The effect of E93 knockdown on female reproduction in the red flour beetle, Tribolium castaneum

Arch Insect Biochem Physiol. 2020 Aug;104(4):e21688. doi: 10.1002/arch.21688. Epub 2020 May 11.

Abstract

The E93 transcription factor is a member of helix-turn-helix transcription factor family containing a Pip-squeak motif. This ecdysone primary response gene was identified as a regulator of cell death in Drosophila melanogaster where it is involved in ecdysone-induced autophagy and caspase activity that mediate degeneration of larval tissues during metamorphosis from larva to pupa. However, its function in adult insects is not well studied. To study E93 function in the red flour beetle, Tribolium castaneum, double-stranded RNA (dsRNA) targeting E93 (dsE93) was injected into newly emerged adults. Knockdown of E93 caused a decrease in the synthesis of vitellogenin (Vg), oocyte development, and egg-laying. Sequencing of RNA isolated from adults injected with dsE93 and control dsmalE (dsRNA targeting Escherichia coli malE gene) followed by differential gene expression analysis showed upregulation of genes involved in the metabolism of reserved nutrients. E93 knockdown induced changes in gene expression resulted in a decrease in Vg synthesis in the fat body and oocyte maturation in ovaries. Mating experiments showed that females injected with dsE93 did not lay eggs. Knockdown of E93 caused a reduction in the number and size of lipid droplets in the fat body when compared with that in control beetles injected with dsmalE. These data suggest that during the first 2-3 days after the emergence of adult females, E93 suppresses genes coding for enzymes that metabolize reserved nutrients until initiation of vitellogenesis and oogenesis.

Keywords: E93; RNAi; Tribolium; reproduction; vitellogenesis.

MeSH terms

  • Animals
  • Fat Body
  • Female
  • Gene Expression Profiling
  • Insect Proteins / genetics
  • Insect Proteins / metabolism
  • Male
  • Oogenesis
  • Oviposition
  • RNA, Double-Stranded*
  • Transcription Factors / genetics*
  • Tribolium / genetics*
  • Tribolium / metabolism*
  • Vitellogenesis

Substances

  • Insect Proteins
  • RNA, Double-Stranded
  • Transcription Factors