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Effects of cadmium exposure on sea urchin development assessed by SSH and RT-qPCR: metallothionein genes and their differential induction

机译:SSH和RT-qPCR评估镉暴露对海胆发育的影响:金属硫蛋白基因及其差异诱导

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In order to study the defense strategies activated by Paracentrotus lividus embryos in response to sub-lethal doses of CdCl2, we compared the induced transcripts to that of control embryos by suppression subtractive hybridization technique. We isolated five metallothionein (MT) cDNAs and other genes related to detoxification, to signaling pathway components, to oxidative, reductive and conjugative biotransformation, to RNA maturation and protein synthesis. RT-qPCR analysis revealed that two of the five P. lividus MT (PlMT7 and PlMT8) genes appeared to be constitutively expressed and upregulated following cadmium treatment, whereas the other three genes (PlMT4, PlMT5, PlMT6) are specifically switched-on in response to cadmium treatment. Moreover, we found that this transcriptional induction is concentration dependent and that the cadmium concentration threshold for the gene activation is distinct for every gene. RT-qPCR experiments showed in fact that, among induced genes, PlMT5 gene is activated at a very low cadmium concentration (0.1 μM) whereas PlMT4 and PlMT6 are activated at intermediate doses (1–10 μM). Differently, PlMT7 and PlMT8 genes increase significantly their expression only in embryos treated with the highest dose (100 μM CdCl2). We found also that, in response to a lethal dose of cadmium (1 μM), only PlMT5 and PlMT6 mRNA levels increased further. These data suggest a hierarchical and orchestrated response of the P. lividus embryo to overcome differential environmental stressors that could interfere with a normal development.
机译:为了研究Paracentrotus lividus胚胎针对亚致死剂量的CdCl2激活的防御策略,我们通过抑制消减杂交技术将诱导的转录本与对照胚胎的转录本进行了比较。我们分离了五个金属硫蛋白(MT)cDNA和其他与解毒,信号通路成分,氧化,还原和结合生物转化,RNA成熟和蛋白质合成有关的基因。 RT-qPCR分析显示,五个C.lividus MT基因(PlMT7和PlMT8)中的两个似乎在镉处理后组成性表达和上调,而其他三个基因(PlMT4,PlMT5,PlMT6)在响应中被特异性开启去镉治疗。此外,我们发现这种转录诱导是浓度依赖性的,并且对于每个基因而言,基因激活的镉浓度阈值是不同的。 RT-qPCR实验实际上表明,在诱导基因中,PlMT5基因在非常低的镉浓度(0.1μM)下被激活,而PlMT4和PlMT6在中等剂量(1-10μM)下被激活。不同的是,PlMT7和PlMT8基因仅在以最高剂量(100μMCdCl2)处理的胚胎中表达显着增加。我们还发现,响应致命剂量的镉(1μM),只有PlMT5和PlMT6 mRNA水平进一步升高。这些数据表明青紫假单胞菌胚胎的分层和协调响应,以克服可能干扰正常发育的不同环境应激源。

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