Molecular identification and diapause-related functional characterization of a novel dual-specificity kinase gene, MPKL, in Locusta migratoria

FEBS Lett. 2019 Nov;593(21):3064-3074. doi: 10.1002/1873-3468.13544. Epub 2019 Aug 2.

Abstract

Diapause is an important overwintering strategy enabling Locusta migratoria to survive under stressed conditions. We identified a novel dual-specificity kinase gene that is differentially expressed between long and short day-treated L. migratoria. To determine its function on photoperiodic diapause induction, we cloned the specific gene. Interestingly, phylogenetic analysis shows that this dual-specificity kinase is of the mycetozoa protein kinase-like (MPKL) type and may have been transferred horizontally from Mycetozoa to L. migratoria. RNA interference results confirm that MPKL promotes photoperiodic diapause induction of L. migratoria. Furthermore, MPKL significantly inhibits Akt and FOXO (i.e. forkhead box protein O) phosphorylation levels in ovaries, and also enhances reactive oxygen species, superoxide dismutase and catalase activities, whereas peroxidase activity is decreased under both photoperiodic regimes. The findings of the present study offer insight into the molecular mechanism responsible for dual-specificity kinase-induced diapause in insects.

Keywords: FOXO; RNAi; diapause induction; dual-specificity kinase; horizontal gene transfer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cloning, Molecular / methods*
  • Diapause
  • Evolution, Molecular
  • Female
  • Forkhead Transcription Factors / metabolism
  • Gene Transfer, Horizontal
  • Insect Proteins / genetics
  • Insect Proteins / metabolism
  • Locusta migratoria / enzymology
  • Locusta migratoria / physiology*
  • Ovary / metabolism
  • Photoperiod
  • Phylogeny
  • Protein Kinases / genetics*
  • Protein Kinases / metabolism*
  • Proto-Oncogene Proteins c-akt / metabolism

Substances

  • Forkhead Transcription Factors
  • Insect Proteins
  • Protein Kinases
  • Proto-Oncogene Proteins c-akt