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首页> 外文期刊>BMC Genomics >Identification of two putative reference genes from grapevine suitable for gene expression analysis in berry and related tissues derived from RNA-Seq data
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Identification of two putative reference genes from grapevine suitable for gene expression analysis in berry and related tissues derived from RNA-Seq data

机译:从葡萄中鉴定出两个推定的参考基因,这些参考基因适用于从RNA-Seq数据得出的浆果和相关组织中的基因表达分析

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摘要

Background Data normalization is a key step in gene expression analysis by qPCR. Endogenous control genes are used to estimate variations and experimental errors occurring during sample preparation and expression measurements. However, the transcription level of the most commonly used reference genes can vary considerably in samples obtained from different individuals, tissues, developmental stages and under variable physiological conditions, resulting in a misinterpretation of the performance of the target gene(s). This issue has been scarcely approached in woody species such as grapevine. Results A statistical criterion was applied to select a sub-set of 19 candidate reference genes from a total of 242 non-differentially expressed (NDE) genes derived from a RNA-Seq experiment comprising ca. 500 million reads obtained from 14 table-grape genotypes sampled at four phenological stages. From the 19 candidate reference genes, VvAIG1 (AvrRpt2-induced gene) and VvTCPB (T-complex 1 beta-like protein) were found to be the most stable ones after comparing the complete set of genotypes and phenological stages studied. This result was further validated by qPCR and geNorm analyses. Conclusions Based on the evidence presented in this work, we propose to use the grapevine genes VvAIG1 or VvTCPB or both as a reference tool to normalize RNA expression in qPCR assays or other quantitative method intended to measure gene expression in berries and other tissues of this fruit crop, sampled at different developmental stages and physiological conditions.
机译:背景数据标准化是通过qPCR进行基因表达分析的关键步骤。内源性对照基因用于估计样品制备和表达测量过程中发生的变异和实验错误。然而,在从不同的个体,组织,发育阶段以及在可变的生理条件下获得的样品中,最常用的参考基因的转录水平可以有很大的不同,从而导致对靶基因的性能的误解。在诸如葡萄树这样的木本物种中几乎没有解决这个问题。结果应用统计学标准从总共242个非差动表达(NDE)基因中选择19个候选参考基因的子集,该基因由包含ca.的RNA-Seq实验衍生而来。从四个物候阶段采样的14种表型葡萄基因型获得5亿条读数。在比较了完整的基因型和物候阶段后,从19个候选参考基因中,发现VvAIG1(AvrRpt2诱导的基因)和VvTCPB(T型复合物1β样蛋白)是最稳定的。通过qPCR和geNorm分析进一步验证了该结果。结论基于这项工作中提出的证据,我们建议使用葡萄基因VvAIG1或VvTCPB或两者均作为参考工具,以在qPCR分析或旨在定量该果实的浆果和其他组织中的基因表达的其他定量方法中标准化RNA表达。作物,在不同的发育阶段和生理条件下取样。

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