Reference gene selection for real-time qPCR in European flounder (Platichthys flesus) using organ-specific RNA-seq data.

IF 2.6 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular Biology Reports Pub Date : 2024-11-21 DOI:10.1007/s11033-024-10105-7
Konrad Pomianowski, Artur Burzyński
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Abstract

Background: The European flounder is readily chosen as an experimental subject and model in physiological and ecotoxicological studies mostly because of its adaptability to laboratory conditions. Many studies utilise a quantitative PCR (qPCR) approach to ascertain the expression of target genes under experimental conditions. Such an approach relies heavily on the selection of reference genes with stable expression. Yet certain housekeeping genes are commonly used in this role, often without due consideration of their overall expression patterns. Therefore, new approaches should be developed to identify stable reference genes for a given species and to expand the general pool of genes suitable for the reference in qPCR analysis.

Methods and results: Here RNA-seq data of nine flounder organs led to identify four candidate genes of the most stable expression. It was achieved by differential expression analysis and tritoconstrictor script. Specific primers were designed for the complete ORF as well as for qPCR analysis. RT-qPCR efficiencies were tested on ORF amplicon templates. Most of the genes tested showed good amplification in a wide range of template dilutions (107-101), with a correlation coefficient (R2) ranging from 0.991 to 0.998 and a consistent efficiency (E) (Sybr Green I staining and TaqMan molecular probe).

Conclusions: The proposed approach based on differential expression analysis and a new bioinformatic tool is an appropriate selection method of candidates for reference genes in qPCR. The proposed approach, combining differential expression analysis with a new bioinformatics tool, provides an effective method for selecting reference gene candidates for qPCR. As a result, we can propose four genes (polr2f, yif1a, sf3b6, uba52), each with a set of validated primers, as suitable for consideration as reference genes in qPCR analysis in European flounder, an emerging model species.

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利用器官特异性 RNA-seq 数据为欧洲比目鱼(Platichthys flesus)的实时 qPCR 选择参考基因。
背景:在生理学和生态毒理学研究中,欧洲比目鱼很容易被选为实验对象和模型,这主要是因为它对实验室条件的适应性很强。许多研究利用定量 PCR(qPCR)方法来确定实验条件下目标基因的表达。这种方法在很大程度上依赖于选择具有稳定表达的参考基因。然而,某些看家基因通常被用来扮演这一角色,而且往往没有充分考虑到它们的整体表达模式。因此,应该开发新的方法来确定特定物种的稳定参考基因,并扩大适合作为 qPCR 分析参考基因的基因库:方法和结果:通过对九个比目鱼器官的 RNA-seq 数据分析,确定了四个表达最稳定的候选基因。这是通过差异表达分析和三缩拮抗剂脚本实现的。为完整的 ORF 以及 qPCR 分析设计了特定引物。在 ORF 扩增片段模板上测试了 RT-qPCR 的效率。大多数受测基因在较宽的模板稀释范围(107-101)内都表现出良好的扩增效果,相关系数(R2)在 0.991 至 0.998 之间,效率(E)一致(Sybr Green I 染色和 TaqMan 分子探针):结论:基于差异表达分析和新的生物信息学工具的拟议方法是在 qPCR 中选择候选参考基因的适当方法。所提出的方法将差异表达分析与一种新的生物信息学工具相结合,为选择 qPCR 的候选参考基因提供了一种有效的方法。因此,我们提出了四个基因(polr2f、yif1a、sf3b6、uba52),每个基因都有一套经过验证的引物,适合作为欧洲鲽(一种新兴模式物种)qPCR 分析的参考基因。
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来源期刊
Molecular Biology Reports
Molecular Biology Reports 生物-生化与分子生物学
CiteScore
5.00
自引率
0.00%
发文量
1048
审稿时长
5.6 months
期刊介绍: Molecular Biology Reports publishes original research papers and review articles that demonstrate novel molecular and cellular findings in both eukaryotes (animals, plants, algae, funghi) and prokaryotes (bacteria and archaea).The journal publishes results of both fundamental and translational research as well as new techniques that advance experimental progress in the field and presents original research papers, short communications and (mini-) reviews.
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