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A DNA expression array to detect toxic stress response in European flounder (Platichthys flesus)
Williams, T.D.; Gensberg, K.; Minchin, S.D.; Chipman, J.K. (2003). A DNA expression array to detect toxic stress response in European flounder (Platichthys flesus). Aquat. Toxicol. 65(2): 141-157. https://dx.doi.org/10.1016/S0166-445X(03)00119-X
In: Aquatic Toxicology. Elsevier Science: Tokyo; New York; London; Amsterdam. ISSN 0166-445X; e-ISSN 1879-1514, more
Peer reviewed article  

Available in  Authors 

Keywords
    Acids > Organic compounds > Organic acids > Nucleic acids > DNA
    Arrays
    Cdna array
    Chordata > Vertebrates > Fishes > Osteichthyes > Pleuronectiformes > Marine fishes > Flounder
    Disciplines > Biology > Molecular biology > Genetics > Genomics > Functional genomics > Toxicology > Toxicogenomics
    Gene expression
    Polymerase chain reaction
    Toxicology
    Platichthys flesus (Linnaeus, 1758) [WoRMS]
    ANE, British Isles, England, Tyne and Wear, Tyne E [Marine Regions]
    Marine/Coastal

Authors  Top 
  • Williams, T.D., correspondent
  • Gensberg, K.
  • Minchin, S.D.
  • Chipman, J.K.

Abstract
    As a first stage in developing a DNA array-based approach to investigating the effects of pollutants on an environmentally relevant European fish species, we have constructed a 160-gene custom microarray for European flounder. Degenerate primers were used to amplify 110 different fragments of stress-related and other genes from European flounder cDNA and genomic DNA. Additionally, 22 fragments were obtained by suppressive subtractive hybridisation (SSH). These fragments were cloned and sequenced, then, with additional control genes, used to create a cDNA microarray for flounder. After optimisation of the arraying process, hepatic mRNA was isolated from flounder caught in the polluted Tyne and relatively unpolluted Alde estuaries. Fluorescent cDNA probes were synthesised from the mRNA and used in dual-colour hybridisations to the microarray. A number of transcripts were differentially expressed between Tyne and Alde female flounder but these changes were not significant, due to high inter-individual variation. However, in comparisons between Tyne and Alde male flounder, 11 transcripts were found to significantly differ in expression (P < 0.05). Seven transcripts were more highly expressed in the Tyne male fish (CYP1A, UDPGT, α-2HS-glycoprotein, dihydropyrimidine dehydrogenase, Cu/Zn SOD, aldehyde dehydrogenase and paraoxonase). Four transcripts (Elongation factor 1 (EF1), EF2, Int-6 and complement component C3) were found to be significantly less abundant in the Tyne male fish. Selected genes were assayed by real-time PCR, then normalised to α-tubulin. These assays confirmed the significance of the array results for CYP1A, UDPGT and EF1, but not for Cu/Zn SOD. This study provides a link between traditional single-gene biomarker studies and the emerging field of eco-toxicogenomics, demonstrating the utility of microarray studies on environmentally sampled, non-model organisms.

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