Mosquito-specific microRNA-1890 targets the juvenile hormone-regulated serine protease JHA15 in the female mosquito gut

RNA Biol. 2015;12(12):1383-90. doi: 10.1080/15476286.2015.1101525.

Abstract

Females of the hematophagous mosquito species require a vertebrate blood meal to supply amino acids and other nutrients necessary for egg development, serving as the driving force for the spread of many vector-borne diseases in humans. Blood digestion utilizes both early and late phase serine proteases (SPs) that are differentially regulated at the transcriptional and post-transcriptional level. To uncover the regulatory complexity of SPs in the female mosquito midgut, we investigated involvement of miRNAs in regulating the juvenile hormone (JH)-controlled chymotrypsin-like SP, JHA15. We identified regulatory regions complementary to the mosquito-specific miRNA, miR-1890, within the 3' UTR of JHA15 mRNA. The level of the JHA15 transcript is highest post eclosion and drastically declines post blood meal (PBM), exhibiting an opposite trend to miR-1890 that peaks at 24 h PBM. Depletion of miR-1890 results in defects in blood digestion, ovary development and egg deposition. JHA15 mRNA and protein levels are elevated in female mosquitoes with miR-1890 inhibition. JHA15 RNA interference in the miR-1890 depletion background alleviates miR-1890 depletion phenotypes. The miR-1890 gene is activated by the 20-hydroxyecdysone pathway that involves the ecdysone receptor and the early genes, E74B and Broad Z2. Our study suggests that miR-1890 controls JHA15 mRNA stability in a stage- and tissue- specific manner.

Keywords: Mosquito; digestive protease; ecdysone; juvenile hormone; microRNA.

Publication types

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

MeSH terms

  • 3' Untranslated Regions / genetics
  • Aedes / enzymology*
  • Aedes / genetics*
  • Animals
  • Binding Sites
  • Digestion
  • Digestive System / enzymology*
  • Ecdysone / metabolism
  • Female
  • Gene Expression Regulation
  • Gene Knockdown Techniques
  • Insect Proteins / genetics
  • Juvenile Hormones / metabolism*
  • MicroRNAs / metabolism*
  • Phenotype
  • RNA Interference
  • Serine Proteases / metabolism*
  • Signal Transduction / genetics
  • Species Specificity

Substances

  • 3' Untranslated Regions
  • Insect Proteins
  • Juvenile Hormones
  • MicroRNAs
  • Ecdysone
  • Serine Proteases