首页> 外文期刊>Plant methods >Identification of stable reference genes for qPCR studies in common wheat ( Triticum aestivum L.) seedlings under short-term drought stress
【24h】

Identification of stable reference genes for qPCR studies in common wheat ( Triticum aestivum L.) seedlings under short-term drought stress

机译:在短期干旱胁迫下鉴定常见小麦(Triticum Aestivum L.)幼苗QPCR研究的稳定参考基因

获取原文
           

摘要

Quantitative PCR (qPCR) is one of the most common and accurate methods of gene expression analysis. However, the biggest challenge for this kind of examinations is normalization of the results, which requires the application of dependable internal controls. The selection of appropriate reference genes (RGs) is one of the most crucial points in qPCR data analysis and for correct assessment of gene expression. Because of the fact that many reports indicate that the expression profiles of typically used RGs can be unstable in certain experimental conditions, species or tissues, reference genes with stable expression levels should be selected individually for each experiment. In this study, we analysed a set of ten candidate RGs for wheat seedlings under short-term drought stress. Our tests included five ‘traditional’ RGs (GAPDH, ACT, UBI, TUB, and TEF1) and five novel genes developed by the RefGenes tool from the Genevestigator database. Expression stability was assessed using five different algorithms: geNorm, NormFinder, BestKeeper, RefFinder and the delta Ct method. In the final ranking, we identified three genes: CJ705892, ACT, and UBI, as the best candidates for housekeeping genes. However, our data indicated a slight variation between the different algorithms that were used. We revealed that the novel gene CJ705892, obtained by means of in silico analysis, showed the most stable expression in the experimental tissue and condition. Our results support the statement, that novel genes selected for certain experimental conditions have a more stable level of expression in comparison to routinely applied RGs, like genes encoding actin, tubulin or GAPDH. Selected CJ705892 gene can be used as a housekeeping gene in the expression analysis in wheat seedlings under short-term drought. The results of our study will be useful for subsequent analyses of gene expression in wheat tissues subjected to drought.
机译:定量PCR(QPCR)是基因表达分析中最常见和准确的方法之一。然而,这种考试的最大挑战是结果的正常化,这需要应用可靠的内部控制。选择合适的参考基因(RGS)是QPCR数据分析中最关键的点之一,以及对基因表达的正确评估。由于许多报告表明,通常使用的RGS的表达谱在某些实验条件下,物种或组织可以不稳定,但应为每个实验单独选择具有稳定表达水平的参考基因。在这项研究中,我们在短期干旱胁迫下分析了一组用于小麦幼苗的十个候选RG。我们的测试包括五个“传统的”RGS(GAPDH,ACT,UBI,浴缸和TEF1)以及来自Genevistigator数据库的Refgenes工具开发的五种新基因。使用五种不同的算法评估表达稳定性:Genorm,Normfinder,Bestkeeper,Reffinder和Delta CT方法。在最终排名中,我们确定了三个基因:CJ705892,ACT和UBI,作为家务基因的最佳候选人。但是,我们的数据表明使用的不同算法之间的略有变化。我们透露,通过在硅分析中获得的新型基因CJ705892,在实验组织和病症中表达了最稳定的表达。我们的结果支持该陈述,该陈述对于某些实验条件选择的新基因具有更稳定的表达水平,与常规施用的RGS相比,类似于编码肌动蛋白,管蛋白或GAPDH的基因。选择的CJ705892基因可以用作小麦幼苗在短期干旱下表达分析中的家庭基因。我们的研究结果对于随后对经受干旱进行的小麦组织中的基因表达进行后续分析。

著录项

获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号