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Evidence for the Regulation of Gynoecium Morphogenesis by Via Cell Wall Dynamics

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Journal Plant Physiol
Specialty Physiology
Date 2018 Sep 22
PMID 30237208
Citations 12
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Abstract

() is an atypical member of the AUXIN RESPONSE FACTOR family of transcription factors that plays a crucial role in tissue patterning in the Arabidopsis () gynoecium. Though recent insights have provided valuable information on ETT's interactions with other components of auxin signaling, the biophysical mechanisms linking ETT to its ultimate effects on gynoecium morphology were until now unknown. Here, using techniques to assess cell-wall dynamics during gynoecium growth and development, we provide a coherent body of evidence to support a model in which ETT controls the elongation of the valve tissues of the gynoecium through the positive regulation of pectin methylesterase (PME) activity in the cell wall. This increase in PME activity results in an increase in the level of demethylesterified pectins and a consequent reduction in cell wall stiffness, leading to elongation of the valves. Though similar biophysical mechanisms have been shown to act in the stem apical meristem, leading to the expansion of organ primordia, our findings demonstrate that regulation of cell wall stiffness through the covalent modification of pectin also contributes to tissue patterning within a developing plant organ.

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References
1.
Hawkins C, Liu Z . A model for an early role of auxin in Arabidopsis gynoecium morphogenesis. Front Plant Sci. 2014; 5:327. PMC: 4086399. DOI: 10.3389/fpls.2014.00327. View

2.
Simonini S, Bencivenga S, Trick M, Ostergaard L . Auxin-Induced Modulation of ETTIN Activity Orchestrates Gene Expression in Arabidopsis. Plant Cell. 2017; 29(8):1864-1882. PMC: 5590509. DOI: 10.1105/tpc.17.00389. View

3.
Guilfoyle T, Hagen G . Auxin response factors. Curr Opin Plant Biol. 2007; 10(5):453-60. DOI: 10.1016/j.pbi.2007.08.014. View

4.
Pekker I, Alvarez J, Eshed Y . Auxin response factors mediate Arabidopsis organ asymmetry via modulation of KANADI activity. Plant Cell. 2005; 17(11):2899-910. PMC: 1276018. DOI: 10.1105/tpc.105.034876. View

5.
Szymanska-Chargot M, Zdunek A . Use of FT-IR Spectra and PCA to the Bulk Characterization of Cell Wall Residues of Fruits and Vegetables Along a Fraction Process. Food Biophys. 2013; 8(1):29-42. PMC: 3593005. DOI: 10.1007/s11483-012-9279-7. View