Suppression subtractive hybridization cDNA libraries to identify differentially expressed genes from contrasting fish habitats

Mar Biotechnol (NY). 2004 Jul-Aug;6(4):386-99. doi: 10.1007/s10126-004-3146-6. Epub 2004 Aug 6.

Abstract

Suppression subtractive hybridization complementary DNA libraries identified differentially expressed genes in liver tissue of winter flounder collected from the highly impacted Raritan-Hudson estuary versus those from less industrialized estuaries farther south in New Jersey. Distinct transcript profiles emerged in the fish from these different habitats. A total of 251 clones from the forward (upregulated with anthropogenic impact) and reverse (downregulated with anthropogenic impact) subtracted libraries were sequenced. In the upregulated library immune response transcripts, including complement C-3, C-7, factor H, factor Bf/C2, differentially regulated trout protein 1, and the antimicrobial hepcidin, indicated the pollution-impacted fish were under a high viral or bacterial load. Transcripts for cytochrome P450 1A, P450 3A, and glutathione S-transferase, important components of phase I and II metabolism of xenobiotics, were found in the upregulated-with-pollution library. Vitellogenins I and II and egg envelope protein (zp) appeared to be downregulated. A homologue of the tumor suppressor p33(ING1) (down) and hepatocyte growth factor-like protein (up) may indicate liver damage or hepatocellular carcinoma or hepatoma. These expression patterns, confirmed by quantitative polymerase chain reaction, indicate that transcript analysis is a useful method for assessing the health of local habitats and the organisms therein.

Publication types

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

MeSH terms

  • Animals
  • Base Sequence
  • DNA Primers
  • Environment*
  • Flounder / genetics*
  • Flounder / metabolism
  • Gene Expression Regulation*
  • Gene Library
  • Genetic Markers / genetics
  • Liver / metabolism*
  • Molecular Sequence Data
  • New Jersey
  • Nucleic Acid Hybridization / methods
  • Polymerase Chain Reaction / methods
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sequence Analysis, DNA
  • Water Pollution, Chemical*

Substances

  • DNA Primers
  • Genetic Markers