Centre for Environment, Fisheries and Aquaculture Science, Cefas Weymouth Laboratory, Weymouth, Dorset, UK.
Aquat Toxicol. 2010 May 5;97(3):174-87. doi: 10.1016/j.aquatox.2009.07.005. Epub 2009 Jul 17.
An established three-spined stickleback (Gasterosteus aculeatus) cDNA array was expanded to 14,496 probes with the addition of hepatic clones derived from subtractive and normalized libraries from control males and males exposed to model toxicants. Microarrays and one-dimensional (1)H nuclear magnetic resonance (NMR) spectroscopy, together with individual protein and gene biomarkers were employed to investigate the hepatic responses of the stickleback to ethinyl-estradiol (EE(2)) exposure. Male fish were exposed via the water to EE(2), including environmentally relevant concentrations (0.1-100ng/l) for 4 days, and hepatic transcript and metabolite profiles, kidney spiggin protein and serum vitellogenin concentrations were determined in comparison to controls. EE(2) exposure did not significantly affect spiggin concentration but significantly induced serum vitellogenin protein at the threshold concentration of 32ng/l. (1)H NMR coupled with robust univariate testing revealed only limited changes, but these did support the predicted modulation of the amino acid profile by transcriptomics. Transcriptional induction was found for hepatic vitellogenins and choriogenins as expected, together with a range of other EE(2)-responsive genes. Choriogenins showed the more sensitive responses with statistically significant induction at 10ng/l. Real-time polymerase chain reaction (PCR) confirmed transcriptional induction of these genes. Phosvitinless vitellogenin C transcripts were highly expressed and represent a major form of the egg yolk precursors, and this is in contrast to other fish species where it is a minor component of vitellogenic transcripts. Differences in inducibility between the vitellogenins and choriogenins appear to be in accordance with the sequential formation of chorion and yolk during oogenesis in fish.
建立了一个三刺棘鱼(Gasterosteus aculeatus)cDNA 芯片,该芯片扩展到 14496 个探针,其中包括从对照雄性和暴露于模型毒物的雄性肝脏中衍生的消减和标准化文库的克隆。微阵列和一维(1)H 核磁共振(NMR)光谱以及个体蛋白和基因生物标志物一起用于研究棘鱼肝脏对雌二醇(EE(2))暴露的反应。雄性鱼通过水暴露于 EE(2)中,包括环境相关浓度(0.1-100ng/l)4 天,并与对照相比测定肝脏转录物和代谢物谱、肾脏 spiggin 蛋白和血清卵黄蛋白原浓度。EE(2)暴露没有显著影响 spiggin 浓度,但在 32ng/l 的阈值浓度下显著诱导血清卵黄蛋白原蛋白。(1)H NMR 与强大的单变量测试相结合仅显示出有限的变化,但这些变化确实支持了转录组学对氨基酸谱的预测调节。如预期的那样,肝脏卵黄蛋白原和卵黄蛋白原以及一系列其他 EE(2)反应基因的转录诱导。卵黄蛋白原显示出更敏感的反应,在 10ng/l 时具有统计学意义的诱导。实时聚合酶链反应(PCR)证实了这些基因的转录诱导。无磷卵黄蛋白原 C 转录物高度表达,代表卵黄前体的主要形式,与其他鱼类物种形成鲜明对比,在其他鱼类物种中,它是卵黄生成转录物的次要成分。卵黄蛋白原和卵黄蛋白原之间的诱导能力差异似乎与鱼类卵子发生过程中卵黄和卵黄的顺序形成一致。