4.6 Article

Cloning and expression of a GST-pi gene in Mytilus galloprovincialis.: Attempt to use the GST-pi transcript as a biomarker of pollution

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ELSEVIER SCIENCE INC
DOI: 10.1016/j.cbpc.2006.02.007

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mussels; Mytilus galloprovincialis; glutathione S-transferase; molecular cloning; gene expression; biomarker; chemical pollutants

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Glutathione S-transferase is involved in the detoxication of many chemical compounds. Northern blot analysis of mRNA GST gene from the mussel Mytilus galloprovincialis shows the presence of a transcript of 850bp (GenBank accession no. Gi:22094808 and AF527010). The cDNA cloned sequence is constituted by an ORF of 621 bp encoding for a protein of 23,700 Da present in the gills and digestive gland of M galloprovincialis. The sequence, called Mg (M. galloprovincialis) GST-p, is clearly related to the pi class GST. M galloprovincialis treated with Cd (200 mu g/L) and BaP (100 mu g/L) or co-treated with Cd and BaP take up cadmium in the gills (16.2 +/- 4.2 and 12.6 +/- 1.2 mu g Cd/g dry wt. after exposure to Cd and Cd+BaP, respectively) and in the digestive gland. The transcription of GST-pi gene, by semi-quantitative RT-PCR, shows the lowest value in the digestive glands of mussels exposed to BaP, whereas the treatment with cadmium and the co-treatment with cadmium and BaP evoke GST-pi gene expression higher than controls. Mussels collected from six sites along the south coast of Portugal show different GST-pi transcription levels, some of which are related to their pollutant content. (c) 2006 Elsevier Inc. All rights reserved.

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