Lü Jing, Yang Chunxiao, Zhang Youjun, Pan Huipeng
Key Laboratory of Bio-Pesticide Innovation and Application of Guangdong Province, Department of Entomology, South China Agricultural University, Guangzhou, China.
State Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources, South China Agricultural University, Guangzhou, China.
Front Physiol. 2018 Nov 6;9:1560. doi: 10.3389/fphys.2018.01560. eCollection 2018.
Reverse transcriptase-quantitative polymerase chain reaction (RT-qPCR) is a reliable technique for quantifying expression levels of targeted genes during various biological processes in numerous areas of clinical and biological research. Selection of appropriate reference genes for RT-qPCR normalization is an elementary prerequisite for reliable measurements of gene expression levels. Here, by analyzing datasets published between 2008 and 2017, we summarized the current trends in reference gene selection for insect gene expression studies that employed the most widely used SYBR Green method for RT-qPCR normalization. We curated 90 representative papers, mainly published in 2013-2017, in which a total of 78 insect species were investigated in 100 experiments. Furthermore, top five journals, top 10 frequently used reference genes, and top 10 experimental factors have been determined. The relationships between the numbers of the reference genes, experimental factors, analysis tools on the one hand and publication date (year) on the other hand was investigated by linear regression. We found that the more recently the paper was published, the more experimental factors it tended to explore, and more analysis tools it used. However, linear regression analysis did not reveal a significant correlation between the number of reference genes and the study publication date. Taken together, this meta-analysis will be of great help to researchers that plan gene expression studies in insects, especially the non-model ones, as it provides a summary of appropriate reference genes for expression studies, considers the optimal number of reference genes, and reviews the average number of experimental factors and analysis tools per study.
逆转录定量聚合酶链反应(RT-qPCR)是一种可靠的技术,可用于量化临床和生物学研究众多领域中各种生物过程中靶向基因的表达水平。选择合适的内参基因进行RT-qPCR标准化是可靠测量基因表达水平的基本前提。在此,通过分析2008年至2017年间发表的数据集,我们总结了采用最广泛使用的SYBR Green方法进行RT-qPCR标准化的昆虫基因表达研究中内参基因选择的当前趋势。我们筛选了90篇代表性论文,主要发表于2013年至2017年,其中在100项实验中总共研究了78种昆虫。此外,还确定了排名前五的期刊、十大常用内参基因和十大实验因素。通过线性回归研究了内参基因数量、实验因素、分析工具与发表日期(年份)之间的关系。我们发现,论文发表的时间越近,它倾向于探索的实验因素就越多,使用的分析工具也越多。然而,线性回归分析并未揭示内参基因数量与研究发表日期之间的显著相关性。综上所述,这项荟萃分析将对计划进行昆虫基因表达研究的研究人员,尤其是非模式昆虫的研究人员有很大帮助,因为它提供了表达研究的合适内参基因总结,考虑了内参基因的最佳数量,并回顾了每项研究的实验因素和分析工具的平均数量。