Microarray analysis reveals strategies of Tribolium castaneum larvae to compensate for cysteine and serine protease inhibitors

Comp Biochem Physiol Part D Genomics Proteomics. 2010 Dec;5(4):280-7. doi: 10.1016/j.cbd.2010.08.001. Epub 2010 Aug 13.

Abstract

The transcriptome response of Tribolium castaneum larvae to dietary protease inhibitors was evaluated by whole-genome microarray analysis. RNA was isolated from guts of larvae fed control diet (no inhibitor), or diets containing 0.1% E-64 (cysteine protease inhibitor), 5.0% soybean trypsin inhibitor (STI, serine protease inhibitor), or a combination of 0.1% E-64 and 5.0% STI. Data were analyzed by pairwise analysis, in which each inhibitor treatment group was compared to control, or ANOVA of all treatment groups. In pairwise analysis, the expression of only 253 genes was significantly altered (p<0.05) in response to STI treatment, whereas E-64 and combination treatments resulted in 1574 and 1584 differentially regulated genes. The data indicate that treatments containing E-64, whether alone or in combination, significantly impacts gene expression in T. castaneum larvae. ANOVA analysis revealed 2175 genes differentially expressed in inhibitor-treated larvae compared to control (p<0.05), including genes related to proteases that were mostly up-regulated, namely cathepsins B and L, chymotrypsins, and nonproteolytic cysteine cathepsin or serine protease homologs. Inhibitor treatments induced the differential expression of other gut-related genes, as well as genes encoding proteins of unknown function. These data suggest that T. castaneum larvae compensate for dietary cysteine protease inhibitors by altering large-scale gene expression patterns.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Chymotrypsin / genetics
  • Chymotrypsin / metabolism
  • Cysteine Proteinase Inhibitors / metabolism
  • Cysteine Proteinase Inhibitors / pharmacology*
  • Drug Combinations
  • Gene Expression Profiling
  • Glycine max / genetics
  • Glycine max / metabolism
  • Larva / metabolism
  • Leucine / analogs & derivatives
  • Leucine / metabolism
  • Leucine / pharmacology
  • Microarray Analysis*
  • Serine Endopeptidases / metabolism
  • Serine Proteinase Inhibitors / metabolism
  • Serine Proteinase Inhibitors / pharmacology*
  • Tribolium / genetics*
  • Tribolium / metabolism*
  • Trypsin Inhibitors / pharmacology

Substances

  • Cysteine Proteinase Inhibitors
  • Drug Combinations
  • Serine Proteinase Inhibitors
  • Trypsin Inhibitors
  • Serine Endopeptidases
  • Chymotrypsin
  • Leucine
  • E 64