Brassica Rapa SR45a Regulates Drought Tolerance via the Alternative Splicing of Target Genes

Genes (Basel). 2020 Feb 10;11(2):182. doi: 10.3390/genes11020182.

Abstract

The emerging evidence has shown that plant serine/arginine-rich (SR) proteins play a crucial role in abiotic stress responses by regulating the alternative splicing (AS) of key genes. Recently, we have shown that drought stress enhances the expression of SR45a (also known as SR-like 3) in Brassica rapa. Herein, we unraveled the hitherto unknown functions of BrSR45a in drought stress response by comparing the phenotypes, chlorophyll a fluorescence and splicing patterns of the drought-responsive genes of Arabidopsis BrSR45a overexpressors (OEs), homozygous mutants (SALK_052345), and controls (Col-0). Overexpression and loss of function did not result in aberrant phenotypes; however, the overexpression of BrSR45a was positively correlated with drought tolerance and the stress recovery rate in an expression-dependent manner. Moreover, OEs showed a higher drought tolerance index during seed germination (38.16%) than the control lines. Additionally, the overexpression of BrSR45a induced the expression of the drought stress-inducible genes RD29A, NCED3, and DREB2A under normal conditions. To further illustrate the molecular linkages between BrSR45a and drought tolerance, we investigated the AS patterns of key drought-tolerance and BrSR45a interacting genes in OEs, mutants, and controls under both normal and drought conditions. The splicing patterns of DCP5, RD29A, GOLS1, AKR, U2AF, and SDR were different between overexpressors and mutants under normal conditions. Furthermore, drought stress altered the splicing patterns of NCED2, SQE, UPF1, U4/U6-U5 tri-snRNP-associated protein, and UPF1 between OEs and mutants, indicating that both overexpression and loss of function differently influenced the splicing patterns of target genes. This study revealed that BrSR45a regulates the drought stress response via the alternative splicing of target genes in a concentration-dependent manner.

Keywords: BrSR-like 3; alternative splicing; drought tolerance; serine/arginine-rich proteins; thermotolerance.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptation, Physiological / genetics*
  • Alcohol Oxidoreductases / genetics
  • Alcohol Oxidoreductases / metabolism
  • Alternative Splicing / genetics*
  • Arabidopsis
  • Arabidopsis Proteins / genetics
  • Arabidopsis Proteins / metabolism
  • Ascorbate Peroxidases / genetics
  • Ascorbate Peroxidases / metabolism
  • Brassica rapa / genetics*
  • Cell Cycle Proteins / genetics
  • Cell Cycle Proteins / metabolism
  • Chlorophyll / chemistry
  • Co-Repressor Proteins / genetics
  • Co-Repressor Proteins / metabolism
  • Dioxygenases / genetics
  • Dioxygenases / metabolism
  • Droughts
  • Galactosyltransferases / genetics
  • Galactosyltransferases / metabolism
  • Gene Expression Regulation, Plant / genetics
  • Germination / genetics*
  • Oxidative Stress / genetics
  • Phenotype
  • Phylogeny
  • Plant Proteins / genetics
  • Plant Proteins / metabolism
  • Plants, Genetically Modified
  • RNA Helicases / genetics
  • RNA Helicases / metabolism
  • Stress, Physiological / genetics*
  • Superoxide Dismutase-1 / genetics
  • Superoxide Dismutase-1 / metabolism
  • Thermotolerance / genetics
  • Up-Regulation

Substances

  • Arabidopsis Proteins
  • AtGR1 protein, Arabidopsis
  • Cell Cycle Proteins
  • Co-Repressor Proteins
  • DCP5 protein, Arabidopsis
  • KIN1 protein, Arabidopsis
  • Plant Proteins
  • RD29a protein, Arabidopsis
  • Chlorophyll
  • Alcohol Oxidoreductases
  • menthone (3S)-neomenthol reductase, Arabidopsis
  • APX1 protein, Arabidopsis
  • Ascorbate Peroxidases
  • Dioxygenases
  • 9-cis-epoxy-carotenoid dioxygenase
  • Superoxide Dismutase-1
  • Galactosyltransferases
  • GolS1 protein, Arabidopsis
  • UPF1 protein, Arabidopsis
  • RNA Helicases