOI
https://doi.org/10.48350/199904
Primary Topic
Plant Molecular Biology Research
Type
article
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article

Dual role of BdMUTE during stomatal development in the model grass Brachypodium distachyon.

Open Access CRIS of the University of Bern
Plant Molecular Biology Research
article

Dual role of BdMUTE during stomatal development in the model grass Brachypodium distachyon.

article en

Abstract

Grasses form morphologically derived, four-celled stomata, where two dumbbell-shaped guard cells (GCs) are flanked by two lateral subsidiary cells (SCs). This innovative form enables rapid opening and closing kinetics and efficient plant-atmosphere gas exchange. The mobile bHLH transcription factor MUTE is required for SC formation in grasses. Yet, if and how MUTE also regulates GC development and if MUTE mobility is required for SC recruitment is unclear. Here, we transgenically impaired BdMUTE mobility from GC to SC precursors in the emerging model grass Brachypodium distachyon. Our data indicates that reduced BdMUTE mobility severely affected the spatiotemporal coordination of GC and SC development. Furthermore, while BdMUTE has a cell-autonomous role in GC division orientation, complete dumbbell morphogenesis of GCs required SC recruitment. Finally, leaf-level gas exchange measurements showed that dosage-dependent complementation of the four-celled grass morphology was mirrored in a gradual physiological complementation of stomatal kinetics. Together, our work revealed a dual role of grass MUTE in regulating GC division orientation and SC recruitment, which in turn was required for GC morphogenesis and the rapid kinetics of grass stomata.

Open Access CRIS of the University of Bern
Planta (RU), Institute of Plant Biology (HU)
Openalex Percentile: Top 31%
Plant Molecular Biology Research
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Dual role of BdMUTE during stomatal development in the model grass Brachypodium distachyon. · Open Access CRIS of the University of Bern (2024) | TGRS Research Map | TGRS