EAT1 promotes tapetal cell death by regulating aspartic proteases during male reproductive development in rice

Nat Commun. 2013:4:1445. doi: 10.1038/ncomms2396.

Abstract

Programmed cell death is essential for the development of multicellular organisms, yet pathways of plant programmed cell death and its regulation remain elusive. Here we report that ETERNAL TAPETUM 1, a basic helix-loop-helix transcription factor conserved in land plants, positively regulates programmed cell death in tapetal cells in rice anthers. eat1 exhibits delayed tapetal cell death and aborted pollen formation. ETERNAL TAPETUM 1 directly regulates the expression of OsAP25 and OsAP37, which encode aspartic proteases that induce programmed cell death in both yeast and plants. Expression and genetic analyses revealed that ETERNAL TAPETUM 1 acts downstream of TAPETUM DEGENERATION RETARDATION, another positive regulator of tapetal programmed cell death, and that ETERNAL TAPETUM 1 can also interact with the TAPETUM DEGENERATION RETARDATION protein. This study demonstrates that ETERNAL TAPETUM 1 promotes aspartic proteases triggering plant programmed cell death, and reveals a dynamic regulatory cascade in male reproductive development in rice.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Aspartic Acid Proteases / metabolism*
  • Base Sequence
  • Basic Helix-Loop-Helix Transcription Factors / chemistry
  • Basic Helix-Loop-Helix Transcription Factors / genetics
  • Basic Helix-Loop-Helix Transcription Factors / metabolism
  • Cell Death
  • Chromosomes, Plant / genetics
  • Gene Expression Regulation, Plant
  • Genes, Plant / genetics
  • Models, Biological
  • Molecular Sequence Data
  • Mutation / genetics
  • Organ Specificity
  • Oryza / cytology*
  • Oryza / enzymology*
  • Oryza / genetics
  • Oryza / ultrastructure
  • Phenotype
  • Phylogeny
  • Physical Chromosome Mapping
  • Plant Proteins / chemistry*
  • Plant Proteins / genetics
  • Plant Proteins / metabolism
  • Pollen / cytology*
  • Pollen / enzymology*
  • Pollen / ultrastructure
  • Protein Binding
  • Reproduction
  • Saccharomyces cerevisiae / cytology
  • Saccharomyces cerevisiae / metabolism

Substances

  • Basic Helix-Loop-Helix Transcription Factors
  • Plant Proteins
  • Aspartic Acid Proteases