Department of Entomology, South China Agricultural University, Guangzhou, Guangdong, People's Republic China.
PLoS One. 2013;8(2):e57718. doi: 10.1371/journal.pone.0057718. Epub 2013 Feb 28.
To accurately assess gene expression levels, it is essential to normalize real-time quantitative PCR (RT-qPCR) data with suitable internal reference genes. For the red imported fire ant, Solenopsis invicta, reliable reference genes to assess the transcript expression levels of the target genes have not been previously investigated. In this study, we examined the expression levels of five candidate reference genes (rpl18, ef1-beta, act, GAPDH, and tbp) in different developmental stages, castes and tissues of S. invicta. To evaluate the suitability of these genes as endogenous controls, three software-based approaches (geNorm, BestKeeper and NormFinder) and one web-based comprehensive tool (RefFinder) were used to analyze and rank the tested genes. Furthermore, the optimal number of reference gene(s) was determined by the pairwise variation value. Our data showed that two of the five candidate genes, rpl18 and ef1-beta, were the most suitable reference genes because they have the most stable expression among different developmental stages, castes and tissues in S. invicta. Although widely used as reference gene in other species, in S. invicta the act gene has high variation in expression and was consequently excluded as a reliable reference gene. The two validated reference genes, rpl18 and ef1-beta, can be widely used for quantification of target gene expression with RT-qPCR technology in S. invicta.
为了准确评估基因表达水平,必须使用合适的内参基因对实时定量 PCR(RT-qPCR)数据进行标准化。对于红火蚁,红火蚁 Solenopsis invicta,尚未对评估靶基因转录表达水平的可靠参考基因进行研究。在这项研究中,我们检测了 5 种候选参考基因(rpl18、ef1-β、act、GAPDH 和 tbp)在不同发育阶段、性别和组织中的表达水平。为了评估这些基因作为内参的适用性,使用了三种基于软件的方法(geNorm、BestKeeper 和 NormFinder)和一种基于网络的综合工具(RefFinder)来分析和对测试基因进行排名。此外,通过成对差异值确定最佳参考基因(s)的数量。我们的数据表明,在 S. invicta 中,这 5 个候选基因中的两个,rpl18 和 ef1-β,是最适合的参考基因,因为它们在不同的发育阶段、性别和组织中具有最稳定的表达。尽管在其他物种中广泛用作参考基因,但在 S. invicta 中,act 基因的表达变化很大,因此不能作为可靠的参考基因。这两个经过验证的参考基因 rpl18 和 ef1-β 可以广泛用于使用 RT-qPCR 技术对 S. invicta 中的靶基因表达进行定量。