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A real-time PCR assay for differential expression of vitellogenin i and II genes in the liver of the sentinel fish species Lipophrys pholis

机译:实时PCR检测前哨鱼类Lipophrys pholis肝脏中卵黄蛋白原i和II基因的差异表达

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摘要

The recent advances in molecular biology techniques have prompted the use of vitellogenin (VTG) gene expression as a sensitive and reliable indicator of estrogenic chemicals (EC) exposure. However, data on the dynamic response of the different VTGs genes upon EC exposure is still poorly understood, particularly in sentinel fish species used in field monitoring studies. Hence, the present study aimed at developing a sensitive real-time PCR assay for determining the response of VTG I and II in the recently proposed marine sentinel species Lipophrys pholis upon exposure to the model EC 17α-ethinylestradiol (EE2). The findings of the laboratory study indicate that L. pholis VTG I proved to be not only more inducible but also more sensitive to EE2 exposure than VTG II, for the same range of concentrations. In fact, VTG I gene induction was 475-fold higher than VTG II at 15ng/L EE2, and 13-fold at 5ng/L EE2. Overall, the findings of the present study indicate that in the field, expression of VTG I in L. pholis should be preferentially used in the screening of EC exposure because of its higher sensitivity. Furthermore, the present study favors L. pholis integration in monitoring programs associated with EC's pollution within the European water policy legislation.
机译:分子生物学技术的最新进展已促使使用卵黄蛋白原(VTG)基因表达作为雌激素化学物质(EC)暴露的灵敏可靠的指标。但是,关于EC暴露时不同VTG基因动态响应的数据仍然知之甚少,特别是在田间监测研究中使用的前哨鱼类中。因此,本研究旨在开发一种灵敏的实时PCR分析方法,用于确定最近提出的海洋前哨物种Lipophrys pholis在暴露于EC17α-炔雌醇(EE2)时的VTG I和II响应。实验室研究的结果表明,在相同的浓度范围内,相比于VTG II,L。pholis VTG I不仅对V2更具诱导性,而且对EE2的暴露更为敏感。实际上,在15ng / L EE2时,VTG I基因诱导比VTG II高475倍,在5ng / L EE2时是13倍。总体而言,本研究的结果表明,在野外,由于在L. pholis中的VTG I表达具有较高的敏感性,因此应优先用于EC暴露的筛选。此外,本研究支持在欧洲水政策法规范围内将L. pholis整合到与EC污染相关的监测程序中。

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