Multiple tissue gene expression analyses in Japanese medaka (Oryzias latipes) exposed to hypoxia

Comp Biochem Physiol C Toxicol Pharmacol. 2007 Feb;145(1):134-44. doi: 10.1016/j.cbpc.2006.06.012. Epub 2006 Jun 30.

Abstract

Due in part to human population growth watersheds and coastal estuaries have been receiving increasing run-off of nutrients and genotoxins. As a consequence, the occurrences of nutrient-driven hypoxia in coastal waters appear to be increasing. Thus, understanding the molecular genetic response to hypoxia by model aquatic organisms is of interest both from environmental and physiological viewpoints. The major objectives of this study are to determine genome-wide gene expression profiles and to better understand how hypoxia influences global gene expression in medaka (Oryzias latipes), a well utilized aquatic model species. Herein we detail our development of a microarray containing 8046 medaka unigenes and describe our experimental results for measuring gene expression changes in the brain, gill, and liver of hypoxia exposed fish. Using conservative selection criteria, we determined that 501 genes in the brain, 442 in the gill, and 715 in the liver were differentially expressed in medaka exposed to hypoxia. These differentially expressed genes fell into a number of biological gene ontology groups related to general metabolism, catabolism, RNA and protein metabolism, etc. Two biological pathways, ubiquitin-proteasome and phosphatidylinositol signaling, were significantly dysregulated in medaka upon hypoxia exposure. Comparative genomics between medaka and human identified several human orthologies associated with known diseases.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Brain / metabolism
  • Brain / pathology
  • Brain Chemistry / genetics
  • Gene Expression*
  • Gills / chemistry
  • Gills / metabolism
  • Gills / pathology
  • Hypoxia / genetics*
  • In Situ Hybridization
  • Liver / chemistry
  • Liver / metabolism
  • Liver / pathology
  • Molecular Sequence Data
  • Multigene Family
  • Oligonucleotide Array Sequence Analysis
  • Oligonucleotide Probes
  • Oryzias / genetics*
  • Phosphatidylinositols / physiology
  • RNA / biosynthesis
  • RNA / isolation & purification
  • Reproducibility of Results
  • Reverse Transcriptase Polymerase Chain Reaction
  • Signal Transduction / physiology
  • Ubiquitin / physiology

Substances

  • Oligonucleotide Probes
  • Phosphatidylinositols
  • Ubiquitin
  • RNA