Response of the Pacific oyster Crassostrea gigas to hydrocarbon contamination under experimental conditions

被引:168
作者
Boutet, I [1 ]
Tanguy, A [1 ]
Moraga, D [1 ]
机构
[1] Univ Bretagne Occidentale, Tech Brest Iroise, Inst Univ Europeen Mer, CNRS,UMR 6539,Lab Sci Environm Marin, F-29280 Plouzane, France
关键词
suppression subtractive hybridisation libraries; hydrocarbons; gene expression; detoxification; Crassostrea gigas;
D O I
10.1016/j.gene.2003.12.027
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Hydrocarbon contamination perturbs the metabolism of the marine bivalve Crassostrea gigas. To understand the response of this organism to hydrocarbon exposure, a suppression subtractive hybridisation method was employed to characterise up- and down-regulated genes during hydrocarbon exposure. The number of differentially expressed gene sequences obtained via this method was 258. The expression of genes involved in hydrocarbon detoxification (cytochrome P4501A1-like protein, cytochrome b(5), flavin-containing monooxygenase 2 and glutathione S-transferase omega class), protection against oxidative stress (copper/zinc superoxide dismutase) and cell protection (heat shock protein 70 family) was analysed by RT-PCR. An increase in the mRNA level of all genes studied was observed. A quantification of HSP70 by Enzyme Linked Immunosorbent Assay (ELISA) showed a significant increase of this protein during exposure. This study provides a basis for studying hydrocarbon detoxification processes in marine bivalves, especially C. gigas. (C) 2004 Elsevier B.V All rights reserved.
引用
收藏
页码:147 / 157
页数:11
相关论文
共 38 条
[1]   Enzymatic biomarker measurement and study of DNA adduct formation in benzo[a]pyrene-contaminated mussels, Mytilus galloprovincialis [J].
Akcha, F ;
Izuel, C ;
Venier, P ;
Budzinski, H ;
Burgeot, T ;
Narbonne, JF .
AQUATIC TOXICOLOGY, 2000, 49 (04) :269-287
[2]   ENVIRONMENTAL-STRESS AND OVARIAN-FUNCTION [J].
ARMSTRONG, DT .
BIOLOGY OF REPRODUCTION, 1986, 34 (01) :29-39
[3]   In vitro and in vivo induction of heat shock (stress) protein (Hsp) gene expression by selected pesticides [J].
Bagchi, D ;
Bhattacharya, G ;
Stohs, SJ .
TOXICOLOGY, 1996, 112 (01) :57-68
[4]   Heat shock protein genes and their functional significance in fish [J].
Basu, N ;
Todgham, AE ;
Ackerman, PA ;
Bibeau, MR ;
Nakano, K ;
Schulte, PM ;
Iwama, GK .
GENE, 2002, 295 (02) :173-183
[5]   Analytical procedure for the analysis of PAHs in biological tissues by gas chromatography coupled to mass spectrometry: application to mussels [J].
Baumard, P ;
Budzinski, H ;
Garrigues, P .
FRESENIUS JOURNAL OF ANALYTICAL CHEMISTRY, 1997, 359 (06) :502-509
[6]   The role of non-P450 enzymes in drug oxidation [J].
Beedham, C .
PHARMACY WORLD & SCIENCE, 1997, 19 (06) :255-263
[7]  
Boutet I, 2003, CELL STRESS CHAPERON, V8, P76, DOI 10.1379/1466-1268(2003)8<76:MIAEOH>2.0.CO
[8]  
2
[9]   Identification of differentially expressed genes in Dreissena polymorpha exposed to contaminants [J].
Bultelle, F ;
Panchout, M ;
Leboulenger, F ;
Danger, JM .
MARINE ENVIRONMENTAL RESEARCH, 2002, 54 (3-5) :385-389
[10]   Tissue dose, DNA adducts, oxidative DNA damage and CYP1A-immunopositive proteins in mussels exposed to waterborne benzo[a]pyrene [J].
Canova, S ;
Degan, P ;
Peters, LD ;
Livingstone, DR ;
Voltan, R ;
Venier, P .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 1998, 399 (01) :17-30