A Role for Arabidopsis miR399f in Salt, Drought, and ABA Signaling

Mol Cells. 2016 Feb;39(2):111-8. doi: 10.14348/molcells.2016.2188. Epub 2015 Dec 15.

Abstract

MiR399f plays a crucial role in maintaining phosphate homeostasis in Arabidopsis thaliana. Under phosphate starvation conditions, AtMYB2, which plays a role in plant salt and drought stress responses, directly regulates the expression of miR399f. In this study, we found that miR399f also participates in plant responses to abscisic acid (ABA), and to abiotic stresses including salt and drought. Salt and ABA treatment induced the expression of miR399f, as confirmed by histochemical analysis of promoter-GUS fusions. Transgenic Arabidopsis plants overexpressing miR399f (miR399f-OE) exhibited enhanced tolerance to salt stress and exogenous ABA, but hypersensitivity to drought. Our in silico analysis identified ABF3 and CSP41b as putative target genes of miR399f, and expression analysis revealed that mRNA levels of ABF3 and CSP41b decreased remarkably in miR399f-OE plants under salt stress and in response to treatment with ABA. Moreover, we showed that activation of stress-responsive gene expression in response to salt stress and ABA treatment was impaired in miR399f-OE plants. Thus, these results suggested that in addition to phosphate starvation signaling, miR399f might also modulates plant responses to salt, ABA, and drought, by regulating the expression of newly discovered target genes such as ABF3 and CSP41b.

Keywords: ABA; abiotic stress; arabidopsis; drought; microRNA; salt.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abscisic Acid / metabolism
  • Abscisic Acid / pharmacology*
  • Adaptation, Physiological
  • Arabidopsis / drug effects
  • Arabidopsis / genetics*
  • Arabidopsis / metabolism
  • Arabidopsis Proteins / genetics*
  • Arabidopsis Proteins / metabolism
  • Basic-Leucine Zipper Transcription Factors / genetics*
  • Basic-Leucine Zipper Transcription Factors / metabolism
  • Droughts
  • Gene Expression Regulation, Plant*
  • Genes, Reporter
  • Globulins / genetics*
  • Globulins / metabolism
  • MicroRNAs / genetics*
  • MicroRNAs / metabolism
  • Phosphates / deficiency
  • Plants, Genetically Modified
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / metabolism
  • Salinity
  • Signal Transduction
  • Sodium Chloride / pharmacology
  • Stress, Physiological
  • Trans-Activators / genetics
  • Trans-Activators / metabolism
  • beta-Glucosidase / genetics
  • beta-Glucosidase / metabolism

Substances

  • ABF3 protein, Arabidopsis
  • Arabidopsis Proteins
  • Basic-Leucine Zipper Transcription Factors
  • Globulins
  • MIRN399 microRNA, Arabidopsis
  • MYB2 protein, Arabidopsis
  • MicroRNAs
  • Phosphates
  • Recombinant Fusion Proteins
  • Trans-Activators
  • cruciferin B, Arabidopsis
  • Sodium Chloride
  • Abscisic Acid
  • beta-Glucosidase