Wheat TaSPL8 Modulates Leaf Angle Through Auxin and Brassinosteroid Signaling

Plant Physiol. 2019 Sep;181(1):179-194. doi: 10.1104/pp.19.00248. Epub 2019 Jun 17.

Abstract

In grass crops, leaf angle is determined by development of the lamina joint, the tissue connecting the leaf blade and sheath, and is closely related to crop architecture and yield. In this study, we identified a mutant generated by fast neutron radiation that exhibited an erect leaf phenotype caused by defects in lamina joint development. Map-based cloning revealed that the gene TaSPL8, encoding a SQUAMOSA PROMOTER BINDING-LIKE (SPL) protein, is deleted in this mutant. TaSPL8 knock-out mutants exhibit erect leaves due to loss of the lamina joint, compact architecture, and increased spike number especially in high planting density, suggesting similarity with its LIGULESS1 homologs in maize (Zea mays) and rice (Oryza sativa). Hence, LG1 could be a robust target for plant architecture improvement in grass species. Common wheat (Triticum aestivum, 2n = 6× = 42; BBAADD) is an allohexaploid containing A, B, and D subgenomes and the homeologous gene of TaSPL8 from the D subgenome contributes to the length of the lamina joint to a greater extent than that from the A and B subgenomes. Comparison of the transcriptome between the Taspl8 mutant and the wild type revealed that TaSPL8 is involved in the activation of genes related to auxin and brassinosteroid pathways and cell elongation. TaSPL8 binds to the promoters of the AUXIN RESPONSE FACTOR gene and of the brassinosteroid biogenesis gene CYP90D2 and activates their expression. These results indicate that TaSPL8 might regulate lamina joint development through auxin signaling and the brassinosteroid biosynthesis pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Brassinosteroids / metabolism*
  • Gene Expression Regulation, Plant
  • Indoleacetic Acids / metabolism*
  • Phenotype
  • Plant Growth Regulators / metabolism*
  • Plant Leaves / genetics
  • Plant Leaves / growth & development
  • Plant Leaves / physiology
  • Plant Proteins / genetics
  • Plant Proteins / metabolism*
  • Promoter Regions, Genetic / genetics
  • Signal Transduction
  • Transcriptome*
  • Triticum / genetics*
  • Triticum / growth & development
  • Triticum / physiology

Substances

  • Brassinosteroids
  • Indoleacetic Acids
  • Plant Growth Regulators
  • Plant Proteins