4.6 Article

MEDIATOR16 orchestrates local and systemic responses to phosphate scarcity in Arabidopsis roots

Journal

NEW PHYTOLOGIST
Volume 229, Issue 3, Pages 1278-1288

Publisher

WILEY
DOI: 10.1111/nph.16989

Keywords

Arabidopsis thaliana; malate; Mediator complex; phosphate starvation; plant nutrition; root system architecture

Categories

Funding

  1. CONACyT Fronteras fund [137-2015]
  2. Governor University Research Initiative program from the State of Texas [05-2018]
  3. Howard Hughes Medical Institute [55005946]

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This study assessed the role of the MED16 subunit in Arabidopsis root system remodeling in response to phosphate limitation, showing that it modulates the expression of a large set of low-phosphate-induced genes to increase phosphate absorption in roots. The findings suggest that MED16 is critical for the transcriptional activation of STOP1 targets, including the membrane permease ALMT1, in order to enhance malate exudation in response to low phosphate, shedding light on how plant cells orchestrate root morphogenesis to gene expression with the STOP1-ALMT1 module.
Phosphate (P-i) is a critical macronutrient for the biochemical and molecular functions of cells. Under phosphate limitation, plants manifest adaptative strategies to increase phosphate scavenging. However, how low phosphate sensing links to the transcriptional machinery remains unknown. The role of the MEDIATOR (MED) transcriptional co-activator, through its MED16 subunit in Arabidopsis root system architecture remodeling in response to phosphate limitation was assessed. Its critical function acting over the SENSITIVE TO PROTON RHIZOTOXICITY1 (STOP1)-ALUMINUM-ACTIVATED MALATE TRANSPORT1 (ALMT1) signaling module was tested through a combination of genetic, biochemical, and genome-wide transcriptomic approaches. Root system configuration in response to phosphate scarcity involved MED16 functioning, which modulates the expression of a large set of low-phosphate-induced genes that respond to local and systemic signals in the Arabidopsis root tip, including those directly activated by STOP1. Biomolecular fluorescence complementation analysis suggests that MED16 is required for the transcriptional activation of STOP1 targets, including the membrane permease ALMT1, to increase malate exudation in response to low phosphate. Our results unveil the function of a critical transcriptional component, MED16, in the root adaptive responses to a scarce plant macronutrient, which helps understanding how plant cells orchestrate root morphogenesis to gene expression with the STOP1-ALMT1 module.

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