Tyrosine Hydroxylase is crucial for maintaining pupal tanning and immunity in Anopheles sinensis

Sci Rep. 2016 Jul 15:6:29835. doi: 10.1038/srep29835.

Abstract

Tyrosine hydroxylase (TH), the initial enzyme in the melanin pathway, catalyzes tyrosine conversion into Dopa. Although expression and regulation of TH have been shown to affect cuticle pigmentation in insects, no direct functional studies to date have focused on the specific physiological processes involving the enzyme during mosquito development. In the current study, silencing of AsTH during the time period of continuous high expression in Anopheles sinensis pupae led to significant impairment of cuticle tanning and thickness, imposing a severe obstacle to eclosion in adults. Meanwhile, deficiency of melanin in interference individuals led to suppression of melanization, compared to control individuals. Consequently, the ability to defend exogenous microorganisms declined sharply. Accompanying down-regulation of the basal expression of five antimicrobial peptide genes resulted in further significant weakening of immunity. TH homologs as well as the composition of upstream transcription factor binding sites at the pupal stage are highly conserved in the Anopheles genus, implying that the TH-mediated functions are crucial in Anopheles. The collective evidence strongly suggests that TH is essential for Anopheles pupae tanning and immunity and provides a reference for further studies to validate the utility of the key genes involved in the melanization pathway in controlling mosquito development.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Anopheles / genetics
  • Anopheles / immunology
  • Anopheles / metabolism*
  • Gene Expression Profiling / methods
  • Insect Proteins / genetics
  • Insect Proteins / metabolism*
  • Melanins / metabolism*
  • Phylogeny
  • Pigmentation / genetics
  • Pupa / genetics
  • Pupa / immunology
  • Pupa / metabolism*
  • RNA Interference
  • Sequence Homology, Amino Acid
  • Tyrosine 3-Monooxygenase / classification
  • Tyrosine 3-Monooxygenase / genetics
  • Tyrosine 3-Monooxygenase / metabolism*

Substances

  • Insect Proteins
  • Melanins
  • Tyrosine 3-Monooxygenase