20-hydroxyecdysone mediates non-canonical regulation of mosquito vitellogenins through alternative splicing

Insect Mol Biol. 2014 Aug;23(4):407-16. doi: 10.1111/imb.12092. Epub 2014 Apr 10.

Abstract

Vitellogenesis is one of the most well-studied physiological processes in mosquitoes. Expression of mosquito vitellogenin genes is classically described as being restricted to female adult reproduction. We report premature vitellogenin transcript expression in three vector mosquitoes: Culex tarsalis, Aedes aegypti and Anopheles gambiae. Vitellogenins expressed during non-reproductive stages are alternatively spliced to retain their first intron and encode premature termination codons. We show that intron retention results in transcript degradation by translation-dependent nonsense-mediated mRNA decay. This is probably an example of regulated unproductive splicing and translation (RUST), a mechanism known to regulate gene expression in numerous organisms but which has never been described in mosquitoes. We demonstrate that the hormone 20-hydroxyecdysone (20E) is responsible for regulating post-transcriptional splicing of vitellogenin. After exposure of previtellogenic fat bodies to 20E, vitellogenin expression switches from a non-productive intron-retaining transcript to a spliced protein-coding transcript. This effect is independent of factors classically known to influence transcription, such as juvenile hormone-mediated competence and amino acid signalling through the target of rapamycin pathway. Non-canonical regulation of vitellogenesis through RUST is a novel role for the multifunctional hormone 20E, and may have important implications for general patterns of gene regulation in mosquitoes.

Keywords: 20-hydroxyecdysone; intron retention; mosquito reproduction; nonsense-mediated decay; vitellogenin.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Aedes / genetics
  • Aedes / growth & development
  • Aedes / metabolism
  • Alternative Splicing*
  • Animals
  • Anopheles / genetics
  • Anopheles / growth & development
  • Anopheles / metabolism
  • Culex / genetics
  • Culex / growth & development
  • Culex / metabolism
  • Culicidae / genetics*
  • Culicidae / growth & development
  • Culicidae / metabolism
  • Ecdysterone / metabolism*
  • Fat Body / metabolism
  • Female
  • Gene Expression Regulation, Developmental*
  • Insect Proteins / genetics
  • Insect Proteins / metabolism
  • Insect Vectors
  • Larva / genetics
  • Larva / metabolism
  • Male
  • Pupa / genetics
  • Pupa / metabolism
  • RNA, Messenger
  • Vitellogenesis / genetics
  • Vitellogenins / genetics
  • Vitellogenins / metabolism

Substances

  • Insect Proteins
  • RNA, Messenger
  • Vitellogenins
  • Ecdysterone