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首页> 外文期刊>BMC research notes >Validation of reference genes for quantitative RT-qPCR studies of gene expression in Atlantic cod (Gadus morhua l.) during temperature stress
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Validation of reference genes for quantitative RT-qPCR studies of gene expression in Atlantic cod (Gadus morhua l.) during temperature stress

机译:验证参考基因的定量RT-qPCR研究温度胁迫下大西洋鳕(Gadus morhua l。)中基因表达

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Background One important physiological response to environmental stress in animals is change in gene expression. To obtain reliable data from gene expression studies using RT-qPCR it is important to evaluate a set of possible reference genes as normalizers for expression. The expression of these candidate genes should be analyzed in the relevant tissues during normal and stressed situations. To find suitable reference genes it was crucial that the genes were stably expressed also during a situation of physiological stress. For poikilotermic animals like cod, changes in temperature are normal, but if the changes are faster than physiological compensation, the animals respond with typical stress responses. It has previously been shown that Atlantic cod show stress responses when elevation of water temperature is faster than 1 degree/day, for this reason we chose hyperthermia as stress agent for this experiment. Findings We here describe the expression of eight candidate reference genes from Atlantic cod ( Gadus morhua l .) and their stability during thermal stress (temperature elevation of one degree C/day for 5 days). The genes investigated were: Eukaryotic elongation factor 1 alpha, ef1a ; 18s ribosomal RNA; 18s , Ubiquitin conjugate protein; ubiq , cytoskeletal beta-actin; actb , major histcompatibility complex I; MHC-I light chain, beta-2 -microglobulin; b2m , cytoskeletal alpha-tubulin; tba1c , acidic ribosomal phosphoprotein; rplp1 , glucose-6-phosphate dehydrogenase; g6pd . Their expression were analyzed in 6 tissues (liver, head kidney, intestine, spleen, heart and gills) from cods exposed to elevated temperature and compared to a control group. Although there were variations between tissues with respect to reference gene stability, four transcripts were more consistent than the others: ubiq , ef1a , 18s and rplp1 . We therefore used these to analyze the expression of stress related genes (heat shock proteins) induced during hyperthermia. We found that both transcripts were significantly upregulated in several tissues in fish exposed to increased temperature. Conclusion This is the first study comparing reference genes for RT-qPCR analyses of expression during hyperthermia in Atlantic cod. ef1a, 18s, rplp1 and ubiq transcripts were found to be well suited as reference genes during these experimental conditions.
机译:背景技术对动物环境压力的一种重要的生理反应是基因表达的改变。为了从使用RT-qPCR进行的基因表达研究中获得可靠的数据,重要的是评估一组可能的参考基因作为表达的标准化子。在正常和压力情况下,应在相关组织中分析这些候选基因的表达。为了找到合适的参考基因,至关重要的是这些基因在生理压力下也要稳定表达。对于像鳕鱼这样的足白蚁动物,温度变化是正常的,但是如果变化快于生理补偿,则动物会产生典型的应激反应。先前已经证明,当水温升高速度超过1度/天时,大西洋鳕鱼会显示出压力响应,因此,我们选择高温作为本实验的压力因子。研究结果我们在此描述了来自大西洋鳕(Gadus morhua l。)的八个候选参考基因的表达及其在热胁迫期间的稳定性(温度升高1摄氏度/天,持续5天)。研究的基因是:真核延伸因子1α,ef1a; 18s核糖体RNA; 18s,泛素结合蛋白;泛素,细胞骨架β-肌动蛋白; actb,主要组织相容性复合体I; MHC-1轻链,β2-微球蛋白; b2m,细胞骨架α-微管蛋白; tba1c,酸性核糖体磷蛋白; rplp1,6-磷酸葡萄糖脱氢酶; g6pd。分析了暴露于高温的鳕鱼在6个组织(肝,头肾,肠,脾,心脏和g)中的表达,并与对照组进行了比较。尽管组织之间在参考基因稳定性方面存在差异,但四个转录物比其他转录物更一致:ubiq,ef1a,18s和rplp1。因此,我们使用这些分析热疗过程中诱导的应激相关基因(热激蛋白)的表达。我们发现暴露于升高温度的鱼的两个组织中的两个转录本均显着上调。结论这是第一项比较参考基因用于RT-qPCR分析大西洋鳕鱼热疗过程中表达的研究。在这些实验条件下,发现ef1a,18s,rplp1和ubiq转录本非常适合作为参考基因。

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