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首页> 外文期刊>Journal of Applied Phycology >Transcriptome-wide identification and evaluation of optimal reference genes for RT-qPCR expression analysis of Saccharina latissima responses to biotic and abiotic stress
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Transcriptome-wide identification and evaluation of optimal reference genes for RT-qPCR expression analysis of Saccharina latissima responses to biotic and abiotic stress

机译:用于生物和非生物胁迫的巨曲型抗胰岛素响应的RT-QPCR表达分析的转录组宽鉴定与评价

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Saccharina latissima, known as sugar kelp, is a brown macroalga with huge ecological and economic values. In marine intertidal environment, S. latissima has to cope with both biotic and abiotic stress, which can cause the reduction of the yield during cultivation. To better understand the physiological responses of S. latissima under different stress conditions, large-scale transcriptomic analyses are useful to explore global metabolic pathway regulations. In addition, real-time quantitative polymerase chain reaction (RT-qPCR) is a powerful and rapid method for further quantifying changes in gene expression, and for targeting specific defense-related gene pathways. However, its level of accuracy is highly related to the expression stability of reference genes used for normalization and those still need to be evaluated in S. latissima. In this study, we therefore experimentally tested eight candidate reference genes identified from in silico screening of public transcriptomic datasets of S. latissima from different abiotic and biotic stress treatments. The stability analysis using complementary statistical approaches showed that EIF5B and ATPase are the most stable reference genes under biotic stress, whereas, under temperature and light stress, their combination with NDH gene is the best choice for RT-qPCR normalization. The validated reference genes were used to monitor the expression of target genes, related to oxidative responses, such as those involved in oxylipin pathways, in S. latissima plantlets submitted to different stress in laboratory-controlled conditions.
机译:糖藻(Saccharina latissima)是一种具有巨大生态和经济价值的棕色大型海藻,又名糖带。在海洋潮间带环境中,宽鳍金枪鱼必须同时应对生物和非生物胁迫,这可能导致养殖期间产量下降。为了更好地了解宽吻链球菌在不同应激条件下的生理反应,大规模转录组学分析有助于探索整体代谢途径调控。此外,实时定量聚合酶链反应(RT-qPCR)是进一步量化基因表达变化和针对特定防御相关基因途径的一种强大而快速的方法。然而,其准确性水平与用于标准化的参考基因的表达稳定性高度相关,这些基因仍需在宽吻链球菌中进行评估。因此,在这项研究中,我们对八个候选参考基因进行了实验测试,这些候选参考基因是从不同非生物和生物胁迫处理的宽吻链球菌公开转录组数据集中的电子筛选中确定的。利用互补统计方法进行的稳定性分析表明,EIF5B和ATP酶是生物胁迫下最稳定的参考基因,而在温度和光照胁迫下,它们与NDH基因的结合是RT-qPCR标准化的最佳选择。在实验室控制的条件下,将验证的参考基因用于监测与氧化反应相关的靶基因的表达,例如参与氧化脂质途径的靶基因,这些靶基因在提交给不同应激的宽吻链球菌植株中的表达。

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