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高通量 cDNA 测序揭示慢性金属暴露对野生鱼类种群的影响。

Effects of chronic metal exposure on wild fish populations revealed by high-throughput cDNA sequencing.

机构信息

Institut National de La Recherche Scientifique, INRS-Centre Eau Terre Environnement, 490 de la Couronne, Quebec, QC, G1K 9A9, Canada.

出版信息

Ecotoxicology. 2011 Aug;20(6):1388-99. doi: 10.1007/s10646-011-0696-z. Epub 2011 May 10.

Abstract

Given the inherent variability of aquatic systems, predicting the in situ effects of contaminants on such ecosystems still represents a major challenge for ecotoxicology. In this context, transcriptomic tools can help identify and investigate the mechanisms of toxicity beyond the traditional morphometric, physiological and population-level endpoints. In this study, we used the 454 sequencing technology to examine the in situ effects of chronic metal (Cd, Cu) exposure on the yellow perch (Perca flavescens) transcriptome. Total hepatic mRNA from fish sampled along a polymetallic gradient was extracted, reverse transcribed, labeled with unique barcode sequences and sequenced. This approach allowed us to identify correlations between the transcription level of single genes and the hepatic concentrations of individual metals; 71% of the correlations established were negative. Chronic metal exposure was thus associated with a decrease in the transcription levels of numerous genes involved in protein biosynthesis, in the immune system, and in lipid and energy metabolism. Our results suggest that this marked decrease could result from an impairment of bile acid metabolism by Cd and energy restriction but also from the recruitment of several genes involved in epigenetic modifications of histones and DNA that lead to gene silencing.

摘要

鉴于水生系统固有的变异性,预测污染物对这些生态系统的原位影响仍然是生态毒理学的一个主要挑战。在这种情况下,转录组学工具可以帮助识别和研究毒性机制,超越传统的形态、生理和种群水平终点。在这项研究中,我们使用 454 测序技术来研究慢性金属(Cd、Cu)暴露对黄鲈(Perca flavescens)转录组的原位影响。从沿多金属梯度采集的鱼类肝脏中提取总 mRNA,反转录,用独特的条形码序列标记并测序。这种方法使我们能够识别单个基因转录水平与单个金属肝脏浓度之间的相关性;建立的相关性中有 71%是负相关的。因此,慢性金属暴露与参与蛋白质生物合成、免疫系统以及脂质和能量代谢的许多基因的转录水平下降有关。我们的结果表明,这种明显的下降可能是由于 Cd 破坏了胆汁酸代谢和能量限制,也可能是由于招募了几个参与组蛋白和 DNA 表观遗传修饰的基因,导致基因沉默。

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