DNA microarray analysis on gene candidates possibly related to tetrodotoxin accumulation in pufferfish

Toxicon. 2014 Jan:77:68-72. doi: 10.1016/j.toxicon.2013.10.030. Epub 2013 Nov 7.

Abstract

Pufferfish accumulate tetrodotoxin (TTX) at high levels in liver and ovary through the food chain. However, the mechanisms underlying TTX toxification in pufferfish have been poorly understood. In order to search gene candidates involved in TTX accumulation in the torafugu pufferfish Takifugu rubripes, a custom 4x44k oligonucleotide microarray slide was designed by the Agilent eArray program using oligonucleotide probes of 60 bp in length referring to 42,724 predicted transcripts in the publicly available Fugu genome database. DNA microarray analysis was performed with total RNA samples from the livers of two toxic wild specimens in comparison with those from a nontoxic wild specimen and two nontoxic cultured specimens. The mRNA levels of 1108 transcripts were more than 2-fold higher in the toxic specimens than in the nontoxic specimens. The levels of 613 transcripts were remarkably high, and 16 transcripts encoded by 9 genes were up-regulated more than 10-fold. These genes included those encoding forming structural filaments (keratins) and those related to vitamin D metabolism and immunity. It was also noted that the levels of the transcripts encoding serpin peptidase inhibitor clade C member 1, coagulation factor X precursor, complement C2, C3, C5, C8 precursors, and interleukin-6 receptor were high in the toxic liver samples.

Keywords: APP; DNA microarray; Gene expression; IL-6; Keratin; LC–FLD; Pufferfish; RAP RT–PCR; SSH; TTX; Takifugu rubripes; Tetrodotoxin; acute phase protein; fibrinogen-like protein; flp; interleukin-6; liquid chromatography–fluorescence detection; mRNA arbitrarily primed reverse transcription–polymerase chain reaction; suppression subtractive hybridization; tetrodotoxin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antithrombin III / metabolism
  • Complement System Proteins / metabolism
  • Factor X / metabolism
  • Fishes, Poisonous / genetics*
  • Fishes, Poisonous / metabolism
  • Gene Expression Regulation / physiology*
  • Japan
  • Keratins / metabolism
  • Liver / metabolism
  • Oligonucleotide Array Sequence Analysis / methods
  • Oligonucleotide Probes
  • Receptors, Interleukin-6 / metabolism
  • Tetraodontiformes / genetics*
  • Tetraodontiformes / metabolism
  • Tetrodotoxin / metabolism*
  • Tetrodotoxin / pharmacokinetics*
  • Vitamin D / metabolism

Substances

  • Oligonucleotide Probes
  • Receptors, Interleukin-6
  • Vitamin D
  • Tetrodotoxin
  • Keratins
  • Antithrombin III
  • Factor X
  • Complement System Proteins