IPA1 Negatively Regulates Early Rice Seedling Development by Interfering with Starch Metabolism via the GA and WRKY Pathways

Int J Mol Sci. 2021 Jun 20;22(12):6605. doi: 10.3390/ijms22126605.

Abstract

Ideal Plant Architecture 1 (IPA1) encodes SQUAMOSA PROMOTER BINDING PROTEIN-LIKE 14 (SPL14) with a pleiotropic effect on regulating rice development and biotic stress responses. To investigate the role of IPA1 in early seedling development, we developed a pair of IPA1/ipal-NILs and found that seed germination and early seedling growth were retarded in the ipa1-NIL. Analysis of the soluble sugar content, activity of amylase, and expression of the α-amylase genes revealed that the starch metabolism was weakened in the ipa1-NIL germinating seeds. Additionally, the content of bioactive gibberellin (GA) was significantly lower than that in the IPA1-NIL seeds at 48 h of imbibition. Meanwhile, the expression of GA synthesis-related gene OsGA20ox1 was downregulated, whereas the expression of GA inactivation-related genes was upregulated in ipa1-NIL seeds. In addition, the expression of OsWRKY51 and OsWRKY71 was significantly upregulated in ipa1-NIL seeds. Using transient dual-luciferase and yeast one-hybrid assays, IPA1 was found to directly activate the expression of OsWRKY51 and OsWRKY71, which would interfere with the binding affinity of GA-induced transcription factor OsGAMYB to inhibit the expression of α-amylase genes. In summary, our results suggest that IPA1 negatively regulates seed germination and early seedling growth by interfering with starch metabolism via the GA and WRKY pathways.

Keywords: IPA1/OsSPL14; WRKY; gibberellin (GA); rice (Oryza sativa L.); seed germination.

MeSH terms

  • DNA-Binding Proteins / metabolism*
  • Gene Expression Regulation, Plant
  • Germination / genetics
  • Gibberellins / metabolism*
  • Oryza / physiology*
  • Phenotype
  • Plant Development*
  • Protein Binding
  • Seedlings / growth & development*
  • Signal Transduction*
  • Starch / metabolism*
  • Transcription Factors / metabolism*
  • alpha-Amylases / metabolism

Substances

  • DNA-Binding Proteins
  • Gibberellins
  • Transcription Factors
  • Starch
  • alpha-Amylases